UNNATURAL LIGANDS FOR ENGINEERED PROTEINS: New Tools for Chemical Genetics
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 disc...
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Veröffentlicht in: | Annual review of biophysics and biomolecular structure 2000-01, Vol.29 (1), p.577-606 |
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Hauptverfasser: | , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | 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. |
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ISSN: | 1056-8700 1545-4266 |
DOI: | 10.1146/annurev.biophys.29.1.577 |