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Article
Transforming ligands into transcriptional regulators: Building blocks for bifunctional molecules
Chemical Society Reviews
  • J. W. Højfeldt
  • Aaron R. Van Dyke, Fairfield University
  • Anna K. Mapp
Document Type
Article
Publication Date
1-1-2011
Abstract

The human body is comprised of several hundred distinct cell types that all share a common genomic template. This diversity arises from regulated expression of individual genes. The first critical step in this process is transcription and is governed by a large number of transcription factors. Small molecules that can alter transcription hold tremendous utility as chemical probes and therapeutics. To fully realize their potential, however, artificial transcription factors must be able to orchestrate protein recruitment at gene promoters just like their natural counterparts. This tutorial review surveys the discovery of small ligands (drug-like molecules and short peptides) that bind transcriptional coregulatory proteins, and thus comprise one of the two essential characteristics of a transcription factor. By joining these ligands to DNA-targeting moieties, one can construct a bifunctional molecule that recruits its protein target to specific genes and controls gene transcription.

Comments

Copyright 2011 Royal Society of Chemistry

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Published Citation
Højfeldt, J. W.; Van Dyke, A. R.; Mapp, A. K. "Transforming ligands into transcriptional regulators: Building blocks for bifunctional molecules". Chemical Society Reviews 40 (2011) pp. 4286–4294. DOI: 10.1039/C1CS15050B
DOI
DOI: 10.1039/C1CS15050B
Citation Information
J. W. Højfeldt, Aaron R. Van Dyke and Anna K. Mapp. "Transforming ligands into transcriptional regulators: Building blocks for bifunctional molecules" Chemical Society Reviews Vol. 40 (2011)
Available at: http://works.bepress.com/aaron_vandyke/4/