发布: 2015年06月05日第5卷第11期 DOI: 10.21769/BioProtoc.1493 浏览次数: 8251
评审: Fanglian HeAnonymous reviewer(s)
Abstract
We previously reported enzymatic activity assays for the base excision repair (BER) enzymes DNA polymerase β (pol β), aprataxin (APTX), and flap endonuclease 1 (FEN1) in cell extracts from Saccharomyces cerevisiae (Çağlayan and Wilson, 2014). Here, we describe a method to prepare cell extracts from vertebrate cells to investigate these enzymatic activities for the processing of the 5´-adenylated-sugar phosphate-containing BER intermediate. This new protocol complements our previous publication. The cell lines used are wild-type and APTX-deficient human lymphoblast cells from an Ataxia with Oculomotor Apraxia Type 1 (AOA1) disease patient, wild-type and APTX-null DT40 chicken B cells, and mouse embryonic fibroblast (MEF) cells. This protocol is a quick and efficient way to make vertebrate cell extracts without using commercial kits.
Materials and Reagents
Equipment
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文章信息
版权信息
© 2015 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Çağlayan, M., Horton, J. K. and Wilson, S. H. (2015). Enzymatic Activity Assays for Base Excision Repair Enzymes in Cell Extracts from Vertebrate Cells. Bio-protocol 5(11): e1493. DOI: 10.21769/BioProtoc.1493.
分类
分子生物学 > DNA > DNA 损伤和修复
生物化学 > 蛋白质 > 活性
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