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Thermodynamics and kinetics for base pair opening in the DNA decamer duplexes containing cyclobutane pyrimidine dimer

Authors
Bang, JongchulKang, Young-MinPark, Chin-JuLee, Joon-HwaChoi, Byong-Seok
Issue Date
18-Jun-2009
Publisher
WILEY
Keywords
NMR; Hydrogen exchange rate; Cyclobutane pyrimidine dimer; XPC-hHR23B; Damage recognition
Citation
FEBS LETTERS, v.583, no.12, pp 2037 - 2041
Pages
5
Indexed
SCIE
SCOPUS
Journal Title
FEBS LETTERS
Volume
583
Number
12
Start Page
2037
End Page
2041
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/26275
DOI
10.1016/j.febslet.2009.05.015
ISSN
0014-5793
1873-3468
Abstract
The cyclobutane pyrimidine dimer (CPD) is one of the major classes of cytotoxic and carcinogenic DNA photoproducts induced by UV light. Hydrogen exchange rates of the imino protons were measured for various CPD-containing DNA duplexes to better understand the mechanism for CPD recognition by XPC-hHR23B. The results here revealed that double T.G mismatches in a CPD lesion significantly destabilized six consecutive base pairs compared to other DNA duplexes. This flexibility in a DNA duplex caused at the CPD lesions with double T.G mismatches might be the key factor for damage recognition by XPC-hHR23B. (C) 2009 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
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