| Literature DB >> 9461074 |
C L Kielkopf1, E E Baird, P B Dervan, D C Rees.
Abstract
Small molecules that target specific DNA sequences offer a potentially general approach for the regulation of gene expression. Pyrrole-imidazole polyamides represent the only class of synthetic small molecules that can bind predetermined DNA sequences with affinities and specificities comparable to DNA binding proteins. Antiparallel side-by-side pairings of two aromatic amino acids, imidazole (Im) and pyrrole (Py), distinguish G.C from C.G, and both from A.T/T.A base pairs. A high resolution X-ray crystal structure of a four-ring pyrrole-imidazole polyamide specifically bound as a dimer to a six-base pair predetermined DNA site reveals a structural framework of hydrogen bonds and interactions with the walls of the minor groove that underlies the pairing rules for DNA recognition.Entities:
Mesh:
Substances:
Year: 1998 PMID: 9461074 DOI: 10.1038/nsb0298-104
Source DB: PubMed Journal: Nat Struct Biol ISSN: 1072-8368