Deletion mutants of protective antigen that inhibit anthrax toxin both in vitro and in vivo

被引:9
作者
Ahuja, N [1 ]
Kumar, P [1 ]
Alam, S [1 ]
Gupta, M [1 ]
Bhatnagar, R [1 ]
机构
[1] Jawaharlal Nehru Univ, Ctr Biotechnol, New Delhi 110067, India
关键词
D O I
10.1016/S0006-291X(03)01227-0
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
The anthrax toxin complex is primarily responsible for most of the symptoms of anthrax. This complex is composed of three proteins, anthrax protective antigen, anthrax edema factor, and anthrax lethal factor. The three proteins act in binary combination of protective antigen plus edema factor (edema toxin) and protective antigen plus lethal factor (lethal toxin) that paralyze the host defenses and eventually kill the host. Both edema factor and lethal factor are intracellularly acting proteins that require protective antigen for their delivery into the host cell. In this study, we show that deletion of certain residues of protective antigen results in variants of protective antigen that inhibit the action of anthrax toxin both in vitro and in vivo. These mutants protected mice against both lethal toxin and edema toxin challenge, even when injected at a 1:8 ratio relative to the wild-type protein. Thus, these mutant proteins are promising candidates that may be used to neutralize the action of anthrax toxin. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:446 / 450
页数:5
相关论文
共 26 条
[1]   Rapid purification of recombinant anthrax-protective antigen under nondenaturing conditions [J].
Ahuja, N ;
Kumar, P ;
Bhatnagar, R .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 286 (01) :6-11
[2]   Anthrax toxin [J].
Bhatnagar, R ;
Batra, S .
CRITICAL REVIEWS IN MICROBIOLOGY, 2001, 27 (03) :167-200
[3]   Activation of phospholipase C and protein kinase C is required for expression of anthrax lethal toxin cytotoxicity in J774A.1 cells [J].
Bhatnagar, R ;
Ahuja, N ;
Goila, R ;
Batra, S ;
Waheed, SM ;
Gupta, P .
CELLULAR SIGNALLING, 1999, 11 (02) :111-116
[4]   ANTHRAX TOXIN - CHANNEL-FORMING ACTIVITY OF PROTECTIVE ANTIGEN IN PLANAR PHOSPHOLIPID-BILAYERS [J].
BLAUSTEIN, RO ;
KOEHLER, TM ;
COLLIER, RJ ;
FINKELSTEIN, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (07) :2209-2213
[5]   Identification of the cellular receptor for anthrax toxin [J].
Bradley, KA ;
Mogridge, J ;
Mourez, M ;
Collier, RJ ;
Young, JAT .
NATURE, 2001, 414 (6860) :225-229
[6]   Proteolytic inactivation of MAP-kinase-kinase by anthrax lethal factor [J].
Duesbery, NS ;
Webb, CP ;
Leppla, SH ;
Gordon, VM ;
Klimpel, KR ;
Copeland, TD ;
Ahn, NG ;
Oskarsson, MK ;
Fukasawa, K ;
Paull, KD ;
Vande Woude, GF .
SCIENCE, 1998, 280 (5364) :734-737
[7]   INHIBITORS OF RECEPTOR-MEDIATED ENDOCYTOSIS BLOCK THE ENTRY OF BACILLUS-ANTHRACIS ADENYLATE-CYCLASE TOXIN BUT NOT THAT OF BORDETELLA-PERTUSSIS ADENYLATE-CYCLASE TOXIN [J].
GORDON, VM ;
LEPPLA, SH ;
HEWLETT, EL .
INFECTION AND IMMUNITY, 1988, 56 (05) :1066-1069
[8]   Germination of Bacillus anthracis spores within alveolar macrophages [J].
Guidi-Rontani, C ;
Weber-Levy, M ;
Labruyère, E ;
Mock, M .
MOLECULAR MICROBIOLOGY, 1999, 31 (01) :9-17
[9]   Translocation of Bacillus anthracis lethal and oedema factors across endosome membranes [J].
Guidi-Rontani, C ;
Weber-Levy, M ;
Mock, M ;
Cabiaux, V .
CELLULAR MICROBIOLOGY, 2000, 2 (03) :259-264
[10]   ANTHRAX TOXIN PROTECTIVE ANTIGEN IS ACTIVATED BY A CELL-SURFACE PROTEASE WITH THE SEQUENCE SPECIFICITY AND CATALYTIC PROPERTIES OF FURIN [J].
KLIMPEL, KR ;
MOLLOY, SS ;
THOMAS, G ;
LEPPLA, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (21) :10277-10281