Difference between revisions of "Team:XMU-China/Hardware"

Line 1: Line 1:
<!DOCTYPE html>
 
 
<html lang="en">
 
<html lang="en">
  
Line 23: Line 22:
 
     <meta name="x5-page-mode" content="app"><!-- QQ应用模式 -->
 
     <meta name="x5-page-mode" content="app"><!-- QQ应用模式 -->
 
     <meta name="msapplication-tap-highlight" content="no"><!-- windows phone 点击无高光 -->
 
     <meta name="msapplication-tap-highlight" content="no"><!-- windows phone 点击无高光 -->
     <title>Team:XMU-China/Description - 2018.igem.org</title>
+
     <title>Team:XMU-China/Hardware - 2018.igem.org</title>
     <link rel="stylesheet" href="css/desciption.css">
+
     <link rel="stylesheet" href="css/interlab.css">
 +
    <link rel="stylesheet" href="css/font.css">
 
     <link href="http://cdn.bootcss.com/font-awesome/4.7.0/css/font-awesome.min.css" rel="stylesheet">
 
     <link href="http://cdn.bootcss.com/font-awesome/4.7.0/css/font-awesome.min.css" rel="stylesheet">
 
     <link rel="stylesheet" href="https://2018.igem.org/Team:XMU-China/css/cover?action=raw&ctype=text/css">
 
     <link rel="stylesheet" href="https://2018.igem.org/Team:XMU-China/css/cover?action=raw&ctype=text/css">
 
     <link rel="stylesheet" href="https://2018.igem.org/Team:XMU-China/css/footer?action=raw&ctype=text/css">
 
     <link rel="stylesheet" href="https://2018.igem.org/Team:XMU-China/css/footer?action=raw&ctype=text/css">
 
     <link rel="stylesheet" href="https://2018.igem.org/Team:XMU-China/css/nav?action=raw&ctype=text/css">
 
     <link rel="stylesheet" href="https://2018.igem.org/Team:XMU-China/css/nav?action=raw&ctype=text/css">
     <link rel="stylesheet" href="https://2018.igem.org/Team:XMU-China/css/nav_mobile?action=raw&ctype=text/css">
+
     <link rel="stylesheet" href="https://2018.igem.org/Team:XMU-China/css/interlab?action=raw&ctype=text/css">
    <link rel="stylesheet" href="https://2018.igem.org/Team:XMU-China/css/desciption?action=raw&ctype=text/css">
+
 
     <link rel="stylesheet" href="https://2018.igem.org/Team:XMU-China/css/font?action=raw&ctype=text/css">
 
     <link rel="stylesheet" href="https://2018.igem.org/Team:XMU-China/css/font?action=raw&ctype=text/css">
 +
    <link rel="stylesheet" href="https://2018.igem.org/Team:XMU-China/css/nav_mobile?action=raw&ctype=text/css">
 
     <link rel="stylesheet" href="https://2018.igem.org/Team:XMU-China/css/material-scrolltop?action=raw&ctype=text/css">
 
     <link rel="stylesheet" href="https://2018.igem.org/Team:XMU-China/css/material-scrolltop?action=raw&ctype=text/css">
 
</head>
 
</head>
  
 
<body>
 
<body>
 +
    <header></header>
 
     <div id="container">
 
     <div id="container">
 
         <header>
 
         <header>
Line 57: Line 58:
 
                             <ul>
 
                             <ul>
 
                                 <li><a href="https://2018.igem.org/Team:XMU-China/Hardware">Overview</a></li>
 
                                 <li><a href="https://2018.igem.org/Team:XMU-China/Hardware">Overview</a></li>
                                 <li><a href="https://2018.igem.org/Team:XMU-China/Hardware/Microfluidic_Chips">Microfluidic chips</a></li>
+
                                 <li><a href="https://2018.igem.org/Team:XMU-China/Hardware#Microfluidic_Chips">Microfluidic chips</a></li>
                                 <li><a href="https://2018.igem.org/Team:XMU-China/Hardware/Fluorescenc_Detection">Fluorescence Detection</a></li>
+
                                 <li><a href="https://2018.igem.org/Team:XMU-China/Hardware#Fluorescence_Detection">Fluorescence Detection</a></li>
                                 <li><a href="https://2018.igem.org/Team:XMU-China/Hardware/Straberry_Pi">Straberry Pi</a></li>
+
                                 <li><a href="https://2018.igem.org/Team:XMU-China/Hardware#Raspberry_Pi">Raspberry Pi</a></li>
 +
                                <li><a href="https://2018.igem.org/Team:XMU-China/Hardware#Application">Application</a></li>
 
                                 <li><a href="https://2018.igem.org/Team:XMU-China/Applied_Design">Applied Design</a></li>
 
                                 <li><a href="https://2018.igem.org/Team:XMU-China/Applied_Design">Applied Design</a></li>
                                 <li><a href="https://2018.igem.org/Team:XMU-China/Software">APP</a></li>
+
                                 <li><a href="https://2018.igem.org/Team:XMU-China/Software">Software</a></li>
 
                             </ul>
 
                             </ul>
 
                         </li>
 
                         </li>
Line 111: Line 113:
 
             </div>
 
             </div>
 
         </header>
 
         </header>
     </div>
+
     </div> -->
 
     <script src="js/jquery-1.11.0.min.js"></script>
 
     <script src="js/jquery-1.11.0.min.js"></script>
 
     <!-- <script src="js/hc-mobile-nav.js"></script> -->
 
     <!-- <script src="js/hc-mobile-nav.js"></script> -->
Line 166: Line 168:
 
