Difference between revisions of "Team:IIT Delhi/Photobleaching"

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                                                         <button class="dropbtn2"><a href="https://2017.igem.org/Team:IIT_Delhi">iGEM IIT Delhi</a></button>
 
                                                         <button class="dropbtn2"><a href="https://2017.igem.org/Team:IIT_Delhi">iGEM IIT Delhi</a></button>
<div class = "right_menu">
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        <div class = "right_menu">
 
   <div class="dropdown">
 
   <div class="dropdown">
 
     <button class="dropbtn">Project  
 
     <button class="dropbtn">Project  
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<br>
  
 
<!-- Banner -->
 
<!-- Banner -->
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</section>
 
</section>
  
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             <h2 class="h2font">LAB PROTOCOLS</h2>
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             <h2 class="h2font">Deterministic Model</h2>
  
 
             <p> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
 
             <p> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
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&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
 
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
 
  </p>
 
  </p>
<h2 id="pfont">Accurate Experimenting for Accurate Results !!</h2>
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<h2 id="pfont" style = "text-align : left; ">
          </header>
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<left>The biological networks are highly nonlinear and exhibit interesting phenotypical behaviour for certain operating conditions. One of such behaviour is the limit cycle in the
          <button class="accordion back1" style="font-weight: bold;">Transformation</button>
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          <div class="panel paddingright">
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+
<!--<u><b><h4 id="pfont"  style="font-size: 90%;">Preparation of competent  cells:-</h4></b></u>-->
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<b id="pfont">Preparation of competent  cells:-</b>
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<div align="left" style="font-size: 84%;">
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<ol ><left>
+
<li>Dilute an overnight culture of E. coli 1:200 with LB broth.
+
<li>Incubate at 37°C with shaking (at 200 rpm) until the cells reach early log phase (OD600 = 0.25-0.4).
+
<li>We already have 1X TSS in 4 deg fridge(old). Use it without dilution or thawing. Keep it inside the icebox just after taking out from the fridge. <br>
+
OR <br>
+
(if the above 1X TSS is not available)<br>
+
While cells are growing, thaw 2X TSS on ice and dilute an appropriate amount 1:1 with sterile distilled water (100µl of diluted TSS will be needed for each ml of cells). Chill on ice.
+
<li>  Place 2-ml aliquots of early log-phase cells into sterile 2-ml micro-centrifuge tubes and pellet the cells by centrifugation at 4°C  at 3000g for 10 min.(6-8 mins for taking part from Igem kit)
+
<li> Remove the supernatant and discard. Add 0.2 ml of the ice-cold 1X TSS and place the tubes on ice.
+
<li>Gently suspend the cells by pipetting.
+
<li> Proceed with the transformation protocol below (Step 2), or immediately freeze cells by immersion in liquid nitrogen or a dry ice/ethanol bath. Store the frozen cells at –70°C.
+
</left>
+
</ol>
+
</div>
+
  
<b id="pfont">Transformation:-</b>
+
mathematical sense, which shows a sustained oscillations of protein levels in the cell. It
<br>
+
<div align="left" style="font-size: 84%;">
+
<ol ><left>
+
<li>Thaw frozen TSS-competent cells slowly on ice(if stored at -70°C).
+
<li>Add 100 pg -200 ng (2.5 to 4 ul)(15ul for ligation product)of DNA to each tube of competent cells. <br>Note:Addition of more than 10ng of DNA may significantly decrease transformation efficiencies.
+
<li>Flick the tubes to mix the cells and DNA and incubate the cells on ice for 30 minutes. <br>
+
  
<li>  Transfer the tubes to water bath/dry bath(42°C) for 90 seconds.  
+
is quite interesting as well important to look for topologies which can produce such oscillations for different amplitude, oscillation and shape. Here, we have used a theoretical framework to begin with, for identifying topology based on following theorem.<br/><br>
<li> Transfer the tubes to ice and incubate for an additional 10 minutes.  
+
Theorem:1 (Hasting et. al.) Consider a system  ̇x = f(x), which is of ring in nature, and f is a monotone
<li>Add 800 ul (total 1 mL)of LB broth and incubate the cells at 37°C for up to 1 hour with shaking (at 200 rpm).
+
function and in the form<br/><br>
 +
<img src = "https://static.igem.org/mediawiki/2017/a/ad/T--IIT_Delhi--Deterform_1.jpg" style='border:3px solid #000000' width = "95%"><br><br>
  
