Characterization of multiple nicotinic acetylcholine receptor-binding proteins and phospholipases A(2) from the venom of the coral snake Micrurus nigrocinctus nigrocinctus

被引:46
作者
AlapeGiron, A
Stiles, B
Schmidt, J
GironCortes, M
Thelestam, M
Jornvall, H
Bergman, T
机构
[1] KAROLINSKA INST,DEPT MED BIOCHEM & BIOPHYS,S-17177 STOCKHOLM,SWEDEN
[2] UNIV COSTA RICA,FAC MED,DEPT BIOQUIM,SAN JOSE,COSTA RICA
[3] UNIV COSTA RICA,FAC MICROBIOL,INST CLODOMIRO PICADO,SAN JOSE,COSTA RICA
[4] USAMRIID,TOXINOL DIV,FREDERICK,MD
[5] KAROLINSKA INST,MICROBIOL & TUMORBIOL CTR,STOCKHOLM,SWEDEN
关键词
phospholipase A(2); neurotoxin; HPLC; monoclonal antibody; amino acid sequence; Micrurus;
D O I
10.1016/0014-5793(95)01543-4
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 presence of multiple nicotinic acetylcholine receptor (AchR)-binding proteins and phospholipases A(2) was detected in the venom of a member of the Elapinae subfamily, Micrurus nigrocinctus nigrocinctus. Multi-step chromatographies were used to isolate four AchR-binding proteins (Mnn-9, Mnn-4, Mnn-3C and Mnn-1A) and five basic PLA(2)s (nigroxins A, B, C1, C2 and C3), The Micrurus as AchR-binding proteins are antigenically and structurally related to short- and long-chain cu-neurotoxins from Naja. The nigroxins are antigenically similar and constitute a new antigenic subclass of PLA(2)s. Nigroxins A and B are class I PLA(2)s, structurally more related to enzymes from Bungarinae than to those from Hydrophinae/Laticaudinae. These data contribute to clarify the relationships between Micrurus venom proteins and other elapid toxins and may be useful to improve the neutralizing efficiency of antivenoms.
引用
收藏
页码:29 / 32
页数:4
相关论文
共 22 条
[1]   IMMUNOCHEMICAL CHARACTERIZATION OF MICRURUS-NIGROCINCTUS-NIGROCINCTUS VENOM WITH MONOCLONAL AND POLYCLONAL ANTIBODIES [J].
ALAPEGIRON, A ;
GUSTAFSSON, B ;
LOMONTE, B ;
THELESTAM, M ;
GUTIERREZ, JM .
TOXICON, 1994, 32 (06) :695-712
[2]   ELECTROPHORETIC AND IMMUNOCHEMICAL STUDIES OF MICRURUS SNAKE-VENOMS [J].
ALAPEGIRON, A ;
LOMONTE, B ;
GUSTAFSSON, B ;
DASILVA, NJ ;
THELESTAM, M .
TOXICON, 1994, 32 (06) :713-723
[3]  
ALAPEGIRON A, IN PRESS TOXICON
[4]   DIRECT ANALYSIS OF PEPTIDES AND AMINO-ACIDS FROM CAPILLARY ELECTROPHORESIS [J].
BERGMAN, T ;
AGERBERTH, B ;
JORNVALL, H .
FEBS LETTERS, 1991, 283 (01) :100-103
[5]  
Bolanos R, 1980, Bol Oficina Sanit Panam, V88, P189
[6]   CHARACTERIZATION OF ELAPIDAE SNAKE-VENOM COMPONENTS USING OPTIMIZED REVERSE-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC CONDITIONS AND SCREENING ASSAYS FOR ALPHA-NEUROTOXIN AND PHOSPHOLIPASE-A2 ACTIVITIES [J].
BOUGIS, PE ;
MARCHOT, P ;
ROCHAT, H .
BIOCHEMISTRY, 1986, 25 (22) :7235-7243
[7]   CLASSIFICATION OF PHOSPHOLIPASES-A2 ACCORDING TO SEQUENCE - EVOLUTIONARY AND PHARMACOLOGICAL IMPLICATIONS [J].
DUFTON, MJ ;
HIDER, RC .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1983, 137 (03) :545-551
[8]  
ENDO T, 1991, SNAKE TOXINS, P91
[9]   THE ABILITY OF SPECIFIC ANTIVENOM AND LOW-TEMPERATURE TO INHIBIT THE MYOTOXICITY AND NEUROMUSCULAR BLOCK INDUCED BY MICRURUS-NIGROCINCTUS VENOM [J].
GOULARTE, FC ;
CRUZHOFLING, MA ;
COGO, JC ;
GUTIERREZ, JM ;
RODRIGUESSIMIONI, L .
TOXICON, 1995, 33 (05) :679-689
[10]   AN ALTERNATIVE INVITRO METHOD FOR TESTING THE POTENCY OF THE POLYVALENT ANTIVENOM PRODUCED IN COSTA-RICA [J].
GUTIERREZ, JM ;
AVILA, C ;
ROJAS, E ;
CERDAS, L .
TOXICON, 1988, 26 (04) :411-413