                 </div>
 
                 </div>
 
                 <div id="Hardwork">
 
                 <div id="Hardwork">
                     <div class="nav-word">Hardware</div>
+
                     <div class="nav-word">Hardwork</div>
 
                     <ul>
 
                     <ul>
 
                         <li><a href="https://2018.igem.org/Team:XMU-China/Hardware">Overview</a></li>
 
                         <li><a href="https://2018.igem.org/Team:XMU-China/Hardware">Overview</a></li>
                         <li><a href="https://2018.igem.org/Team:XMU-China/Hardware/Microfluidic_Chips">Microfluidic chips</a></li>
+
                         <li><a href="https://2018.igem.org/Team:XMU-China/Hardware#Microfluidic_Chips">Microfluidic chips</a></li>
                         <li><a href="https://2018.igem.org/Team:XMU-China/Hardware/Fluorescenc_Detection">Fluorescence Detection</a></li>
+
                         <li><a href="https://2018.igem.org/Team:XMU-China/Hardware#Fluorescence_Detection">Fluorescence Detection</a></li>
                         <li><a href="https://2018.igem.org/Team:XMU-China/Hardware/Straberry_Pi">Straberry Pi</a></li>
+
                         <li><a href="https://2018.igem.org/Team:XMU-China/Hardware#Raspberry_Pi">Raspberry Pi</a></li>
 +
                        <li><a href="https://2018.igem.org/Team:XMU-China/Hardware#Application">Application</a></li>
 
                         <li><a href="https://2018.igem.org/Team:XMU-China/Applied_Design">Applied Design</a></li>
 
                         <li><a href="https://2018.igem.org/Team:XMU-China/Applied_Design">Applied Design</a></li>
                         <li><a href="https://2018.igem.org/Team:XMU-China/Software">APP</a></li>
+
                         <li><a href="https://2018.igem.org/Team:XMU-China/Software">Software</a></li>
 
                     </ul>
 
                     </ul>
 
                 </div>
 
                 </div>
Line 191: Line 194:
 
                     </a>
 
                     </a>
 
                 </div>
 
                 </div>
             </div>
+
             </div> -->
 
         </div>
 
         </div>
 
         <div class="clear"></div>
 
         <div class="clear"></div>
 
         <div class="description_banner">
 
         <div class="description_banner">
             <div class="word">Description</div>
+
             <div class="word">Hardware</div>
 
         </div>
 
         </div>
 
         <nav class="Quick-navigation">
 
         <nav class="Quick-navigation">
 
             <div class="Quick-navigation_word">
 
             <div class="Quick-navigation_word">
                 <img  src="https://static.igem.org/mediawiki/2018/f/f5/T--XMU-China--right0.png">
+
                 <img  src="https://static.igem.org/mediawiki/2018/e/e6/T--XMU-China--right50.png">
                 <a href="#ABCDsystem" class="Quick-navigation-item">
+
                 <a href="#Overview" class="Quick-navigation-item">
                     <img id="turn_img" src="https://static.igem.org/mediawiki/2018/d/db/T--XMU-China--right1.png">
+
                     <img id="turn_img" src="https://static.igem.org/mediawiki/2018/5/50/T--XMU-China--right51.png">
                     <a href="#ABCDsystem"id="Quick_A">ABCDsystem</a></a>
+
                     <a href="#Overview"id="Quick_A">Overview</a></a>
                 <a href="#OMVs" class="Quick-navigation-item" >
+
                 <a href="#Microfluidic_Chips" class="Quick-navigation-item" >
                     <img id="turn_img" src="https://static.igem.org/mediawiki/2018/c/cd/T--XMU-China--right2.png">
+
                     <img id="turn_img" src="https://static.igem.org/mediawiki/2018/0/04/T--XMU-China--right52.png">
                     <a href="#OMVs" id="Quick_B">OMVs</a></a>
+
                     <a href="#Microfluidic_Chips" id="Quick_B">Microfluidic Chips</a></a>
                 <a href="#Supporting" class="Quick-navigation-item">
+
                 <a href="#Fluorescence_Detection" class="Quick-navigation-item">
                     <img id="turn_img" src="https://static.igem.org/mediawiki/2018/1/1c/T--XMU-China--right3.png">
+
                     <img id="turn_img" src="https://static.igem.org/mediawiki/2018/d/d0/T--XMU-China--right53.png">
                     <a href="#Supporting" id="Quick_C">Supporting</a></a>
+
                     <a href="#Fluorescence_Detection" id="Quick_C">Fluorescence Detection</a></a>
 +
                <a href="#Raspberry_Pi" class="Quick-navigation-item">
 +
                    <img id="turn_img" src="https://static.igem.org/mediawiki/2018/1/11/T--XMU-China--right54.png">
 +
                    <a href="#Raspberry_Pi"id="Quick_D">Raspberry Pi</a></a>
 +
                <a href="#Application" class="Quick-navigation-item">
 +
                    <img id="turn_img" src="https://static.igem.org/mediawiki/2018/b/ba/T--XMU-China--right55.png">
 +
                    <a href="#Application"id="Quick_F">Application</a></a>
 
             </div>
 
             </div>
 
         </nav>
 
         </nav>
         <div class="main">
+
         <div class="main Entrepreneurship">
             <section id="ABCDsystem" class="js-scroll-step">
+
             <section id="Overview" class="js-scroll-step">
 
                 <div class="headline">
 
                 <div class="headline">
                     ABCDsystem
+
                     Overview
 
