UMSI 2000 Annual Report: Karin M. Musier-Forsyth, Principal Investigator Previous Page  |  Table of Contents  |  Next Page

Karin M. Musier-Forsyth, Principal Investigator


tRNA Acceptor Stems

Research Group

Penny Beuning, Graduate Student Researcher
Stephanie Kerimo, Undergraduate Student Researcher


1999 UMSI Publications
99/111
"Wild-type RNA MicrohelixAla and 3:70 Variants: Molecular Dynamics Analysis of Local Helical Structure and Tightly Bound Water," M.C. Nagan, S.S. Kerimo, K. Musier-Forsyth, and C.J. Cramer, Journal of the American Chemical Society, 121, p. 7310 (1999).
A complete Bibliography can be found on the Internet at:
www.msi.umn.edu/cgi-bin/reports/searchv2.html

Molecular dynamics simulations of RNA microhelixAla indicate that G:U and other 3:70 purine:pyrimidine wobble pairs induce local deviations from A-form geometry in their respective microhelices; the helix is underwound at the base-pair step above and overwound at the base-pair step below, in each case by about 7 to 9 degrees compared to canonical A-form RNA. Based on analysis of average water densities and residence lifetimes, the wild-type microhelix strongly binds a water molecule in the minor groove of the 3:70 base pair, consistent with crystallographic analyses of an RNA duplex derived from the acceptor stem of Escherichia coli tRNAAla. Other wobble pairs show water binding at this position but to a lesser degree; the strength of water binding correlates directly with the measured aminoacylation activities of the microhelices as substrates for E. coli alanyl-tRNA synthetase. Watson-Crick base pairs at the 3:70 position show no tendency towards specific hydration. This tightly bound minor-groove water in the microhelices with 3:70 wobble pairs evidently does not function to stabilize a particular local helical structure, but it may play a role as a specific recognition element or serve as an indicator of interaction specificity between the microhelix and a hydroxylated residue of the aminoacyl-tRNA synthetase.


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