Difference between revisions of "Team:FSU/Design"

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The general structure of the MscS channel consists of seven subunits: three transmembrane helices, a C-terminus facing the cytosolic domain and an N-terminus facing the periplasmic domain. Transmembrane 1 (TM1) and TM2 form a flexible paddle for tension-sensing, while TM3 forms a linked helical pore structure. A force-activated gate exists towards the conserved cytosolic domain, which shows selectivity and stability. A channel pore is towards the N-terminus, and a selectivity filter exists in the middle of the channel. The pore has a diameter for conductance values ranging from 14-16 amps.
 
The general structure of the MscS channel consists of seven subunits: three transmembrane helices, a C-terminus facing the cytosolic domain and an N-terminus facing the periplasmic domain. Transmembrane 1 (TM1) and TM2 form a flexible paddle for tension-sensing, while TM3 forms a linked helical pore structure. A force-activated gate exists towards the conserved cytosolic domain, which shows selectivity and stability. A channel pore is towards the N-terminus, and a selectivity filter exists in the middle of the channel. The pore has a diameter for conductance values ranging from 14-16 amps.
 
<li> Our Sound-Induced Systems
 
<li> Our Sound-Induced Systems
 +
Two types of systems were tested in our experiments. The first type of system utilized ions as ligands in which their signaling was activated by sound; and the second system involved a membrane stress response, in which the cell contains pre-existing protein systems that respond to external stress on the outer membrane. In this case, the stress is sound. For our first system, we based our ion selectivity on Bacteria are generally non-selective in their transmission of ion signaling molecules
 
<li>Discussion of the design iterations your team went through</li>
 
<li>Discussion of the design iterations your team went through</li>
 
<li>Experimental plan to test your designs</li>
 
<li>Experimental plan to test your designs</li>

Revision as of 17:19, 14 September 2018

Untitled-1
DRAFT!!!!!!!!!!!!!!!!!

OVERVIEW

Our first system involves using sound as a mechanical force to open a mechanosensitive channel within the E. Coli membrane. This opening allows the transmission of our zinc ion signal to flow into the cell, activating our genetic response system. Particularly, zinc will enter the cytosol and bind to ZntR, a transcriptional activator protein for the gene zntA, which encodes a zinc exporter protein channel, ZntA.

The second system involves a protein-based stress response to sound. The protein BamE is responsible for outer membrane protein assembly, and is shown to be activated by RpoE, the sigma 24 factor of RNA polymerase, as RNA polymerase binds to the bamE promoter for the gene's transcription. RpoE is known for its response to stress that affects outer membrane proteins and membranous lipopolysaccharides.

The Rcs "Regulator Capsule Synthesis" signal transduction system is a two-component stress response that maintains the outer surface of the E. Coli cell. Proteins RscC and RcsD are inner membrane proteins that direct a signal to RcsB, a transcription factor that activates a number of genes that synthesize membrane proteins and capsules. More specifically, RcsC is a sensory histidine kinase that autophosphorylates in response to an environmental signal, and then transfers the phosphate group to RcsD, the response regulator, and then to RcsB.

The Psp "Phage Shock Protein" system involves an inner membrane protein pspA, which responds to membrane stresses and regulates the pspABCDE operon. The pspA protein suppresses the proton motive foce from extruding hydrogen protons through a damaged/leaky cell membrane due to cellular stress, and also have a likely role in protein export when conditions arise that block such activity.

What should this page contain?

  • Explanation of the engineering principles your team used in your design
  • reason sound will work, why we picked our system/ions, how the mechanosensitive channels function
  • Sound as Stress The plasma membrane is the platform for conversion of environmental stimuli into biochemical signals that induce a genetic response within the cell. While there are few studies that focus on sound as an environmental stimulus on bacteria, there is a plethora of evidence for similar stimuli, such as osmotic shock, heat shock, and metal ion exposure. We hypothesize that sound may induce a similar "shock" response on the membrane. Osmotic shock, for example, can create turgor pressure upon the plasma membrane when extracellular solute concentration is low, we hypothesize that sound can cause a similar pressure on the plasma membrane, thus resulting in stress.
  • Mechanosensitive Channels for Transduction of Sound Since sound is ultimately a wave of pressure, it can be considered to be a mechanical stress. Within the plasma membrane of E. Coli cells exist various mechanosensitive protein channels, whose primary role is to protect the cell integrity from osmolarity transition. The most common "Msc" channels in E. Coli are MscM (mini-conductance), MscS (small conductance), and MscL (large conductance). They respond to mechanical stimuli by transmitting ions and electric flux via a gate-opening mechanism, changing the cell's membrane potential. Mechanical stimuli include changes in the tension of the lipid bilayer of the plasma membrane, created by a deformation of the lipid membrane that affects the membrane curvature and induces a bilayer-protein hydrophobic mismatch. We hypothesize that sound exertion can create such a tension, forcing the channel from a closed state to an open state. flex The general structure of the MscS channel consists of seven subunits: three transmembrane helices, a C-terminus facing the cytosolic domain and an N-terminus facing the periplasmic domain. Transmembrane 1 (TM1) and TM2 form a flexible paddle for tension-sensing, while TM3 forms a linked helical pore structure. A force-activated gate exists towards the conserved cytosolic domain, which shows selectivity and stability. A channel pore is towards the N-terminus, and a selectivity filter exists in the middle of the channel. The pore has a diameter for conductance values ranging from 14-16 amps.
  • Our Sound-Induced Systems Two types of systems were tested in our experiments. The first type of system utilized ions as ligands in which their signaling was activated by sound; and the second system involved a membrane stress response, in which the cell contains pre-existing protein systems that respond to external stress on the outer membrane. In this case, the stress is sound. For our first system, we based our ion selectivity on Bacteria are generally non-selective in their transmission of ion signaling molecules
  • Discussion of the design iterations your team went through
  • Experimental plan to test your designs
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