                 </div>
 
                 </div>
 
                 <h1>Background</h1>
 
                 <h1>Background</h1>
                 <p>Protein plays a significant role in performing physiological functions<sup>[1]</sup>. However, in diseased cells, protein carrying out a certain function may indicate the proceedings of disease. Such protein could be sorted to biomarkers, which have been regarded as the targets of disease detection and treatment in recent years.<sup>[2]-[4]</sup> Therefore, detecting those biomarkers of protein-type becomes more and more critical to biological and medical fields.
+
                 <p>Nowadays, most disease-diagnosing methods are confined to specific delicate testing apparatus, which are expensive, time-consuming and low sensitivity. The study of <i>Point-of-care</i> testing (POCT), also called bedside testing (with the definition of medical diagnostic testing at or near the time and place of patient care), has become very heated because of its convenience, simplicity and highly efficiency. <i>Internet of things</i> (IoT) is the network of physical devices, vehicles, home appliances, and other items embedded with electronics, software, sensors, actuators, and connectivity which enables the connection and exchange of data.</p>
                </p>
+
                <p>Here we came up with a design. We combined the idea of our project <i>Aptamer-based Cell-free Detection system</i> (ABCD system), IoT, and the above concept of POCT so as to develop a microfluidic device, which is small while convenient for real-time detection of cancer. </p>
                <p>There are two main detecting approaches to detect a particular protein in a complex sample. One is direct determination of the content after purification, and the other is binding assays which include a target recognition probe and a signal transducer. The former approach includes gel filtration chromatography, ion exchange chromatography, nickel column and more. While on the down side, these methods involve high costs, strict equipment requirements and other drawbacks, which are not suitable for promotion and application. The enzyme-linked immunosorbent assay (ELISA) is a typical representative of the latter approach, nevertheless, such assays using antibodies as affinity ligands have cross-reactivity of antibodies compromising the specificity to the target of interest.<sup>[5]</sup> What’s worse, the premise of using ELISA is to find the corresponding antibodies, but the fact is that not all proteins can find their specific antibody protein. That is to say, the use of ELISA is also limited.
+
                <p>Given that the biomarkers of different cancers are overlapping and the time was limited, we just took the pancreatic cancer as an example to certify the feasibility of our testing theory as well as our device.</p>
                 </p>
+
                 <h1>Designs</h1>
                 <p>In terms of binding assays, using aptamers as affinity ligands to recognize specific proteins are better than those using antibodies. Aptamers are short, synthetic single stranded oligonucleotides (DNA or RNA) that can bind to target molecules with high affinity and specificity.<sup>[6]-[9]</sup> They are commonly selected from random sequence libraries, using the systematic evolution of ligands by exponential enrichment (SELEX) techniques.<sup>[10]</sup> Advantages of aptamers over antibodies include longer shelflife, improved thermal stability and ease of modification and conjugation.<sup>[11]</sup>
+
                 <p>We gave our testing device a name, “ <i>Eye of Agamotto</i>” (EA), whose inspiration comes from Time Stone owned by Dr.Strange(Marvel).</p>
                </p>
+
                <p>In general, EA consists of four parts, namely the Microfluidic chip, the fluorescence detection apparatus, <i>Raspberry Pi</i> (RPi) and a mobile-phone application(Software).Among these four parts, Raspberry Pi is the main operating system of the entire device, and its functions include chip-driving controlling, image capturing and server-client data transmission.</p>
                 <p>An interesting binding assay is to use aptamers as the target recognition probes and CRISPR-Cas12a (Cpf1) as the signal amplifier, which is called Aptamer Based Cell-free Detection system(ABCD system, Figure 1). We developed this system to detect those biomarkers of protein-type for the purpose of disease detection or staging.
+
                 <p>At the beginning,the sample,which is added into our designed microfluidic chip based on ABCD system, will react to Cas12a and give out the fluorescence signal. Then RPi controlled camera captures the image that would be transmitted to App through Socket. In the meantime, the App will convert the image results into visual and readable analysis reports based on its internal machine learning sample database. Finally, App would also achieve Information Sharing between User and Doctor.</p>
                </p>
+
                 <p class="F25"><img src="https://static.igem.org/mediawiki/2018/f/f4/T--XMU-China--hardware-1.png"></p>
                 <p class="F1">
+
                    <p>The overwhelming advantage of EA is that it gives the best interpretation of POCT. EA can overcome the drawback that some tumor/cancer detections could only be achieved in the big clinical laboratory by large and expensive equipment. It can be more widely used in the community hospitals,especially in remote areas which are short of necessary medical resources. In addition, EA can also be used for risk-monitoring by people who have familial-hereditary disease at their home.</p>
                    <img src="https://static.igem.org/mediawiki/2018/e/e2/T--XMU-China--ABCD_system.png">
+
                    <p class="F3"><img src="https://static.igem.org/mediawiki/2018/1/16/T--XMU-China--electronic_circui_testing2.png">
                    <p class="Figure_word">Figure 1. <strong>A</strong>ptamer <strong>B</strong>ased <strong>C</strong>ell-free <strong>D</strong>etection system.</p>
