Cell toxicity by ricin and elucidation of mechanism of Ricin inactivation

被引:19
|
作者
Meneguelli de Souza, L. C. [1 ]
de Carvalho, L. P. [2 ]
Araujo, J. S. [1 ]
de Melo, Ej. T. [2 ]
Machado, O. L. T. [1 ]
机构
[1] State Univ Northern Fluminense Darcy Ribeiro UENF, Ctr Biosci & Biotechnol, Lab Chem & Funct Prot & Peptides LQFPP, Av Alberto Lamego,2000 ZC, BR-28035200 Campos Dos Goytacazes, RJ, Brazil
[2] State Univ Northern Fluminense Darcy Ribeiro UENF, Ctr Biosci & Biotechnol, Lab Cell & Tissue Biol LBCT, Av Alberto Lamego,2000 ZC, BR-28035200 Campos Dos Goytacazes, RJ, Brazil
关键词
Ricin; Cytotoxicity; CaO treatment; Detoxification; OXIDATIVE STRESS; CASTOR; DETOXIFICATION; MEAL; DEGRADATION; CLEAVAGE; PROTEIN; DEATH; ABRIN;
D O I
10.1016/j.ijbiomac.2018.03.024
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
Castor cake is a by-product of the extraction of oil from from seeds of castor plants (Ricinus communis). This by-product contains high levels of proteins, but a toxic protein, ricin, limits its use as an animal feed. Ricin can be efficiently inactivated by treatment with calcium oxide (CaO), which can be evaluated by a cytotoxicity assay using LLC-MK2 cells. The mechanism by which the CaO treatment inactivates ricin, however, is unclear. We report the structural changes responsible for ricin inactivation. Purified ricin was treated with 0.6% CaO and then analyzed by mass spectrometry. This treatment degraded the ricin at preferential sites. The aqueous CaO solution had a pH >12, which preferentially cleaved asparagine residues, followed by glutamine, serine and glycine residues. The alkaline pH affected the tertiary structure of the ricin, cleaving its polypeptide chains and thereby eliminating its cytotoxic activity. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:821 / 828
页数:8
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