Interstrand psoralen cross-links do not introduce appreciable bends in DNA

Richard R. Sinden, Paul J Hagerman

Research output: Contribution to journalArticle

45 Citations (Scopus)

Abstract

Analysis of the X-ray crystallographic structure of an 8-methoxypsoralen-thymine monoadduct has led to the suggestion that psoralen cross-links would bend DNA by as much as 70° [Peckler, S., Graves, B., Kanne, D., Rapoport, H., Hearst, J. E., & Kim, S.-H. (1982) J. Mol. Biol. 162, 157-172]. DNA can exist in a stably bent configuration in solution as recently demonstrated from analysis of polyacrylamide gel electrophoresis and differential decay of birefringence. Using these techniques, we have investigated the structure of DNA cross-linked with 8-methoxypsoralen and 4,5′,8-trimethylpsoralen. The results are not consistent with cross-links introducing any appreciable stable bend in double-stranded DNA molecules. Results suggest that photobound 4,5′,8-trimethylpsoralen molecules lengthen DNA by the equivalent of about one base pair per photobound adduct. We have also determined that 4,5′,8-trimethylpsoralen cross-links are introduced preferentially into 5′-TA compared to 5′-AT DNA sequences.

Original languageEnglish (US)
Pages (from-to)6299-6303
Number of pages5
JournalBiochemistry
Volume23
Issue number26
StatePublished - 1984
Externally publishedYes

Fingerprint

Ficusin
Trioxsalen
DNA
Methoxsalen
Birefringence
Molecules
Thymine
DNA sequences
Electrophoresis
Base Pairing
Polyacrylamide Gel Electrophoresis
X-Rays
X rays

ASJC Scopus subject areas

  • Biochemistry

Cite this

Interstrand psoralen cross-links do not introduce appreciable bends in DNA. / Sinden, Richard R.; Hagerman, Paul J.

In: Biochemistry, Vol. 23, No. 26, 1984, p. 6299-6303.

Research output: Contribution to journalArticle

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