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Nucleic Acids Research, 1989, Vol. 17, No. 3 955-967
© 1989


CHEMISTRY

A novel photoproduct of 2'-deoxyguanosine induced by acetone photosensitization: 8-(2,3,4-trihydroxybutyl)guanine

Narain D. Sharma, R. Jeremy, H. Davies*, Dennis R. Phillips1 and James A. McCloskey1

Biochemistry Department, Medical Biology Centre, Queen's University Belfast BT9 7BL, Northern Ireland 1Departments of Medicinal Chemistry and Biochemistry, University of Utah Salt Lake City, UT 84112, USA

*To whom correspondence should be addressed

Received November 8, 1988. Revised January 3, 1989. Accepted January 3, 1989.

Acetone photosensitisation of 2'-deoxyguanosine in deaerated aqueous solution gives 8-(2,3,4-trihydroxybutyl)guanine as a major photoproduct. Its structure and that of its tetraacetate have been determined primarily by high resolution 1H NMR and mass spectrometry; a di-isopropylidene derivative has also been prepared. Mechanistic aspects of this novel photochemical transformation are discussed, particularly in relation to the alkaline cleavage of acetone photosensitised DNA at the sites of guanine bases.


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