Unnatural Ligands for Engineered Proteins: New Tools for Chemical Genetics

Author:

Bishop Anthony1,Buzko Oleksandr1,Heyeck-Dumas Stephanie1,Jung Ilyoung1,Kraybill Brian1,Liu Yi1,Shah Kavita1,Ulrich Scott1,Witucki Laurie1,Yang Feng1,Zhang Chao1,Shokat Kevan M.1

Affiliation:

1. Department of Chemistry, Princeton University, Princeton, New Jersey 08544;

Abstract

▪ Abstract  Small molecules that modulate the activity of biological signaling molecules can be powerful probes of signal transduction pathways. Highly specific molecules with high affinity are difficult to identify because of the conserved nature of many protein active sites. A newly developed approach to discovery of such small molecules that relies on protein engineering and chemical synthesis has yielded powerful tools for the study of a wide variety of proteins involved in signal transduction (G-proteins, protein kinases, 7-transmembrane receptors, nuclear hormone receptors, and others). Such chemical genetic tools combine the advantages of traditional genetics and the unparalleled temporal control over protein function afforded by small molecule inhibitors/activators that act at diffusion controlled rates with targets.

Publisher

Annual Reviews

Subject

Structural Biology,Biophysics

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