<li> Centrifuge the cells at 3000g for  ~ 6min (10 mins after ligation)at 4deg(in temperature control centrifuge).
+
Then, if the Jacobian of f and x has no repeated eigenvalues and has any eigenvalue
  <li> Aspirate the tubes to leave the pellets with 1/4 broth .(keep ~300ul)
+
with positive real parts, then the system must have a consistent periodic orbit.<br/><br>
    <li>Plate the cells on-to the appropriate selective or differential medium and incubate overnight at 37°C.Check the procedure for antibiotic.
+
To design a squarewave oscillator, we used the theorem to idenify the biological system
      <ol> <li>For Ampicillin: 12ul Amp + 188 ul MQ. In MCT spread it on the culture plate before adding the DNA.
+
which can satisfy such condition. One of classical example is Repressillator (Elowitz et
        <li>For Chloramphenicol: 1:1000 volume ratio of antibiotic : culture broth. Directly suspend into the culture broth and spread it on the plate.
+
al) or 5n1 ring oscillator (Murray et al). This kind of oscillator is based on negative
          <li> For Kanamycin: 1:1000 volume ratio of antibiotic : culture broth. Directly suspend into the culture broth and spread it on the plate.
+
feedback with delay and able to produce stable limit cycle computationally and as well as
          </ol>
+
experimentally. However, these oscillators are more of a phaselag oscillator matching the
          <ul>
+
sinusoidal umbrella behavior. As philosophy behind our work is to design
<li>DNA should be added as soon as the last trace of ice in the tube disappears.
+
square wave, we exploit the system parameters to produce relaxation oscillations. The
<li>Incubate on ice for 30 minutes. Expect a 2-fold loss in TE for every 10 minutes you shorten this step.
+
relaxation oscillator typically works on the principle of level of concentration, where once
</ul>
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the level is reached it relaxes there for some additional time and falls back to another
</left>
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level and resides there for some till it jumps back (slowly). The time evolution of such
</ol>
+
trajectories portray a square wave-ish in state-space.<br/><br>
<br>
+
</div>
+
  
            </p>
+
The dynamical model of the five node oscillator can be written as;<br/><br>
          </div>
+
<img src = "https://static.igem.org/mediawiki/2017/3/38/T--IIT_Delhi--Deterform_2.jpg" style='border:3px solid #000000' width = "80%"><br><br>
  
          <button class="accordion back2" style="font-weight: bold;">Washing 96 Well Plates</button>
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where i ∈ [0 = 5, 1, 2, 3, 4, 5], xmi is the mRNA concentration level, xpi is the protein
          <div class="panel paddingleft">
+
transcription level, βm0 is the leaky expression, βmi is the production rate of mRNA, βpi
            <div align="left" style="font-size: 84%;" >
+
is the production rate of protein, γmi is the degradation/dilution of mRNA and γpi is
              <ul>
+
the degradation/dilution of protein for ith protein. The simulation results of the model
                  <li> Perform all the steps gently
+
presented in Fig. below. It is evident the such system can exhibit a oscillation resembling a
                  <li> Wash twice with tap water, jerk it off
+
squarewave.<br/><br>
                  <li> Wash twice with distilled water, jerk it off
+
<img src = "https://static.igem.org/mediawiki/2017/5/5b/T--IIT_Delhi--Fig_2_.jpg" style='border:3px solid #000000' width = "90%"><br><br>
                  <li> Put ethanol in plates and stand for 5 min
+
                  <li> Jerk it off
+
                  <li> Put open plate in oven for 20 minutes
+
                  <li> Put closed plate in UV for 10 minutes
+
              </ul>
+
<br>
+
            </div>
+
          </div>
+
  
