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Ribozyme chemogenetics
Author(s) -
Strobel Scott A.
Publication year - 1998
Publication title -
biopolymers
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.556
H-Index - 125
eISSN - 1097-0282
pISSN - 0006-3525
DOI - 10.1002/(sici)1097-0282(1998)48:1<65::aid-bip7>3.0.co;2-d
Subject(s) - ribozyme , chemistry , hairpin ribozyme , vs ribozyme , tetrahymena , stereochemistry , computational biology , hydrogen bond , rna , biochemistry , biology , molecule , organic chemistry , gene
In this review I will outline several chemogenetic approaches used to determine the chemical basis of large ribozyme function and structure. The term chemogenetics was first used to describe site‐specific functional group modification experiments in the analysis of DNA–protein interactions. Within the past few years equivalent experiments have been performed on large catalytic RNAs using both single‐site substitution and interference mapping techniques with nucleotide analogues. While functional group mutagenesis is an important aspect of a chemogenetic approach, chemical correlates to genetic revertants and suppressors must also be realized for the genetic analogy to be intellectually valid and experimentally useful. Several examples of functional group revertants and suppressors have now been obtained within the Tetrahymena group I ribozyme. These experiments define an ensemble of tertiary hydrogen bonds that have made it possible to construct a detailed model of the ribozyme catalytic core. The model includes a functionally important monovalent metal ion binding site, a wobble–wobble receptor motif for helix–helix packing interactions, and a minor groove triple helix. © 1998 John Wiley & Sons, Inc. Biopoly 48: 65–81, 1998