Sanchez Ambrocio, Buisson Rémi
Department of Biological Chemistry, School of Medicine, University of California Irvine, Irvine, California, United States; Chao Family Comprehensive Cancer Center, University of California Irvine, Irvine, California, United States; Center for Virus Research, University of California Irvine, Irvine, California, United States.
Department of Biological Chemistry, School of Medicine, University of California Irvine, Irvine, California, United States; Chao Family Comprehensive Cancer Center, University of California Irvine, Irvine, California, United States; Center for Virus Research, University of California Irvine, Irvine, California, United States; Department of Pharmaceutical Sciences, School of Pharmacy & Pharmaceutical Sciences, University of California Irvine, Irvine, California, United States.
Methods Enzymol. 2025;713:201-219. doi: 10.1016/bs.mie.2024.11.037. Epub 2024 Dec 7.
APOBEC enzymes promote the deamination of cytosine (C) to uracil (U) in DNA to defend cells against viruses but also serve as a predominant source of mutations in cancer genomes. This protocol describes an assay to monitor APOBEC deaminase activity in vitro on a synthetic DNA oligonucleotide. The method described here focuses specifically on APOBEC3B to illustrate the different steps of the assay. However, the protocol can be applied to monitor the DNA deaminase activity of any other member of the APOBEC family, such as APOBEC3A. This assay involves preparing APOBEC3B-expressing cell extract or purifying APOBEC3B by immunoprecipitation, followed by incubation with a single-stranded DNA containing a TpC motif. The deaminated cytosine is then removed by recombinant Uracil DNA Glycosylase present in the reaction to form an abasic site. The abasic site creates a weakness in the DNA's backbone, causing the DNA to be cleaved under high temperatures and alkaline conditions. Denaturing gel electrophoresis is used to separate cleaved DNA from full-length DNA, enabling the quantification of the percentage of deamination induced by APOBEC3B. This protocol can be used to determine the presence of APOBEC and the regulation of APOBEC activity in specific cell lines, to study substrate preference targeted by different members of the APOBEC family and different APOBEC mutants, or to determine the efficiency and specificity of inhibitor compounds against APOBEC enzymes.
载脂蛋白B mRNA编辑酶催化多肽(APOBEC)家族的酶可促使DNA中的胞嘧啶(C)脱氨基转变为尿嘧啶(U),以此保护细胞抵御病毒,但同时也是癌症基因组中突变的主要来源。本实验方案描述了一种在体外监测合成DNA寡核苷酸上APOBEC脱氨酶活性的检测方法。此处所述方法特别聚焦于APOBEC3B,以阐释该检测的不同步骤。不过,该方案可用于监测APOBEC家族其他任何成员的DNA脱氨酶活性,如APOBEC3A。此检测包括制备表达APOBEC3B的细胞提取物或通过免疫沉淀纯化APOBEC3B,随后与含有TpC基序的单链DNA一起孵育。然后,反应中存在的重组尿嘧啶DNA糖基化酶会去除脱氨基的胞嘧啶,形成一个无碱基位点。该无碱基位点会使DNA主链出现薄弱点,导致DNA在高温和碱性条件下被切割。变性凝胶电泳用于分离切割后的DNA与全长DNA,从而能够对APOBEC3B诱导的脱氨基百分比进行定量。本实验方案可用于确定特定细胞系中APOBEC的存在情况以及APOBEC活性的调控,研究APOBEC家族不同成员和不同APOBEC突变体靶向的底物偏好,或确定抑制剂化合物针对APOBEC酶的效率和特异性。