<button class="accordion back3" style="font-weight: bold;">Agarose Gel Electrophoresis</button>
+
As the dynamical model comprises of two time-scale, one can use the singular perturbation analysis to reduce the model in to smaller one, i.e. 5th order, as discussed earlier.
          <div class="panel paddingright">
+
            <div align="left" style="font-size:84%;">
+
            <ol>           
+
              <li> <b> Prepare sufficient electrophoresis buffer (usually 1x TAE ) to fill the
+
electrophoresis tank and to cast the gel:</b><br>
+
For example, we take 2ml of TAE stock solution in an Erlenmeyer flask and make
+
the volume to 100ml by adding 98 ml of distilled water. The 1x working solution
+
is 40 mM Tris-acetate/1 mM EDTA.<br>
+
<b>It is important to use the same batch of electrophoresis buffer in both
+
the electrophoresis tank and the gel preparation.</b>
+
  
              <li>Loosely plug the neck of the Erlenmeyer flask using a paper cap. Heat the
+
The simpler version of the model, where multiple constants product are clubbed into one,
slurry in a boiling-water bath or a microwave oven until the agarose dissolves.
+
can be reproduced as follows,<br><br>
The agarose solution can boil over very easily so keep checking it. It is good to
+
<img src = "https://static.igem.org/mediawiki/2017/d/df/T--IIT_Delhi--Deterform_3.jpg" style='border:3px solid #000000' width = "70%"><br><br>
stop it after 45 seconds and give it a swirl. It can become superheated and NOT
+
boil until you take it out where upon it boils out all over your hands.
+
  
 +
where αi can be considered as the protein production rate constant and γ as the degra-
 +
dation constant. The simulation of 5th order comes model presented in FigX is almost
  
              <li>When the molten gel has cooled to ~50 deg C, add 0.5μg/ml of ethidium
+
identical to the simulation for full order model. Both of the model can exhibit sustained
bromide. Mix the gel solution thoroughly by gentle swirling.
+
square wave like response of arbitrary initial conditions.<br/></left><br>
  
              <li>While the agarose solution is cooling, choose an appropriate comb for forming
+
<img src = "https://static.igem.org/mediawiki/2017/a/af/T--IIT_Delhi--Fig_1_.jpg" style='border:3px solid #000000' width = "90%"><br><br>
the sample slots in the gel. Apply cellotape tightly onto the sodes of comb to
+
form a mold for gel.
+
  
              <li>Pour the warm agarose solution into the mold.<b>(The gel should be between
+
</h2>
3 - 5 mm thick. Check that no air bubbles are under or between the
+
          </header>
teeth of the comb).<b>
+
  
              <li>Allow the gel to set completely (30-45 minutes at room temperature), then
 
pour a small amount of electrophoresis buffer on the top of the gel, and carefully
 
remove the comb. Pour off the electrophoresis buffer. Mount the gel in the
 
electrophoresis tank. <b>Wash the Erlenmeyer flask as quick as possible. (Add
 
just enough electrophoresis buffers to cover the gel to a depth of
 
approx. 1mm).</b>
 
  
              <li>Mix the samples of DNA with 0.20 volumes of the desired 6x gel-loading dye
 
on a clean piece of cello tape spread on an even surface.
 
  
              <li>Slowly load the sample mixture into the slots of the submerged gel using a
+
         
disposable micropipette or an automatic micropipettor or a drawn-out Pasteur
+
pipette or a glass capillary tube. Load size standards into slots on both the right
+
and left sides of the gel.
+
  
              <li>Close the lid of the gel tank and attach the electrical leads so that the DNA
 
will migrate toward the positive anode (red lead). Apply a voltage of 7-10 V/cm (measured as the distance between the positive and negative electrodes). If the electrodes are 10 cm apart then run the gel at 50V. It is fine to run the gel
 
slower than this but do not run it any faster. Above 5V/cm the agarose may heat up and begin to melt with disastrous effects on your gel's resolution. If the leads have been attached correctly, bubbles should be generated at the anode and
 
cathode.
 
 
              <li>Run the gel until the loading dye has migrated an appropriate distance(~ 2/3
 
the length of gel) through the gel.
 
             
 
              <li>Remove the gel tray and place directly on a UV transilluminator or under a
 
gel doc.
 
