Line 118: | Line 118: | ||
<div class="container-fluid tsc"> | <div class="container-fluid tsc"> | ||
<div class="row"> | <div class="row"> | ||
− | <div class="col-md-4 center"><img style="width: 15vw" src="https://static.igem.org/mediawiki/2016/archive/c/c8/20161019022954%21T--Waterloo--trigger.svg" > | + | <div class="col-md-4 center"><img class="tsc1" style="width: 15vw" src="https://static.igem.org/mediawiki/2016/archive/c/c8/20161019022954%21T--Waterloo--trigger.svg" > |
− | <h4> We initiate a [PSI+] response in S. cerevisiae using a plasmid that will overexpress Sup35-NM. </h4></div> | + | <h4 id="texticles1"> We initiate a [PSI+] response in S. cerevisiae using a plasmid that will overexpress Sup35-NM. </h4></div> |
− | <div class="col-md-4 center"><img style="width: 15vw" src="https://static.igem.org/mediawiki/2016/archive/8/86/20161019023840%21T--Waterloo--signal.svg"> | + | <div class="col-md-4 center"><img class="tsc2" style="width: 15vw" src="https://static.igem.org/mediawiki/2016/archive/8/86/20161019023840%21T--Waterloo--signal.svg"> |
− | <h4> We insert a premature stop codon into an N-terminal CFP tag that will be read through and fluoresce during a [PSI+] response</h4></div> | + | <h4 id="texticles2"> We insert a premature stop codon into an N-terminal CFP tag that will be read through and fluoresce during a [PSI+] response</h4></div> |
− | <div class="col-md-4 center"><img style="width: 15vw" src="https://static.igem.org/mediawiki/2016/archive/e/e8/20161019015825%21T--Waterloo--control.svg" > | + | <div class="col-md-4 center"><img class="tsc3" style="width: 15vw" src="https://static.igem.org/mediawiki/2016/archive/e/e8/20161019015825%21T--Waterloo--control.svg" > |
− | <h4>We control read through rates by choosing the location of the premature stop codon, and can therefore control protein production in [PSI+]. We use Hsp104, a chaperone protein in S. cerevisiae, to demonstrate that our set-up phenotypically responds to the stop codon readthrough. </h4> </div> | + | <h4 id="texticles3">We control read through rates by choosing the location of the premature stop codon, and can therefore control protein production in [PSI+]. We use Hsp104, a chaperone protein in S. cerevisiae, to demonstrate that our set-up phenotypically responds to the stop codon readthrough. </h4> </div> |
</div> | </div> | ||
Line 153: | Line 153: | ||
toprion2(); | toprion2(); | ||
toprion(); | toprion(); | ||
− | + | ||
+ | $(".tsc1").hide() | ||
+ | $(".tsc2").hide() | ||
+ | $(".tsc3").hide() | ||
+ | $(".tsc1").on("click", function(){ | ||
+ | $(".texticles1").slideToggle() | ||
+ | }) | ||
+ | $(".tsc2").on("click", function(){ | ||
+ | $(".texticles2").slideToggle() | ||
+ | }) | ||
+ | $(".tsc3").on("click", function(){ | ||
+ | $(".texticles3").slideToggle() | ||
+ | }) | ||
}) | }) | ||
</script> | </script> |
Revision as of 03:05, 19 October 2016
OFF to priON
Using stop codon read-through and CRISPR to explore S. cerevisiae prion mechanisms
Furthering the advancement of research into prions and neurodegenerative diseases
We initiate a [PSI+] response in S. cerevisiae using a plasmid that will overexpress Sup35-NM.
We insert a premature stop codon into an N-terminal CFP tag that will be read through and fluoresce during a [PSI+] response
We control read through rates by choosing the location of the premature stop codon, and can therefore control protein production in [PSI+]. We use Hsp104, a chaperone protein in S. cerevisiae, to demonstrate that our set-up phenotypically responds to the stop codon readthrough.