+
                        <p class="Figure_word">Figure1(UP): The Whole Design of our hardware – Eye of Agamotto</p>
                </p>
+
                    </p>
                <h1>Abstract</h1>
+
            </section>
                <p>The core of the ABCD system is the specific binding of the aptamer and its target protein. We immobilize the aptamer-“complementary strand” complex on a solid phase, using a “competitive” approach to free the “complementary strand”; then the “complementary strand” was detected using the trans-cleavage property of the Cpf1 protein, which allows the fluorescence recovery of the static quenched complex whose fluorophore and quencher are linked by a ssDNA. In summary, we initially transform the protein signal to the acid signal, then transform the nucleic acid signal to the fluorescence signal. We use aptamer SYL3C<sup>[12]</sup> against EpCAM, an epithelial cell adhesion molecule that is highly expressed on the surface of adenocarcinoma cells, to test the feasibility of our system.</p>
+
            <section id="Microfluidic_Chips" class="js-scroll-step">
                <h1 class="reference">Reference</h1>
+
                <div class="headline">
                <p>
+
                    Microfluidic chips
                    [1] Janet Iwasa, Wallace Marshall. Karp's Cell and Molecular Biology: Concepts and Experiments (8th ed.). <i>Wiley: Hoboken, NJ.</i> <strong>2016</strong>, 48-49.
+
                </div>
                    <br>[2] J. K. Aronson. Biomarkers and surrogate endpoints. <i>British Journal of Clinical Pharmacology.</i> <strong>2005</strong>, 59, 491-494.
+
                <p> According to the model of Aptamer Based Cell Free testing system(ABCD System), we put forward the following design using traditional material for hardware—PMMA as the layers.</p>
                    <br>[3] Kyle Strimbu, Jorge A. Tavel. What are biomarkers? <i>Current Opinion in HIV and AIDS.</i> <strong>2010</strong>, 5, 463–466.
+
                <p> There are two rooms and two pipelines in our microfluidic chips. The first room is Incubation Room, where we has already covered with BAS systems(Biotin-Avidin System). Inspired by the project of <a class="click_here" href="链接至https://2017.igem.org/Team:EPFL/Description/Aptamers">2017 EPFL</a>, we used <strong>ternary affinity coating(TERACOAT) method<sup>[1]</sup></strong> to pre-treat our microfluidic chip, aiming to coat the aptamers which will compete with target protein. The second room is Detection Room, and we put Cas12a (Cfp1) and DNase Alert in advance to achieve it that we convert the protein signal to fluorescence signal. What’s more, there is a pipeline we named Pneumatic Valve between Incubation Room and Detection Room. It could control liquid flow through changing the motor speed, which would generate differential air pressure caused by barometric pressure and centrifugal force.</p>
                    <br>[4] Biomarkers Definitions Working Group. Biomarkers and surrogate endpoints: Preferred definitions and conceptual framework. <i>Clin. Pharmacol. Ther.</i> <strong>2001</strong>, 69, 89-95.
+
                <p> When the samples are added into loading slot, they would flow into the first room (Incubation Room).The biomarker would compete the complementary sequences in the aptamer, which would flow to the second room(Detection Room) by increasing rotate speed. In the second room, the complementary sequence would activate the Cas12a (Cfp1) to cut DNase Alert. The short sequence between Quencher and Fluorophore is cut and then the quencher wouldn’t restrain the fluorophore anymore. Above all, it would give out the green fluorescence we want in detecting room.</p>
                    <br>[5] Hongquan Zhang, Feng Li, Brittany Dever, Xing-Fang Li, X. Chris Le. DNA-Mediated Homogeneous Binding Assays for Nucleic Acids and Proteins. <i>Chem. Rev.</i> <strong>2013</strong>, 113, 2812-2841.
+
                <p class="F3"><img src="https://static.igem.org/mediawiki/2018/6/67/T--XMU-China--hardware-2.png"><img src="https://static.igem.org/mediawiki/2018/5/52/T--XMU-China--hardware-3.png">
                    <br>[6] Larry Gold, Barry Polisky, Olke Uhlenbeck, Michael Yarus. Diversity of Oligonucleotide Functions. <i>Annu. Rev. Biochem.</i> <strong>1995</strong>, 64, 763-797.
+
                     <p class="Figure_word">Figure 2: The Microfluidic Chips Cutaway View(UP) and the Sandwich Structure of BAS(Biotin-Avidin System)(DOWN)</p>
                    <br>[7] Camille L.A. Hamula, Jeffrey W. Guthrie, Hongquan Zhang, Xing-Fang Li, X. Chris Le. Selection and analytical applications of aptamers. <i>Trends Anal. Chem.</i> <strong>2006</strong>, 25, 681-691.
+
                    <br>[8] Renee K. Mosing, Shaun D. Mendonsa, Michael T. Bowser. Capillary Electrophoresis-SELEX Selection of Aptamers with Affinity for HIV-1 Reverse Transcriptase. <i>Anal. Chem.</i> <strong>2005</strong>, 77, 6107-6112.
+
                    <br>[9] Maxim Berezovski, Andrei Drabovich, Svetlana M. Krylova, Michael Musheev, Victor Okhonin, Alexander Petrov, Sergey N. Krylov. Nonequilibrium Capillary Electrophoresis of Equilibrium Mixtures: A Universal Tool for Development of Aptamers. <i>J. Am. Chem. Soc.</i> <strong>2005</strong>, 127, 3165-3171.
+
                    <br>[10] M Darmostuk, S Rimpelova, H Gbelcova, T Ruml. Current approaches in SELEX: an update to aptamer selection technology. <i>Biotechnology Advances.</i> <strong>2015</strong>, 33, 1141-1161.
+
                     <br>[11] Sumedha D. Jayasena. Aptamers: an emerging class of molecules that rival antibodies in diagnostics. <i>Clin. Chem.</i> <strong>1999</strong>, 45, 1628-1650.
+
                    <br>[12] Yanling Song, Zhi Zhu, Yuan An, Weiting Zhang, Huimin Zhang, Dan Liu, Chundong Yu, Wei Duan, Chaoyong James Yang. Selection of DNA Aptamers against Epithelial Cell Adhesion Molecule for Cancer Cell Imaging and Circulating Tumor Cell Capture. <i>Anal Chem.</i> <strong>2013</strong>, 85, 4141-4149.
+
 
