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PMID: 10937997 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

A single adenosine with a neutral pKa in the ribosomal peptidyl transferase center.

Science (New York, N.Y.) ·Vol. 289 ·No. 5481 ·2000-08-11 ·Pages 947-50

Muth GW, Ortoleva-Donnelly L, Strobel SA

Abstract

Biochemical and crystallographic evidence suggests that 23S ribosomal RNA (rRNA) is the catalyst of peptide bond formation. To explore the mechanism of this reaction, we screened for nucleotides in Escherichia coli 23S rRNA that may have a perturbed pKa (where Ka is the acid constant) based on the pH dependence of dimethylsulfate modification. A single universally conserved A (number 2451) within the central loop of domain V has a near neutral pKa of 7.6 +/- 0.2, which is about the same as that reported for the peptidyl transferase reaction. In vivo mutational analysis of this nucleotide indicates that it has an essential role in ribosomal function. These results are consistent with a mechanism wherein the nucleotide base of A2451 serves as a general acid base during peptide bond formation.

MeSH Terms
Adenosine/chemistry,metabolism Binding Sites Catalysis Dimethyl Sulfoxide Escherichia coli Hydrogen Bonding Methylation Mutation Peptide Biosynthesis Peptidyl Transferases/chemistry,metabolism Protons RNA, Bacterial/chemistry,genetics,metabolism RNA, Ribosomal, 23S/chemistry,genetics,metabolism Ribosomes/chemistry,metabolism Tubercidin/metabolism
Chemicals
Protons RNA, Bacterial RNA, Ribosomal, 23S 3-deazaadenosine Peptidyl Transferases Adenosine Tubercidin Dimethyl Sulfoxide
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Muth G W
Department of Molecular Biophysics and Biochemistry, Yale University, 260 Whitney Avenue, New Haven, CT 06520-8114, USA.
Ortoleva-Donnelly L
Strobel S A
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
2000-08-11
Pages
947-50
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIGMS NIH HHS · GM54839 · United States
Corrections
ErratumIn
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CommentIn
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