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Ultraviolet irradiation of nucleic acids: formation, purification, and solution conformational analyses of the Cis-Syn and trans-syn photodimers of UpU

Journal Article · · Biochemistry; (United States)
DOI:https://doi.org/10.1021/bi00409a005· OSTI ID:7240803
Uridylyl(3'-5')uridine (UpU) is subjected to aqueous acetone photosensitized radiation with sunlamps. These irradiation conditions form only cyclobutane-type photodimers. Purification of a specific configurational photodimer is accomplished by using C-18 reverse-phase high-performance liquid chromatography. Multinuclear NMR analysis is used to analyze photoproduct formation and to determine conformational features of these photodimers. Four photodimers are identified, with the cis-syn isomer predominant. The cis-syn and trans-syn photodimers of UpU exhibit markedly different furanose and exocyclic bond conformations. A comparison of the properties of the cis-syn dimers of UpU with those of dTpdT reveal many similar conformational features but also some that are different.
Research Organization:
Roswell Park Memorial Institute, Buffalo, NY (USA)
OSTI ID:
7240803
Journal Information:
Biochemistry; (United States), Journal Name: Biochemistry; (United States) Vol. 27:9; ISSN BICHA
Country of Publication:
United States
Language:
English