Tagging recombinant proteins with a Sel-tag for purification, labeling with electrophilic compounds or radiolabeling with 11C

被引:31
作者
Cheng, Qing
Stone-Elander, Sharon
Arner, Elias S. J. [1 ]
机构
[1] Karolinska Inst, Med Nobel Inst Biochem, Dept Med Biochem & Biophys, SE-17177 Stockholm, Sweden
[2] Karolinska Univ Hosp, SE-17176 Stockholm, Sweden
[3] Karolinska Inst, Dept Clin Neurosci, SE-17176 Stockholm, Sweden
关键词
D O I
10.1038/nprot.2006.87
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Selenocysteine ( Sec; U in one-letter code) is the twenty-first naturally occurring amino acid, with a selenium atom that gives this cysteine (Cys) homolog unique biochemical properties, including a high nucleophilicity and significant reactivity with electrophilic agents. This can be used in biotechnological Sec-dependent applications. Here, we describe how Sec can be introduced into a carboxy-terminal tetrapeptide motif (-Gly-Cys-Sec-Gly-COOH, known as a Sel-tag) for recombinant proteins by tailoring the encoding gene to become compatible with the Escherichia coli selenoprotein synthesis machinery. We also describe how the Sel-tag can be used as a basis for efficient one-step protein purification, rapid Sec-targeting protein labeling with electrophilic compounds, or radiolabeling with the positron emitter C-11.
引用
收藏
页码:604 / 613
页数:10
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