"
Team:Johns Hopkins/Project
From 2010.igem.org
SunPenguin (Talk | contribs) |
(→Results) |
||
| Line 78: | Line 78: | ||
== Results == | == Results == | ||
| + | [[Image:crz1-grp+movie+1|thumb|300px|A dissolve transition between two still images]] | ||
Revision as of 02:34, 16 October 2010
Contents |
In a Sentence...
We are engineering Saccharomyces cerevisiae to be voltage-sensitive at the transcriptional level.
Abstract
If the goal of iGEM and the Parts Registry is to take the messy world of genetic engineering and transform it into something like the standardized world of electrical engineering, it may be useful if electronic systems could directly interface with biological systems. Past iGEM projects have used chemical or optical stimuli to actuate transcriptional responses. Our project, however, seeks to add voltage sensitivity to Saccharomyces cerevisiae. Baker’s yeast was chosen because in some sense yeast have a system that responds to voltage input. With a voltage stimulus one can open the voltage-gated calcium channels of yeast, causing calcium ions to rush into the cytoplasm. This causes calcineurin to dephosphorylate Crz1, which enters the nucleus and binds various promoters. Our group presents a library of characterized Crz1-sensitive promoters of both naturally-occurring and synthetic varieties. Genes downstream of these promoters are thus voltage-regulated in media containing calcium.
