The post-genomic flood of genetic sequence information has already begun, and perhaps the largest task ahead is to place the myriads of newly-discovered biomolecules into functional context. The next generation of tools for genomic and proteomic analysis must work non-invasively and within the native cellular context. Capitalizing on recent advances in fluorescence technology and biopolymer engineering, this proposal describes three new generalizable methods for measuring RNA and protein function inside the living cell.
The specific aims are: (1) Development of genetically-encoded fluorescent reporters of enzyme activity in living cells. Specific application to the detection of histone kinase, acetyltransferase, and methyltransferase activities. (2) Development of ribozyme-based reporters for the detection of endogenous gene expression and endogenous protein-protein interactions in living cells. (3) Evolution of artificial enzymes for the site-specific labeling of proteins in living cells. The advantages offered by these methodologies over existing tools are two-fold: (a) minimally invasive applicability to any live cell culture rather than purified samples or heterologous systems, and (b) except for the site-specific labeling strategy described in Specific Aim 3, applicability to native genes and proteins, rather than fused reporter constructs. ? ? This research will be implemented by an investigator trained in chemical and biological techniques ranging from organic synthesis to molecular biology to live mammalian cell imaging. The investigator will develop a team of graduate students and postdoctoral researchers interested in working at the biology-chemistry interface to address long-standing biological problems on a genome-wide scale with molecular techniques. The chances of success will be maximized by execution of the proposed research in a chemistry department at a major research university. ? ?

Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Career Transition Award (K22)
Project #
1K22HG002671-01
Application #
6571384
Study Section
Ethical, Legal, Social Implications Review Committee (GNOM)
Program Officer
Felsenfeld, Adam
Project Start
2003-01-24
Project End
2004-12-31
Budget Start
2003-01-24
Budget End
2003-12-31
Support Year
1
Fiscal Year
2003
Total Cost
$263,760
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Howarth, Mark; Takao, Keizo; Hayashi, Yasunori et al. (2005) Targeting quantum dots to surface proteins in living cells with biotin ligase. Proc Natl Acad Sci U S A 102:7583-8
Chen, Irwin; Howarth, Mark; Lin, Weiying et al. (2005) Site-specific labeling of cell surface proteins with biophysical probes using biotin ligase. Nat Methods 2:99-104
Lin, Chi-Wang; Ting, Alice Y (2004) A genetically encoded fluorescent reporter of histone phosphorylation in living cells. Angew Chem Int Ed Engl 43:2940-3
Lin, Chi-Wang; Jao, Cindy Y; Ting, Alice Y (2004) Genetically encoded fluorescent reporters of histone methylation in living cells. J Am Chem Soc 126:5982-3