                 </p>
 
                 </p>
 +
                <h1>References</h1>
 +
                <p class="reference">[1] Piraino, Francescoet, et al, ACS nano 2016, 10, 1699-1710</p>
 
             </section>
 
             </section>
             <section id="OMVs" class="js-scroll-step">
+
             <section id="Fluorescence_Detection" class="js-scroll-step">
 
                 <div class="headline">
 
                 <div class="headline">
                     OMVs
+
                     Fluorescence detection
 
                 </div>
 
                 </div>
                <h1>Background</h1>
+
                 <p> Given that the fluorophore of the DNaseAlert (IDT) would be excited by green light with 535 nm and give out light of 595 nm, we selected the green LED lamp beads (which give out light between 515-525 nm) as light source. The camera with specific optical filter is in the same level with the light. It will get the Emission light from sample and then take a photo of the whole microfluidic chip.</p>
                 <p>Outer-membrane vesicles (OMVs) are lipid vesicles commonly produced by Gram-negative bacteria, which are filled with periplasmic content and are 20-250 nm in diameters (Figure 1). The production of OMVs allows bacteria to interact with their environment, and OMVs have been found to mediate diverse functions, including promoting pathogenesis, and enabling bacterial delivery of nucleic acids and proteins. A recent paper by Kojima R et al. 2018, demonstrated an EXOtic device that can produce exosomes with specific nucleic acids cargo (Figure 2). We were impressed by the amazing OMVs and EXOtic device and came up with an idea to design a cell-free system to enable specific siRNA to be encapsulated into OMVs for cancer treatment.
+
                 <p class="F2"><img src="https://static.igem.org/mediawiki/2018/e/e0/T--XMU-China--Fluorescence_detection.png">
                </p>
+
                     <p class="Figure_word">Figure 3(UP): The Flow Path of Fluorescence Detection</p>
                <p class="F2">
+
                    <img src="https://static.igem.org/mediawiki/2018/4/43/T--XMU-China--OMVs11.png">
+
                    <p class="Figure_word">Figure 2. The cell envelope of Gram-negative bacteria consists of two membranes, the outer membrane and the cytoplasmic membrane. Envelope stability comes from various crosslinks including the non-covalent interactions between the PG and the porin outer-membrane protein A (OmpA).</p>
+
                </p>
+
                 <p class="F2">
+
                    <img src="https://static.igem.org/mediawiki/2018/c/c0/T--XMU-China--OMVs12.png">
+
                     <p class="Figure_word">Figure 3. Schematic illustration of the EXOtic devices. Exosomes are nanoscale extracellular lipid bilayer vesicles of endocytic origin, and they are secreted by nearly all cell types in physiological and pathological conditions. Exosomes containing the RNA packaging device (CD63-L7Ae) and mRNA (e.g., nluc-C/Dbox) can efficiently deliver specific nucleic acids.</p>
+
                </p>
+
                <h1>Abstract</h1>
+
                <p>Not only eukaryotes but also prokaryotes can produce nanoscale bubbles to fulfill diverse functions, such as cellular communication, surface modifications and the elimination of undesired components. Additionally, because of this functional versatility, OMVs have been explored as a platform for bioengineering applications. This year, we XMU-China decide to utilize OMVs as a cell-free platform to deliver our nucleic acids agents to facilitate therapeutic targeting of oncogenic KRAS in pancreatic cancer.</p>
+
                <p class="F3">
+
                    <img src="https://static.igem.org/mediawiki/2018/9/9d/T--XMU-China--OMVs13.png">
+
                    <p class="Figure_word">Figure 4. We utilize a split protein SpyTag/SpyCatcher (ST/SC) bioconjugation system to create a synthetic linkage between protein OmpA and archaeal ribosomal protein L7Ae. We fuse SpyTag with OmpA at its C-termini and N-termini respectively.</p>
+
                </p>
+
                <p class="F3">
+
                    <img src="https://static.igem.org/mediawiki/2018/d/da/T--XMU-China--OMVs14.png">
+
                    <p class="Figure_word">Figure 5. After the induction of IPTG and Arabinose, we can get L7Ae-SpyCatcher and siRNA-C/Dbox. Archaeal ribosomal protein L7Ae owns the ability to bind with C/Dbox RNA structure.</p>
+
                </p>
+
                <p class="F4">
+
                    <img src="https://static.igem.org/mediawiki/2018/9/97/T--XMU-China--OMVs15.png">
+
                    <p class="Figure_word">Figure 6. With the interaction between SpyTag and SpyCatcher, and the ability of L7Ae to be bind with C/Dbox, we can produce customizable and cell-free OMVs containing specific siRNA to traget for oncogenic gene.</p>
+
                </p>
+
                <h1 class="reference">Reference</h1>
+
                <p>
+
                    [1] Kojima R, Bojar D, Rizzi G, et al. Designer exosomes produced by implanted cells intracerebrally deliver therapeutic cargo for Parkinson’s disease treatment[J]. <i>Nature Communications.</i> <strong>2018</strong>, 9(1):1305. <br>
+
                    [2] Alves N J, Turner K B, Medintz I L, et al. Protecting enzymatic function through directed packaging into bacterial outer membrane vesicles: [J]. <i>Scientific Reports</i>, <strong>2016</strong>, 6:24866. <br>
+
                    [3] Schwechheimer C, Kuehn M J. Outer-membrane vesicles from Gram-negative bacteria: biogenesis and functions. [J]. <i>Nature Reviews Microbiology</i>, <strong>2015</strong>, 13(10):605-19. <br>
+
                    [4] Vanaja S K, Russo A J, Behl B, et al. Bacterial Outer Membrane Vesicles Mediate Cytosolic Localization of LPS and Caspase-11 Activation. [J]. <i>Cell</i>, <strong>2016</strong>, 165(5):1106-1119. <br>
+
                    [5] Kamerkar S, Lebleu V S, Sugimoto H, et al. Exosomes facilitate therapeutic targeting of oncogenic KRAS in pancreatic cancer[J]. <i>Nature</i>, <strong>2017</strong>, 546(7659):498-503. <br>
+
                    [6] https://en.wikipedia.org/wiki/Pancreatic_cancer<br>
+
 