            </ol>
 
<br><div class="paddingright paddingleft"> NOTE:
 
<ul>
 
<li>Use TBE 1x for < 1000bp(can't extract DNA) and TAE for large DNA(12-15kb)
 
<li>Percentage of agarose matters
 
<li>Gel thickness should not be more than 3-4mm.
 
<li>Comb should be cleaned well
 
<li>Add buffer before removing the comb</ul>
 
</div>
 
            </ol>
 
<br>
 
            </div>
 
          </div>
 
<button class="accordion back4" style="font-weight: bold;">Plasmid Isolation</button>
 
    <div class="panel paddingright">
 
            <div align="left" style="font-size:84%;">
 
            <ol>           
 
            <li>Inoculate 5 ml of rich medium (LB, YT, or Terrific Broth) containing the
 
appropriate antibiotic with a single colony of transformed bacteria.
 
Incubate the culture overnight at 37°C with vigorous shaking at 200
 
rpm.
 
              <li>Pour 2 ml of the culture into a microfuge tube. Centrifuge at maximum
 
speed(13400 rpm) for 4-5 minutes in a microfuge. Store the unused
 
portion(if any) of the original culture at 4°C.
 
              <li>Remove the medium by aspiration leaving the
 
bacterial pellet as dry as possible.
 
              <li>Resuspend the bacterial pellet in 100 μl of ice-cold Alkaline lysis
 
solution I by vigorous vortexing.
 
              <li>Add 200 μl of freshly prepared Alkaline lysis solution II to each
 
bacterial suspension. Close the tube tightly, and mix the contents well
 
by inverting the tube.
 
              <br>NOTE:
 
              <ol>
 
              <li>Do not vortex!
 
              <li>Do not let the reaction proceed for more than 1 minutes.
 
              </ol>
 
            <li>Add 150 μl of ice-cold Alkaline lysis solution III. Close the tube and
 
disperse Alkaline lysis solution III through the viscous bacterial lysate
 
by inverting the tube several times. Store the tube in ice for 3-5
 
minutes(optional).
 
            <li>Centrifuge the bacterial lysate for 10 minutes at maximum speed in a
 
microfuge. Collect the supernatant to a fresh 1.5 ml mctube.
 
            <li>(Optional) Add equal volume of phenol: chloroform. Mix the organic
 
and aqueous phases by vortexing and then centrifuge the emulsion at
 
maximum speed for 2 minutes in a microfuge. Transfer the aqueous
 
upper layer to a fresh tube.
 
            <li>Precipitate nucleic acids from the supernatant. Now add 2 volumes of
 
ethanol at room temperature to the supernatant in a 1.5 ml MCT. Mix
 
the solution by vortexing and then allow the mixture to stand for 2
 
minutes at room temperature(optional). Discard the pellet in the
 
original 2 ml MCT.
 
            <li>Collect the precipitated nucleic acids by centrifugation at maximum
 
speed for 10 minutes in a microfuge.
 
            <li>Discard the supernatant by aspiration. Stand the tube in an inverted
 
position on a paper towel to allow all of the fluid to drain away. Use a
 
Kim wipe or disposable pipette tip to remove any drops of fluid
 
adhering to the walls of the tube. Stand the tube for 10 minutes.
 
            <li>(Optional)Add 1 ml of 70% ethanol to the pellet and invert the closed
 
tube several times. Recover the DNA by centrifugation at maximum
 
speed for 2 minutes at in a microfuge.
 
            <li>(Optional)Remove all of the supernatant by aspiration. Take care with
 
this step, as the pellet sometimes does not adhere tightly to the tube.
 
            <li>(Optional)Remove any beads of ethanol from the tube. Store the open
 
tube at room temperature until the ethanol has evaporated and no
 
fluid is visible in the tube (5-10 minutes).
 
            <li>Store the tube for 10 minutes at 37 degrees without shaking.
 
            <li>Dissolve the nucleic acids in 20 μl of mQ ( 1/100 times the initial
 
volume in the MCT) or TE (pH 8.0) [containing 20 μg/ml Dnas e-free
 
RNase A (pancreatic RNase)] . Vortex the solution gently for a few
 
seconds and store the DNA at -20°C.
 
