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PMID: 6176270 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Dependence of 4'-(hydroxymethyl)-4,5',8-trimethylpsoralen photoaddition on the conformation of ribonucleic acid.

Biochemistry ·Vol. 21 ·No. 6 ·1982-03-16 ·Pages 1363-8

Thompson JF, Bachellerie JP, Hall K, Hearst JE

Abstract

The photoaddition of 4'-(hydroxymethyl)-4,5',8-trimethylpsoralen (HMT) to different conformational states of RNA was studied. Poly(U), poly(A,U) (random copolymer), poly(A-U) (alternating copolymer), poly(A) . poly(U) (double stranded), and poly(U) . poly(A) . poly(U) (triple stranded) were reacted with HMT at different temperatures and salt concentrations. The conformation of the polymers was monitored by UV absorption and circular dichroism. It was found that the rate of HMT photoaddition changed dramatically at structural transitions in the RNA. The alternating copolymer poly(A-U) was found to have the highest rate of addition. Low salt and temperature produced maximal incorporation.

MeSH Terms
Circular Dichroism Furocoumarins/metabolism Nucleic Acid Conformation Photochemistry Poly A/metabolism Poly A-U/metabolism Poly U/metabolism RNA/metabolism Spectrophotometry, Ultraviolet Trioxsalen/analogs & derivatives,metabolism
Chemicals
Furocoumarins Poly A-U Poly A Poly U hydroxymethyltrioxsalen RNA Trioxsalen
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Thompson J F
Bachellerie J P
Hall K
Hearst J E
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1982-03-16
Pages
1363-8
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Grants
NIGMS NIH HHS · GM 11180 · United States
NIGMS NIH HHS · GM 25936-01 · United States
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