                 </p>
 
                 </p>
 +
                <p> As shown in the figure below, this is the picture of the results we have photographed. Our No. 1 and No. 3 wells coated with EpCAM showed significant green fluorescence compared to other wells coated with random sequences. This proves that our experimental method of converting protein signals into fluorescent signals is feasible.</p>
 +
                <p class="F25"><img src="https://static.igem.org/mediawiki/2018/6/62/T--XMU-China--hardware-4.png"></p>
 
             </section>
 
             </section>
             <section id="Supporting" class="js-scroll-step">
+
             <section id="Raspberry_Pi" class="js-scroll-step">
 
                 <div class="headline">
 
                 <div class="headline">
                     Supporting
+
                     Raspberry Pi
 
                 </div>
 
                 </div>
                <h1>Background</h1>
+
                 <p> The Raspberry Pi (RPi) plays an important role as server, which can receive the command from the APP and apply it to the peripherals (motor and camera). To achieve it, all you need is just clicking the button on the mobile phone. </p>
                 <p>Tardigrades are able to tolerate almost complete dehydration by reversibly switching to an ametabolic state. This ability is called anhydrobiosis.<sup>[1]</sup>Tardigrade-specific intrinsically disordered proteins (TDPs) are essential for desiccation olerance.<sup>[2]</sup>2012, Takekazu Kunieda and his team identified five abundant heat-soluble proteins in the tardigrades, which can prevent protein-aggregation in dehydrated conditions in other anhydrobiotic organisms.<sup>[1]</sup>
+
                 <p class="F3"><img src="https://static.igem.org/mediawiki/2018/6/6f/T--XMU-China--Raspberry_Pi.png">
                </p>
+
                     <p class="Figure_word">Figure 4(UP): Circuit Diagram of Raspberry Pi Operating System</p>
                <p class="F4">
+
                    <img src="https://static.igem.org/mediawiki/2018/2/2d/T--XMU-China--TDP1.png">
+
                    <p class="Figure_word">Figure 7. Stage Photo of Tardigrades in Ant-Man 2.</p>
+
                </p>
+
                <p>In 2017, Thomas C. Boothby and his team segregated three TDP proteins in the water bears and explored their mechanism of action<sup>[3]</sup>. This is a schematic diagram of the mechanism they have done so far. At the same time, one of the 2017 iGEM teams <a href="https://2017.igem.org/Team:TUDelft/Design"><span class="click_here">TUDelft</span></a>, attempted to preserve the Cas13a protein using the TDP proteins, and they also tried to preserve the bacteria with the TDP proteins and obtained amazing outcome.
+
                    In our project, we are going to use TDPs to help preserve the protein Cas12a and OMVs.
+
                </p>
+
                <h1>Abstract</h1>
+
                <p>We have carried out research on TDP proteins this year. On the one hand, we plan to preserve the Cas12a required for protein detection and OMVs required for treatment with TDPs. On the other hand, as the wiki says, TDP is a new biological activity protector with great potential. So we are going to use TDP proteins to simplify existing methods of preserving proteins and bacteria.
+
                    There are two novel protein families with distinct subcellular localizations named Cytoplasmic Abundant Heat Soluble (CAHS) and Secretory Abundant Heat Soluble (SAHS) protein families, according to their localization. In our project, SAHS1 was used to preserve the proteins and CAHS1 was used for the preservation of the bacteria.
+
                </p>
+
                 <p class="F4">
+
                    <img src="https://static.igem.org/mediawiki/2018/a/aa/T--XMU-China--TDP2.png">
+
                     <p class="Figure_word">Figure 8. The Expression of TDPs When The Tardigrades Suffer Form Fast Drying and Slow Drying.(Thomas C. Boothby et al. 2017).</p>
+
                </p>
+
                <h1>Reference</h1>
+
                <p class="reference">
+
                    [1]. Yamaguchi A. Two Novel Heat-Soluble Protein Families Abundantly Expressed in an Anhydrobiotic Tardigrade. <i>PLoS ONE</i>, <strong>2012</strong>;7(8):e44209. <br>
+
[2]. Boothby TC. Tardigrades Use Intrinsically Disordered Proteins to Survive Desiccation. <i>Mol Cell</i>. <strong>2017</strong> Mar16;65(6):975-984.e5.
+
 
