Identification of a cDNA encoding an active asparaginyl endopeptidase of Schistosoma mansoni and its expression in Pichia pastoris

被引:58
作者
Caffrey, CR
Mathieu, MA
Gaffney, AM
Salter, JP
Sajid, M
Lucas, KD
Franklin, C
Bogyo, M
McKerrow, JH
机构
[1] Univ Calif San Francisco, VAMC, Trop Dis Res Unit, San Francisco, CA 94121 USA
[2] Univ Calif San Francisco, VAMC, Dept Pathol, San Francisco, CA 94121 USA
[3] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94121 USA
关键词
asparaginyl endopeptides; legumain; Sm32; recombinant expression; Schistosoma;
D O I
10.1016/S0014-5793(99)01798-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Asparaginyl endopeptidases, or legumains, are a recently identified family of cysteine-class endopeptidases. A single gene encoding a Schistosoma mansoni asparaginyl endopeptidase (a.k.a. Sm32 or schistosome legumain) has been reported, but by sequence homology it would be expected to yield an inactive product as the active site C197 had been replaced by N. We now describe a new S. mansoni gene in which C197 is present. Both gene products were expressed in Pichia pastoris. Autocatalytic processing to fully active C197 Sm32 occurred at acid pH. in contrast, N197 Sm32 was not processed and this is consistent with the hypothesis that C197 is essential for catalysis. This was confirmed by mutation of N197 to C and re-expression in Pichia. The availability of recombinant active Sm32 allows detailed analysis of its catalytic mechanism and its function(s) in the biology of this important human parasite. (C) 2000 Federation of European Biochemical Societies.
引用
收藏
页码:244 / 248
页数:5
相关论文
共 17 条
[1]   Identification of the active site of legumain links it to caspases, clostripain and gingipains in a new clan of cysteine endopeptidases [J].
Chen, JM ;
Rawlings, ND ;
Stevens, RAE ;
Barrett, AJ .
FEBS LETTERS, 1998, 441 (03) :361-365
[2]   Cloning, isolation, and characterization of mammalian legumain, an asparaginyl endopeptidase [J].
Chen, JM ;
Dando, PM ;
Rawlings, ND ;
Brown, MA ;
Young, NE ;
Stevens, RA ;
Hewitt, E ;
Watts, C ;
Barrett, AJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (12) :8090-8098
[3]   Identification of human asparaginyl endopeptidase (legumain) as an inhibitor of osteoclast formation and bone resorption [J].
Choi, SJ ;
Reddy, SV ;
Devlin, RD ;
Menaa, C ;
Chung, HY ;
Boyce, BF ;
Roodman, GD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (39) :27747-27753
[4]  
CORMACK B, 1999, SHORT PROTOCOLS MOL, P8
[5]   Proregion structure of members of the papain superfamily. Mode of inhibition of enzymatic activity [J].
Cygler, M ;
Mort, JS .
BIOCHIMIE, 1997, 79 (11) :645-652
[6]  
DALTON JP, 1995, PARASITOLOGY, V111, P574
[7]  
DAVIS AH, 1987, J BIOL CHEM, V262, P12851
[8]   DEFINITION OF THE COMPLETE SCHISTOSOMA-MANSONI HEMOGLOBINASE MESSENGER-RNA SEQUENCE AND GENE-EXPRESSION IN DEVELOPING PARASITES [J].
ELMEANAWY, MA ;
AJI, T ;
PHILLIPS, NFB ;
DAVIS, RE ;
SALATA, RA ;
MALHOTRA, I ;
MCCLAIN, D ;
AIKAWA, M ;
DAVIS, AH .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1990, 43 (01) :67-78
[9]   A UNIQUE VACUOLAR PROCESSING ENZYME RESPONSIBLE FOR CONVERSION OF SEVERAL PROPROTEIN PRECURSORS INTO THE MATURE FORMS [J].
HARANISHIMURA, I ;
INOUE, K ;
NISHIMURA, M .
FEBS LETTERS, 1991, 294 (1-2) :89-93
[10]  
ISHII S-I, 1990, Journal of Protein Chemistry, V9, P294