Enhancement of stability of 7 beta,8 alpha-dihyroxy-9 alpha epoxybenzo(a)pyrene by complex formation with serum albumin.

C. J. Roche, D. Zinger, Nicholas Geacintov, R. G. Harvey

Research output: Contribution to journalArticle

Abstract

The biologically active and chemically unstable metabolite of benzo(a)pyrene, 7 beta,8 alpha-dihydroxy-9 alpha, 10 alpha-epoxybenzo(a)pyrene (BPDE), binds to human serum albumin in aqueous solutions with an association constant of 2.6 X 10(5)M-1. At pH 7.2, 24 degrees C and in 5mM sodium cacodylate buffer solution, this binding increases the lifetime of the diol epoxide by a factor of nearly 3. It is suggested that the formation of such physical complexes with proteins having hydrophobic interiors or with lipids may provide a mechanism by which highly reactive metabolites are transported from the site of metabolic synthesis to biological target molecules (e.g., DNA), in a reactive aqueous environment.

Original languageEnglish (US)
Pages (from-to)35-40
Number of pages6
JournalCancer Biochemistry Biophysics
Volume8
Issue number1
StatePublished - Jun 1985

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Serum Albumin
7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide
Cacodylic Acid
Benzo(a)pyrene
Epoxy Compounds
Buffers
Sodium
Lipids
DNA
Proteins
pyrene

ASJC Scopus subject areas

  • Biophysics
  • Cancer Research

Cite this

Enhancement of stability of 7 beta,8 alpha-dihyroxy-9 alpha epoxybenzo(a)pyrene by complex formation with serum albumin. / Roche, C. J.; Zinger, D.; Geacintov, Nicholas; Harvey, R. G.

In: Cancer Biochemistry Biophysics, Vol. 8, No. 1, 06.1985, p. 35-40.

Research output: Contribution to journalArticle

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