            </ol> 
 
<br>
 
          </div>
 
</div>
 
<button class="accordion back1" style="font-weight: bold;">Restriction Digestion</button>
 
          <div class="panel paddingright paddingleft">
 
          <div align="left" style="font-size:84%;">
 
            <ol>
 
            <li>Transfer the following solutions in a micro centrifuge tube.
 
            <li>Incubate the mixture at 37 o C for 1 h to overnight. Keep the tubes in -4o C
 
freezer or in -20o C freezer, after the incubation.
 
</ol>
 
              <br><div class="pddingleft1 paddingright">NOTE:
 
              <ul>
 
              <li>10X buffer should be added in the reaction such that its final concentration is 1x (e.g. - in
 
a 50 ul reaction 5 ul of buffer would be added).
 
              <li>Amount of DNA to be added depends on concentration and the amount of DNA to be
 
digested.
 
              <li>Make sure that the restriction enzyme does not exceed more than 10%
 
of the total reaction volume, Otherwise the glycerol and the EDTA in
 
the enzyme storage buffer may inhibit digestion process.
 
              <li>Enzymes on ice, when not in freezer
 
              <li>Mix by pipetting
 
              <li>A 50 μl reaction volume is recommended for digestion of 1 μg of substrate
 
              <li>Control DNA (DNA with multiple known sites for the enzyme, e.g. lambda or
 
adenovirus-2 DNA) with restriction enzyme to test enzyme viability
 
                <li>If the control DNA is cleaved and the experimental DNA resists cleavage, the two
 
DNAs can be mixed to determine if an inhibitor is present in the experimental
 
sample. If an inhibitor (often salt, EDTA or phenol) is present, the control DNA will
 
not cut after mixing.
 
                <li>Cleanup of the PCR fragment prior to restriction digestion is recommended. PCR
 
components can inhibit enzyme activity. In addition, the polymerase present in
 
the PCR is active during the digestion step, and can modify the newly created
 
ends by blunting them.
 
                <li>Some enzymes may bind tightly to the substrate DNA. This binding can result in
 
smearing or the presence of unexpectedly high molecular weight bands on a gel.
 
To prevent this, add SDS to a final concentration of approximately 0.1%, or use
 
Gel Loading Dye, Purple (6x), which contains sufficient SDS to dissociate the
 
enzyme from the substrate.
 
                  <li>To prevent star activity, make sure that you use the recommended buffer, that the
 
amount of glycerol in the reaction is no more than 5% of the total reaction
 
volume
 
              </ul>
 
          </div>
 
<br>
 
          </div>
 
</div>
 
<button class="accordion back2" style="font-weight: bold;" >Gel Extraction</button>
 
          <div class="panel paddingright">
 
          <div align="left" style="font-size:84%;">
 
          <ol>
 
          <li>Excise the DNA fragment from agarose gel with clean, sharp scalpel.
 
          <li>Weigh the gel slice. Add 3 volumes buffer QG to 1 volume of gel( 100 mg gel = 100 ul). ( if we
 
have 18 mg of gel take around 20 ul of buffer QG)
 
          <li>Incubate at 50 degree celsius for 10 minutes. Vortex after 5 minutes to dissolve the gel slice .
 
After gel has dissolved the color of mixture is yellow. NOTE: tilt the MCT upside down, to see if the
 
gel has completely dissolved. If it has not dissolved, incubate it for 2-3 minutes more. NOTE: if
 
mixture color is orange or violet, ad 10 ul 3M sodium acetate, pH 5.0 and mix. The mixture turns
 
yellow.
 
          <li>Add 1 gel volume isopropanol to sample and mix.
 
          <li>Take the whole volume in the MCT and transfer it to spin column.
 
          <li>Spin it on minispin for 90 sec at maximum speed.
 
          <li>Discard the flow through
 
          <li>Add 750 ul of PE buffer. in the spin column.
 
          <li>Spin it on minispin for 90 sec at maximum speed.
 
          <li>Discard the flow through and centrifuge once again for 90 seconds at maximum speed.
 
          <li>Place QIAquick column in 1.5 mL fresh MCT.
 
