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<div class="navbar-linkContainer" id="linkContainer_Project"> | <div class="navbar-linkContainer" id="linkContainer_Project"> | ||
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<div class="navbar-linkContainerChild" id="linkContainer_ProjectChild">PROJECT</div> | <div class="navbar-linkContainerChild" id="linkContainer_ProjectChild">PROJECT</div> | ||
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<li class="nav-item navbarItem"> | <li class="nav-item navbarItem"> | ||
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<a href="#page-top" class="navbarItemContent">Human Practices</a> | <a href="#page-top" class="navbarItemContent">Human Practices</a> | ||
+ | <div class="collapse collapsedMenu" id="collapseHPSqz"> | ||
+ | <div class="containerCollapse"> </div> | ||
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<a href="#page-top" class="navbarItemContent">Modeling</a> | <a href="#page-top" class="navbarItemContent">Modeling</a> | ||
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<ul> | <ul> | ||
<li><a href="#project" class="active"><span class="label">Project</span></a></li> | <li><a href="#project" class="active"><span class="label">Project</span></a></li> | ||
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Revision as of 14:53, 25 September 2018
E-Coding
Storing the world one base at a time
The research for storing vast amounts of information in smaller devices has been an attention seeking topic in multidisciplinary areas of knowledge all around the world.
Baum, 1995
DNA is an attractive target for information storage because of its capacity for high-density information encoding, longevity under easily achieved conditions, and proven track record as an information bearer
Baum, 1995
Nevertheless, this potential has been limited due to the lack of efficient editing tools. CRISPR-Cas has become popular as an editing tool for its high specificity, low cost, and easy handling, compared to other editing techniques. In our work, we use Cas1-Cas2, proteins in charge of new protospacer adquisition in the CRISPR array. Predesigned sequences (-70pb aprox) in the form of ssDNA are produced in E.coli by induction of a promoter, and adquired by the complex Cas1-Cas2 to be integrated into the array. To produce this oligonucleotides, we use the retrotranscriptase EC86. A subsequent sequencing of the array will confirm the integration of the oligos in the CRISPR locus. We measure the integration rate in terms of stimuli intensity, and time. We hypothise that this system can store ordered data in vivo of many stimuli, just by changing the promoter.
Human Practices
Pollutants in Chiapas and Mexico
Our project has many applications, but we decided to face a critical environmental problem in one southern state of Mexico: Chiapas. Chiapas is a beautiful state with megadiverse ecosystems, but it also has a severe water pollution problem that affects many communities close to the natural and polluted water sources. With the help of Cecropia and CONANP we will obtain water samples from the polluted sources and analyze them with several techniques in order to make a valuable overview.