+
 
                 </p>
 
                 </p>
 +
                <p>Besides, it’s worth mentioning that it can execute the whole series detection processes automatically. We used SSH to make a connection between RPi and IP address, and programmed in RPi. We called Picamera Function by Python to achieve imaging-capture, and called Wringpi by C-language. We made Speed-controlling come to realize by PID speed mode.</p>
 +
                <p class="F3"><img src="https://static.igem.org/mediawiki/2018/9/9e/T--XMU-China--circuit2.png"></p>
 +
                    <p> The speed acquisition is realized by the encoder and the call interrupt-function. The RPi detects the waveform (square wave) returned by the encoder through the pin. It generates an external trigger when electrical level changes, and then it enters the interrupt function so as to realize counting and come to null. It could convert to the current motor’s speed by a pulse count for a fixed time. The maximum output voltage of PWM is only 3.3V.But the voltage will be applied to the signal input through 12V battery resistance transformer mode, which can realize 12V~0V voltage regulation, that is, speed regulation in the range of 500~0rpm. NodeJS calls the corresponding file and executes the corresponding program by receiving signals and parameters, which makes RPi’s corresponding to mobile phone’s command be realized. More details about the principle of the Raspberry Pi,please switch to our code on the Github(链接待给).</p>
 +
            </section>
 +
            <section id="Application" class="js-scroll-step">
 +
                <div class="headline ">
 +
                    Application
 +
                </div>
 +
                <p> In order to conveniently control our hardware for users, we have designed our own App which can be used with EA. It is worth mentioning that our App gathers AIT (Artificial Intelligence Technology) and blocks chain technology, equipped with functions providing excellent user experience. According to the navigation bar, we can easily find that App consists of four function modules: Control, Analysis, Interaction and Info.</p>
 +
                <p class="F2"><img src="https://static.igem.org/mediawiki/2018/e/e5/T--XMU-China--hardware-5.png"></p>
 +
                    <p> The first function module named Control, which is used to control the operation of EA. There is a switch which can control the power-driven machine to turn on or off . And the PHOTO button can be used to control the camera to capture the fluorescent signal,and display it on the mobile phone. In addition, users are free to control the speed of the revolution(Auto/Seton). What’s more, users can press the SET button to change the speed and the REQUIRE button to require the current speed.</p>
 +
                    <p> The second function module named Analysis aims at taking advantage of AIT to analyze the images that EA has already photographed. The technology we chose is Tensorflow-the second generationartificial intelligent learning system developed by Google based on DistBelief. When an user takes a photo, the photo will be sent to our cloud server. In the cloud server, there are some modules which have been trained by large amounts of samples with CNN (Convolutional Neural Network). Intelligently, the photo uploaded will match the model by machine learning and user can obtain the information containing analysis results accurately and efficiently from App.</p>
 +
                    <p> The third function module named Interaction. It is based on block chain technology. In our cloud server, we have already established a private chain of Ethereum, and we will issue our own digital currency provided for users to deploy smart contract of their own, including all theirdiagnostic messages. There is a One-to-One correspondence between a user and a doctor. When a smart contract is deployed, it allows only one doctor to confirm. Later the doctor can write the therapeutic methods or suggestions into the smart contract to which the patient can refer. On account of its transparency, openness and immutable property, a medical certificate (smart contract) can be corresponded to one specific patient and one specific doctor. Thus, it can effectively avoid medical dispute such as misdiagnose and unscrupulous disavowing.</p>
 +
                    <p> The last function module named Info.contains introduction of our teamand some users’ information.</p>
 +
                    <p> Following the function recommended above comes the introduction about the communication mechanism of our App. It is based on three-party communication among Raspberry Pi, App, and cloud server. The instruction sent from App will first arrive cloud server,and will be transmit to Raspberry Pi by server. Actually, the instruction sent from Raspberry will be in a similar way. What’s more, the machine learning and mining mechanism of block chain will be operating in the cloud server, thus we can enhance operational efficiency and real-time performance.</p>
 
             </section>
 
             </section>
 
         </div>
 
         </div>

Revision as of 08:02, 16 October 2018

Team:XMU-China/Hardware - 2018.igem.org

-->
Hardware
Overview

Background

Nowadays, most disease-diagnosing methods are confined to specific delicate testing apparatus, which are expensive, time-consuming and low sensitivity. The study of Point-of-care testing (POCT), also called bedside testing (with the definition of medical diagnostic testing at or near the time and place of patient care), has become very heated because of its convenience, simplicity and highly efficiency. Internet of things (IoT) is the network of physical devices, vehicles, home appliances, and other items embedded with electronics, software, sensors, actuators, and connectivity which enables the connection and exchange of data.

Here we came up with a design. We combined the idea of our project Aptamer-based Cell-free Detection system (ABCD system), IoT, and the above concept of POCT so as to develop a microfluidic device, which is small while convenient for real-time detection of cancer.

Given that the biomarkers of different cancers are overlapping and the time was limited, we just took the pancreatic cancer as an example to certify the feasibility of our testing theory as well as our device.

Designs

We gave our testing device a name, “ Eye of Agamotto” (EA), whose inspiration comes from Time Stone owned by Dr.Strange(Marvel).

In general, EA consists of four parts, namely the Microfluidic chip, the fluorescence detection apparatus, Raspberry Pi (RPi) and a mobile-phone application(Software).Among these four parts, Raspberry Pi is the main operating system of the entire device, and its functions include chip-driving controlling, image capturing and server-client data transmission.

At the beginning,the sample,which is added into our designed microfluidic chip based on ABCD system, will react to Cas12a and give out the fluorescence signal. Then RPi controlled camera captures the image that would be transmitted to App through Socket. In the meantime, the App will convert the image results into visual and readable analysis reports based on its internal machine learning sample database. Finally, App would also achieve Information Sharing between User and Doctor.

The overwhelming advantage of EA is that it gives the best interpretation of POCT. EA can overcome the drawback that some tumor/cancer detections could only be achieved in the big clinical laboratory by large and expensive equipment. It can be more widely used in the community hospitals,especially in remote areas which are short of necessary medical resources. In addition, EA can also be used for risk-monitoring by people who have familial-hereditary disease at their home.

Figure1(UP): The Whole Design of our hardware – Eye of Agamotto

Microfluidic chips

According to the model of Aptamer Based Cell Free testing system(ABCD System), we put forward the following design using traditional material for hardware—PMMA as the layers.

