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PMID: 8418834 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Betaine can eliminate the base pair composition dependence of DNA melting.

Biochemistry ·Vol. 32 ·No. 1 ·1993-01-12 ·Pages 137-44

Rees WA, Yager TD, Korte J, von Hippel PH

Abstract

We show that the amino acid analogue betaine shares with small tetraalkylammonium ions [Melchior, W. B., Jr., & von Hippel, P. H. (1973) Proc. Natl. Acad. Sci. U.S.A. 70, 298-302] the ability to reduce or even eliminate the base pair composition dependence of DNA thermal melting transitions. The "isostabilizing" concentration of betaine (at which AT and GC base pairs are equally stable) is approximately 5.2 M. Betaine exerts its isostabilizing effect without appreciably altering the conformation of double-stranded DNA from the B form. The presence of > 5 M betaine also does not greatly change the behavior of DNA as a polyelectrolyte; this lack of effect on electrostatic interactions is expected because betaine exists as a zwitterion near neutral pH. Study of DNA melting transitions in high concentrations of betaine thus allows the experimental separation of compositional and polyelectrolyte effects on DNA melting. As a consequence, betaine solutions can also be used to investigate DNA-protein interactions under isostabilizing (or close to isostabilizing) conditions, which has not been possible using isostabilizing salts. This potential is illustrated by examining the highly salt concentration-dependent interaction of ribonuclease A with DNA in concentrated betaine solutions.

MeSH Terms
Base Composition Betaine/pharmacology DNA/chemistry,drug effects,metabolism DNA, Bacterial/chemistry,drug effects Electrochemistry Hot Temperature Nucleic Acid Conformation Poly dA-dT/metabolism Potassium Chloride/pharmacology Ribonuclease, Pancreatic/metabolism Thermodynamics
Chemicals
DNA, Bacterial Poly dA-dT Betaine Potassium Chloride DNA Ribonuclease, Pancreatic
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Rees W A
Institute of Molecular Biology, University of Oregon, Eugene 97403.
Yager T D
Korte J
von Hippel P H
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1993-01-12
Pages
137-44
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Grants
NIGMS NIH HHS · GM-10227 · United States
NIGMS NIH HHS · GM-15792 · United States
NIGMS NIH HHS · GM-29158 · United States
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