Nucleic Acid Interactions II. Chemical Linkage of the Carcinogen 3,4-Benzpyrene to DNA Induced by Photoradiation

The physical binding of benzpyrene-H3 with coil form of thymus DNA has been studied. Covalent linkage between the benzpyrene-H3 or the degradation products of benzpyrenc-H3 and DNA was generated by photoradiation at the absorption band of benzpyrene with the "yield" of photoproduct around 50%. This finding has been conclusively supported by experiments with precipitation and extraction, sedimentation, electrophoresis, spectroscopy, enzymic hydrolysis, and chromatography of the hydrolytic products.

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Publication Details

Journal
Caltech Library
Published
2026-08-13
DOI
https://doi.org/10.7907/dr6e-hb15
Primary Topic
DNA and Nucleic Acid Chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Nucleic Acid Interactions II. Chemical Linkage of the Carcinogen 3,4-Benzpyrene to DNA Induced by Photoradiation

Ponzy Lu, Paul On Pong Ts'o
Caltech Library
DNA and Nucleic Acid Chemistry
article

Nucleic Acid Interactions II. Chemical Linkage of the Carcinogen 3,4-Benzpyrene to DNA Induced by Photoradiation

Ponzy Lu, Paul On Pong Ts'o
article en

Abstract

The physical binding of benzpyrene-H3 with coil form of thymus DNA has been studied. Covalent linkage between the benzpyrene-H3 or the degradation products of benzpyrenc-H3 and DNA was generated by photoradiation at the absorption band of benzpyrene with the "yield" of photoproduct around 50%. This finding has been conclusively supported by experiments with precipitation and extraction, sedimentation, electrophoresis, spectroscopy, enzymic hydrolysis, and chromatography of the hydrolytic products.

Caltech Library
California Institute of Technology (US)
U.S. Public Health Service
Clean water and sanitation, Life below water
Openalex Percentile: Top 16%
DNA and Nucleic Acid Chemistry
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