Melee:mod4 proposal: Difference between revisions

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Shaner Paper on GFP Variants [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&dopt=AbstractPlus&list_uids=15558047&query_hl=3&itool=pubmed_docsum]
Shaner Paper on GFP Variants [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&dopt=AbstractPlus&list_uids=15558047&query_hl=3&itool=pubmed_docsum]
Zink Cytochrome C Oxidase Coupling [http://www.cnsi.ucla.edu/arr/paper?paper_id=196035]
Nakajime Ruthenium-Aqua Peper [www.ims.ac.jp/publications/ann_rev_99/ar199976.pdf]


=== Research Goals ===
=== Research Goals ===

Revision as of 08:32, 3 May 2007

Module 4, Research Proposal

Mike Lee and Mike Oh's research proposal for Module 4 of 20.109 Spring 2007.

Overview

We intend to explore the research done by Prof. Ed DeLong with proteorhodopsin in E. coli. The ultimate aim is to be able to harvest sunlight with proteorhodopsins for solar electrical purposes. We may later decide to focus on only one of the following aspects of our proposal, but there are a couple goals that we find to be essential for accomplishing our final objective. First, we would like to build a library of strains that are activated by different wavelengths of light, much in the way that Shaner, et al created strains of GFP that would fluoresce different colors. This would maximize the amount of sunlight harvested by the proteorhodopsins. The second goal is to create a mechanism that would transform the proton gradient created by the proteorhodopsins into an electrical current that could be hooked into a circuit.

Background

Proteorhodopsin is a light-activated protein that can produce a H+ gradient across a cell membrane. This gradient could be used as a source of energy. Proteorhodopsin is found in some marine microorganisms, and it has been successfully introduced into E. coli. Jan Liphardt at UC Berkeley observed E. coli with flagellar motors activated by green light.

Source: Technology Review [1]

Original Paper at PubMed [2]

Shaner Paper on GFP Variants [3]

Zink Cytochrome C Oxidase Coupling [4]

Nakajime Ruthenium-Aqua Peper [www.ims.ac.jp/publications/ann_rev_99/ar199976.pdf]

Research Goals

We would like to create a more flexible platform using proteorhodopsin where biologists could select a mutant that was sensitive to specific wavelengths of light.

Project Details and Methods

We will use directed evolution to create mutants and select for sensitivity to different wavelengths of light. (Shaner, et al) The electrical current will be created by either ruthenium-aqua complex (Nakajima, et al) or cytochrome c oxidase coupling (Zink).

Predictions

Resources needed