          <li>Add EB buffer through the QIA quick column center. ( around 20 – 25 ulL depending on
 
application)
 
          <li>Spin for 2 minutes at maximum speed in minispin.
 
          </ol>
 
<br>
 
          </div>
 
</div>
 
<button class="accordion back3" style="font-weight: bold;">Colony PCR</button>
 
          <div class="panel">
 
          <div align="centre" style="font-size:84%;">
 
          <h2 id="pfont"> Annealing Temperature 54.5 degC </h2>
 
            <table style="width:50%" class="table1">
 
  <tr>
 
    <th>Component</th>
 
    <th>Volume(uL)</th>
 
  </tr>
 
  <tr>
 
    <td>TaqMM</td>
 
    <td>10</td>
 
  </tr>
 
  <tr>
 
    <td>Forward Primer</td>
 
    <td>0.4</td>
 
  </tr>
 
  <tr>
 
<td>Reverse Primer</td>
 
    <td>0.4</td>
 
  </tr>
 
<tr>
 
<td>Colony</td>
 
    <td>Just a pinch</td>
 
  </tr>
 
<tr>
 
<td>Milli Q</td>
 
    <td>9.2</td>
 
  </tr>
 
<td>Total</td>
 
    <td>20</td>
 
</table>
 
          <br>
 
          </div>
 
</div>
 
  
 
     <br>
 
     <br>
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<table  style="font-family:'Lato'; border: 0px solid black; ">
 
<table  style="font-family:'Lato'; border: 0px solid black; ">
 
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<center> <p  style="text-align: center; color:white; font-size: 80%;">E-mail: iitd.igem@gmail.com<br>Undergraduate Laboratory<br>Department of Biotechnology and Biochemical Engineering, IIT Delhi</p></center>
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Revision as of 19:45, 1 November 2017

iGEM IIT Delhi


Deterministic Model

                                                                                                                                                                                                                 

The biological networks are highly nonlinear and exhibit interesting phenotypical behaviour for certain operating conditions. One of such behaviour is the limit cycle in the mathematical sense, which shows a sustained oscillations of protein levels in the cell. It is quite interesting as well important to look for topologies which can produce such oscillations for different amplitude, oscillation and shape. Here, we have used a theoretical framework to begin with, for identifying topology based on following theorem.

Theorem:1 (Hasting et. al.) Consider a system ̇x = f(x), which is of ring in nature, and f is a monotone function and in the form



Then, if the Jacobian of f and x has no repeated eigenvalues and has any eigenvalue with positive real parts, then the system must have a consistent periodic orbit.

To design a squarewave oscillator, we used the theorem to idenify the biological system which can satisfy such condition. One of classical example is Repressillator (Elowitz et al) or 5n1 ring oscillator (Murray et al). This kind of oscillator is based on negative feedback with delay and able to produce stable limit cycle computationally and as well as experimentally. However, these oscillators are more of a phaselag oscillator matching the sinusoidal umbrella behavior. As philosophy behind our work is to design square wave, we exploit the system parameters to produce relaxation oscillations. The relaxation oscillator typically works on the principle of level of concentration, where once the level is reached it relaxes there for some additional time and falls back to another level and resides there for some till it jumps back (slowly). The time evolution of such trajectories portray a square wave-ish in state-space.

The dynamical model of the five node oscillator can be written as;



where i ∈ [0 = 5, 1, 2, 3, 4, 5], xmi is the mRNA concentration level, xpi is the protein transcription level, βm0 is the leaky expression, βmi is the production rate of mRNA, βpi is the production rate of protein, γmi is the degradation/dilution of mRNA and γpi is the degradation/dilution of protein for ith protein. The simulation results of the model presented in Fig. below. It is evident the such system can exhibit a oscillation resembling a squarewave.



As the dynamical model comprises of two time-scale, one can use the singular perturbation analysis to reduce the model in to smaller one, i.e. 5th order, as discussed earlier. The simpler version of the model, where multiple constants product are clubbed into one, can be reproduced as follows,



where αi can be considered as the protein production rate constant and γ as the degra- dation constant. The simulation of 5th order comes model presented in FigX is almost identical to the simulation for full order model. Both of the model can exhibit sustained square wave like response of arbitrary initial conditions.






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