Production and activation of recombinant papain-like cysteine proteases

被引:107
作者
Brömme, D [1 ]
Nallaseth, FS
Turk, B
机构
[1] Mt Sinai Sch Med, Dept Human Genet, New York, NY 10029 USA
[2] Jozef Stefan Inst, Dept Biochem & Mol Biol, SI-1000 Ljubljana, Slovenia
关键词
cysteine proteases; papain-like; cathepsins; expression; activation; purification; Pichia; E; coli; baculovirus;
D O I
10.1016/S1046-2023(03)00212-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Papain-like cysteine proteases are the most numerous family of the cysteine protease class. They are expressed throughout the animal and plant kingdoms as well as in viruses and bacteria. More recently, this protease family has drawn attention as a potential pharmaceutical drug target in diseases characterized by excessive extracellular matrix degradation such as in osteoporosis, arthritis, vascular diseases, and cancer. Moreover, papain-like cysteine proteases have been identified as critical components of the life cycle and invasive potential of various human and live stock pathogens as well as major allergens. Therefore, this protease class is rigorously studied and requires sufficient amounts of protease protein to analyze structure-activity relationships, their 3-D structures as well as to screen for and optimize potent and selective inhibitors. This review summarizes approaches to generate active papain-like cysteine proteases by heterologous expression in a variety of expression systems. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:199 / 206
页数:8
相关论文
共 65 条
[51]  
SMITH EL, 1989, BONE MINERAL RES, V6, P139
[52]  
SMITH SM, 1989, J BIOL CHEM, V264, P20487
[53]   The crystal structure of human cathepsin F and its implications for the development of novel immunomodulators [J].
Somoza, JR ;
Palmer, JT ;
Ho, JD .
JOURNAL OF MOLECULAR BIOLOGY, 2002, 322 (03) :559-568
[54]   Characterization of recombinant human cathepsin B expressed at high levels in baculovirus [J].
Steed, PM ;
Lasala, D ;
Liebman, J ;
Wigg, A ;
Clark, K ;
Knap, AK .
PROTEIN SCIENCE, 1998, 7 (09) :2033-2037
[55]   USE OF BACTERIOPHAGE-T7 LYSOZYME TO IMPROVE AN INDUCIBLE T7 EXPRESSION SYSTEM [J].
STUDIER, FW .
JOURNAL OF MOLECULAR BIOLOGY, 1991, 219 (01) :37-44
[56]   ACTIVE PAPAIN RENATURED AND PROCESSED FROM INSOLUBLE RECOMBINANT PROPAPAIN EXPRESSED IN ESCHERICHIA-COLI [J].
TAYLOR, MAJ ;
PRATT, KA ;
REVELL, DF ;
BAKER, KC ;
SUMNER, IG ;
GOODENOUGH, PW .
PROTEIN ENGINEERING, 1992, 5 (05) :455-459
[57]   SENSITIVE QUANTITATIVE-ANALYSIS OF DISULFIDE BONDS IN POLYPEPTIDES AND PROTEINS [J].
THANNHAUSER, TW ;
KONISHI, Y ;
SCHERAGA, HA .
ANALYTICAL BIOCHEMISTRY, 1984, 138 (01) :181-188
[58]   Identification of in vitro folding conditions for procathepsin S and cathepsin S using fractional factorial screens [J].
Tobbell, DA ;
Middleton, BJ ;
Raines, S ;
Needham, MRC ;
Taylor, IWF ;
Beveridge, JY ;
Abbott, WM .
PROTEIN EXPRESSION AND PURIFICATION, 2002, 24 (02) :242-254
[59]  
VELASCO G, 1994, J BIOL CHEM, V269, P27136
[60]   PROCESSING OF THE PAPAIN PRECURSOR - THE IONIZATION STATE OF A CONSERVED AMINO-ACID MOTIF WITHIN THE PRO REGION PARTICIPATES IN THE REGULATION OF INTRAMOLECULAR PROCESSING [J].
VERNET, T ;
BERTI, PJ ;
DEMONTIGNY, C ;
MUSIL, R ;
TESSIER, DC ;
MENARD, R ;
MAGNY, MC ;
STORER, AC ;
THOMAS, DY .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (18) :10838-10846