Making the most of affinity tags

被引:426
作者
Waugh, DS [1 ]
机构
[1] NCI, Prot Engn Sect, Macromol Crystallog Lab, Canc Res Ctr, Frederick, MD 21701 USA
关键词
D O I
10.1016/j.tibtech.2005.03.012
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Proteins do not naturally lend themselves to high-throughput analysis because of their diverse physiochemical properties. Consequently, affinity tags have become indispensable tools for structural and functional proteomics initiatives. Although originally developed to facilitate the detection and purification of recombinant proteins, in recent years it has become clear that affinity tags can have a positive impact on the yield, solubility and even the folding of their fusion partners. However, no single affinity tag is optimal with respect to all of these parameters; each has its strengths and weaknesses. Therefore, combinatorial tagging might be the only way to harness the full potential of affinity tags in a high-throughput setting.
引用
收藏
页码:316 / 320
页数:5
相关论文
共 44 条
[31]   Order of fusions between bacterial and mammalian proteins can determine solubility in Escherichia coli [J].
Sachdev, D ;
Chirgwin, JM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 244 (03) :933-937
[32]   USE OF PEPTIDE LIBRARIES TO MAP THE SUBSTRATE-SPECIFICITY OF A PEPTIDE-MODIFYING ENZYME - A 13 RESIDUE CONSENSUS PEPTIDE SPECIFIES BIOTINYLATION IN ESCHERICHIA-COLI [J].
SCHATZ, PJ .
BIO-TECHNOLOGY, 1993, 11 (10) :1138-1143
[33]  
SCHEIN CH, 1989, BIO-TECHNOL, V7, P1141
[34]   THE RANDOM PEPTIDE LIBRARY-ASSISTED ENGINEERING OF A C-TERMINAL AFFINITY PEPTIDE, USEFUL FOR THE DETECTION AND PURIFICATION OF A FUNCTIONAL IG FV FRAGMENT [J].
SCHMIDT, TGM ;
SKERRA, A .
PROTEIN ENGINEERING, 1993, 6 (01) :109-122
[35]   High-throughput screening of soluble recombinant proteins [J].
Shih, YP ;
Kung, WM ;
Chen, JC ;
Yeh, CH ;
Wang, AHJ ;
Wang, TF .
PROTEIN SCIENCE, 2002, 11 (07) :1714-1719
[36]   SINGLE-STEP PURIFICATION OF POLYPEPTIDES EXPRESSED IN ESCHERICHIA-COLI AS FUSIONS WITH GLUTATHIONE S-TRANSFERASE [J].
SMITH, DB ;
JOHNSON, KS .
GENE, 1988, 67 (01) :31-40
[37]   A plasmid expression system for quantitative in vivo biotinylation of thioredoxin fusion proteins in Escherichia coli [J].
Smith, PA ;
Tripp, BC ;
DiBlasio-Smith, EA ;
Lu, ZJ ;
LaVallie, ER ;
McCoy, JM .
NUCLEIC ACIDS RESEARCH, 1998, 26 (06) :1414-1420
[38]   Overview of tag protein fusions: from molecular and biochemical fundamentals to commercial systems [J].
Terpe, K .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2003, 60 (05) :523-533
[39]  
TROPEA JE, IN PRESS METHODS MOL
[40]  
Vaillancourt P, 2000, METHOD ENZYMOL, V326, P340