An efficient approach for site-directed mutagenesis using central overlapping primers

被引:16
作者
Wang, Huiping [1 ,2 ]
Zhou, Nan [1 ,2 ]
Ding, Feng [1 ,2 ]
Li, Zhaofang [1 ,2 ]
Chen, Ruichuan [1 ,2 ]
Han, Aidong [1 ,2 ]
Liu, Runzhong [1 ,2 ]
机构
[1] Xiamen Univ, State Key Lab Cellular Stress Biol, Sch Life Sci, Xiamen 361005, Fujian, Peoples R China
[2] Xiamen Univ, Dept Biomed Sci, Sch Life Sci, Xiamen 361005, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
Site-directed mutagenesis; QuikChange; Central overlapping primers (COP); ENZYME EVOLUTION;
D O I
10.1016/j.ab.2011.07.008
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
QuikChange is a popular method for site-directed mutagenesis in structural and functional studies of proteins and nucleic acids. However, the standard protocol is often inefficient in producing the desired mutations. Here we present a novel strategy for primer design, central overlapping primers (COP), which employs a pair of bipartite primers of different lengths, with the short primer complementary to the middle region of the long primer. The COP method is efficient and robust in generating approximately 90% mutation rate without supercompetent Escherichia coli cells or laborious screening for positive clones. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:304 / 306
页数:3
相关论文
共 8 条
[1]   Phosphorylated positive transcription elongation factor b (P-TEFb) is tagged for inhibition through association with 7SK snRNA [J].
Chen, RC ;
Yang, ZY ;
Zhou, Q .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (06) :4153-4160
[2]   Random Mutagenesis Methods for In Vitro Directed Enzyme Evolution [J].
Labrou, Nikolaos E. .
CURRENT PROTEIN & PEPTIDE SCIENCE, 2010, 11 (01) :91-100
[3]   Quikgene: A gene synthesis method integrated with ligation-free cloning [J].
Mao, Yanjun ;
Lin, Juanyu ;
Zhou, Aibin ;
Ji, Kunmei ;
Downey, Jennifer S. ;
Chen, Ruichuan ;
Han, Aidong .
ANALYTICAL BIOCHEMISTRY, 2011, 415 (01) :21-26
[4]   The Yin and Yang of P-TEFb regulation: Implications for human immunodeficiency virus gene expression and global control of cell growth and differentiation [J].
Qiang Zhou ;
Yik, Jasper H. N. .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2006, 70 (03) :646-+
[5]   Milestones in directed enzyme evolution [J].
Tao, HY ;
Cornish, VW .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2002, 6 (06) :858-864
[6]   A novel megaprimed and ligase-free, PCR-based, site-directed mutagenesis method [J].
Tseng, Wen-Chi ;
Lin, Jing-Wei ;
Wei, Tsen-Yun ;
Fang, Tsuel-Yun .
ANALYTICAL BIOCHEMISTRY, 2008, 375 (02) :376-378
[7]   SITE-DIRECTED MUTAGENESIS OF DOUBLE-STRANDED DNA BY THE POLYMERASE CHAIN-REACTION [J].
WEINER, MP ;
COSTA, GL ;
SCHOETTLIN, W ;
CLINE, J ;
MATHUR, E ;
BAUER, JC .
GENE, 1994, 151 (1-2) :119-123
[8]   An efficient one-step site-directed and site-saturation mutagenesis protocol [J].
Zheng, L ;
Baumann, U ;
Reymond, JL .
NUCLEIC ACIDS RESEARCH, 2004, 32 (14) :e115