Identification of protective B-cell epitopes of Atroxlysin-I: A metalloproteinase from Bothrops atrox snake venom

被引:12
作者
Schneider, F. S. [1 ,2 ]
de Almeida Lima, S. [1 ]
Reis de Avila, G. [1 ]
Castro, K. L. [1 ]
Guerra-Duarte, C. [1 ]
Sanchez, E. F. [3 ]
Nguyen, C. [2 ]
Granier, C. [2 ]
Molina, F. [2 ]
Chavez-Olortegui, C. [1 ]
机构
[1] Univ Fed Minas Gerais, Inst Ciencias Biol, Dept Bioquim & Imunol, Belo Horizonte, MG, Brazil
[2] CNRS Alcediag, FRE 3690, Sys2Diag, Montpellier, France
[3] Fundacao Ezequiel Dias, Pesquisa & Desenvolvimento, Belo Horizonte, MG, Brazil
关键词
Linear B-cell epitope mapping; Snake venom metalloproteinases; Peptide synthesis; Hemorrhage; AMINO-ACID-SEQUENCE; LACHESIS-MUTA-MUTA; HEMORRHAGIC METALLOPROTEINASES; MONOCLONAL-ANTIBODIES; CRYSTAL-STRUCTURE; MUTALYSIN-II; PROTEIN; GENERATION; DAMAGE; COLLAGENASES;
D O I
10.1016/j.vaccine.2016.02.035
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Atroxlysin-I (Atr-I) is a hemorrhagic snake venom metalloproteinase (SVMP) from Bothrops atrox venom, the snake responsible for the majority of bites in the north region of South America. SVMPs like Atr-I produce toxic effects in victims including hemorrhage, inflammation, necrosis and blood coagulation deficiency. Mapping of B-cell epitopes in SVMPs might result in the identification of non-toxic molecules capable of inducing neutralizing antibodies and improving the anti-venom therapy. Here, using the SPOT-synthesis technique we identified two epitopes located in the N-ter region of Atr-I (AtrEp1-(22)YNGNSDKIRRRIHQM(36); and AtrEp2-(55)GVEIWSNKDLINVQ(68)). Based on the sequence of AtrEp1 and AtrEp2 a third peptide named Atr-I biepitope (AtrBiEp) was designed and synthesized ((23)NGNSDKIRRRIH(34)GG(55)GVEIWSNKDLINVQ(68)). AtrBiEp was used to immunize BALB/c mice. Anti-trBiEp serum cross-reacted against Atr-I in western blot and was able to fully neutralize the hemorrhagic activity of Atr-I. Our results provide a rational basis for the identification of neutralizing epitopes on Atr-I snake venom toxin and show that the use of synthetic peptides could improve the generation of immuno-therapeutics. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1680 / 1687
页数:8
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