Protection of Mucuna pruriens seeds against Echis carinatus venom is exerted through a multiform glycoprotein whose oligosaccharide chains are functional in this role

被引:27
作者
Guerranti, R
Aguiyi, JC
Ogueli, IG
Onorati, G
Neri, S
Rosati, F
Del Buono, F
Lampariello, R
Pagani, R
Marinello, E
机构
[1] Univ Siena, Dipartimento Med Interna Sci Endocrino Metab & Bi, I-53100 Siena, Italy
[2] Univ Siena, Dipartimento Biol Evolut, I-53100 Siena, Italy
[3] Univ Siena, Dipartimento Chim, I-53100 Siena, Italy
[4] Univ Jos, Dept Pharmacol, Jos, Nigeria
关键词
plant extract; snake venom; glycoproteins; 2-D gel electrophoresis; N-linked oligosaccharides; carbohydrate epitopes;
D O I
10.1016/j.bbrc.2004.08.122
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
In a previous paper we demonstrated that extracts of Mucuna pruriens seeds (MPE) protect mice against Echis carinatus venom (EV) by an immunological mechanism. In this paper we demonstrate that the MPE immunogen generating the antibody that cross-reacts with the venom proteins is a multiform glycoprotein (gpMuc) whose immunogenic properties mainly reside in its glycanchains. The glycoprotein was purified from the protein extract of M. pruriens seeds using Concanavalin A affinity chromatography. Using 2-D gel electrophoresis it separated into seven isoforms having MWs in the range from 20.3 to 28.7 kDa and pIs from 4.8 to 6.5. N-terminal sequencing of these spots revealed close similarity since all of them contained the consensus sequence DDREPV-DT found in soybean Kunitz-type trypsin inhibitor. We suggest that gpMuc contains both N- and O-glycans. Mild alkaline treatment but not PNGase F led to loss of reactivity, indicating that O-glycans are probably involved in the antigenicity of gpMuc. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:484 / 490
页数:7
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