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Inhibition of Pyrimidine Dimer Formation in DNA by Cationic Molecules: Role of Energy Transfer

*Corresponding author for this work
  • Unknown
Scholary Output:
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Article
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Open access

Abstract

In addition to the acridine dyes, acridine orange and proflavine, we find that three other cationic molecules which bind to DNA—ethidium bromide, chloroquine, and methyl green—inhibit the production of cyclobutyl pyrimidine dimers by ultraviolet radiation. Intercalation is not necessary for dimer inhibition. The long range nature of the inhibition implies that energy transfer is responsible. The transfer is between the lowest excited singlet state of DNA and the acceptor singlet, and seems to involve the Förster mechanism.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 1045-1055 (11 pages)

Journal (Volume, Issue Number)

Biophysical Journal (Volume 9, Issue 8)

Publication milestones

  • Published - 1969

Publication status

Published - 1969

ISSN

0006-3495

Publication IDs

  • Scopus: 0014559325
  • PubMed: 5822428

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Scopus
citations
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
1

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