Kinetic Methods for Studying DNA Glycosylases Functioning in Base Excision Repair

被引:13
|
作者
Coey, Christopher T. [1 ]
Drohat, Alexander C. [1 ,2 ]
机构
[1] Univ Maryland, Sch Med, Baltimore, MD 21201 USA
[2] Univ Maryland, Sch Med, Marlene & Stewart Greenebaum Canc Ctr, Baltimore, MD 21201 USA
关键词
INTERSTRAND CROSS-LINKS; N-GLYCOSIDIC BOND; THYMINE-DNA; EXTINCTION COEFFICIENTS; ABASIC SITES; DUPLEX DNA; G.T MISPAIRS; 5-CARBOXYLCYTOSINE; ENDONUCLEASE-1; BINDING;
D O I
10.1016/bs.mie.2017.03.016
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Base excision repair (BER) is a conserved and ubiquitous pathway that is initiated by DNA glycosylases, which recognize and remove damaged or mismatched nucleobases, setting the stage for restoration of the correct DNA sequence by follow-on BER enzymes. DNA glycosylases employ a nucleotide-flipping step prior to cleavage of the N-glycosyl bond, and most exhibit slow release of the abasic DNA product and/or strong product inhibition. As such, studying the catalytic mechanism of these enzymes requires care in the design, execution, and interpretation of single-and multiple-turnover kinetics experiments, which is the topic of this chapter.
引用
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页码:357 / 376
页数:20
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