There are two rooms and two pipelines in our microfluidic chips. The first room is Incubation Room, where we has already covered with BAS systems(Biotin-Avidin System). Inspired by the project of 2017 EPFL, we used ternary affinity coating(TERACOAT) method[1] to pre-treat our microfluidic chip, aiming to coat the aptamers which will compete with target protein. The second room is Detection Room, and we put Cas12a (Cfp1) and DNase Alert in advance to achieve it that we convert the protein signal to fluorescence signal. What’s more, there is a pipeline we named Pneumatic Valve between Incubation Room and Detection Room. It could control liquid flow through changing the motor speed, which would generate differential air pressure caused by barometric pressure and centrifugal force.

When the samples are added into loading slot, they would flow into the first room (Incubation Room).The biomarker would compete the complementary sequences in the aptamer, which would flow to the second room(Detection Room) by increasing rotate speed. In the second room, the complementary sequence would activate the Cas12a (Cfp1) to cut DNase Alert. The short sequence between Quencher and Fluorophore is cut and then the quencher wouldn’t restrain the fluorophore anymore. Above all, it would give out the green fluorescence we want in detecting room.

Figure 2: The Microfluidic Chips Cutaway View(UP) and the Sandwich Structure of BAS(Biotin-Avidin System)(DOWN)

References

[1] Piraino, Francescoet, et al, ACS nano 2016, 10, 1699-1710

Fluorescence detection

Given that the fluorophore of the DNaseAlert (IDT) would be excited by green light with 535 nm and give out light of 595 nm, we selected the green LED lamp beads (which give out light between 515-525 nm) as light source. The camera with specific optical filter is in the same level with the light. It will get the Emission light from sample and then take a photo of the whole microfluidic chip.

Figure 3(UP): The Flow Path of Fluorescence Detection

As shown in the figure below, this is the picture of the results we have photographed. Our No. 1 and No. 3 wells coated with EpCAM showed significant green fluorescence compared to other wells coated with random sequences. This proves that our experimental method of converting protein signals into fluorescent signals is feasible.

Raspberry Pi

The Raspberry Pi (RPi) plays an important role as server, which can receive the command from the APP and apply it to the peripherals (motor and camera). To achieve it, all you need is just clicking the button on the mobile phone.

Figure 4(UP): Circuit Diagram of Raspberry Pi Operating System

Besides, it’s worth mentioning that it can execute the whole series detection processes automatically. We used SSH to make a connection between RPi and IP address, and programmed in RPi. We called Picamera Function by Python to achieve imaging-capture, and called Wringpi by C-language. We made Speed-controlling come to realize by PID speed mode.

The speed acquisition is realized by the encoder and the call interrupt-function. The RPi detects the waveform (square wave) returned by the encoder through the pin. It generates an external trigger when electrical level changes, and then it enters the interrupt function so as to realize counting and come to null. It could convert to the current motor’s speed by a pulse count for a fixed time. The maximum output voltage of PWM is only 3.3V.But the voltage will be applied to the signal input through 12V battery resistance transformer mode, which can realize 12V~0V voltage regulation, that is, speed regulation in the range of 500~0rpm. NodeJS calls the corresponding file and executes the corresponding program by receiving signals and parameters, which makes RPi’s corresponding to mobile phone’s command be realized. More details about the principle of the Raspberry Pi,please switch to our code on the Github(链接待给).

Application

In order to conveniently control our hardware for users, we have designed our own App which can be used with EA. It is worth mentioning that our App gathers AIT (Artificial Intelligence Technology) and blocks chain technology, equipped with functions providing excellent user experience. According to the navigation bar, we can easily find that App consists of four function modules: Control, Analysis, Interaction and Info.

The first function module named Control, which is used to control the operation of EA. There is a switch which can control the power-driven machine to turn on or off . And the PHOTO button can be used to control the camera to capture the fluorescent signal,and display it on the mobile phone. In addition, users are free to control the speed of the revolution(Auto/Seton). What’s more, users can press the SET button to change the speed and the REQUIRE button to require the current speed.

The second function module named Analysis aims at taking advantage of AIT to analyze the images that EA has already photographed. The technology we chose is Tensorflow-the second generationartificial intelligent learning system developed by Google based on DistBelief. When an user takes a photo, the photo will be sent to our cloud server. In the cloud server, there are some modules which have been trained by large amounts of samples with CNN (Convolutional Neural Network). Intelligently, the photo uploaded will match the model by machine learning and user can obtain the information containing analysis results accurately and efficiently from App.

The third function module named Interaction. It is based on block chain technology. In our cloud server, we have already established a private chain of Ethereum, and we will issue our own digital currency provided for users to deploy smart contract of their own, including all theirdiagnostic messages. There is a One-to-One correspondence between a user and a doctor. When a smart contract is deployed, it allows only one doctor to confirm. Later the doctor can write the therapeutic methods or suggestions into the smart contract to which the patient can refer. On account of its transparency, openness and immutable property, a medical certificate (smart contract) can be corresponded to one specific patient and one specific doctor. Thus, it can effectively avoid medical dispute such as misdiagnose and unscrupulous disavowing.

The last function module named Info.contains introduction of our teamand some users’ information.

Following the function recommended above comes the introduction about the communication mechanism of our App. It is based on three-party communication among Raspberry Pi, App, and cloud server. The instruction sent from App will first arrive cloud server,and will be transmit to Raspberry Pi by server. Actually, the instruction sent from Raspberry will be in a similar way. What’s more, the machine learning and mining mechanism of block chain will be operating in the cloud server, thus we can enhance operational efficiency and real-time performance.