Evaluation of three different formats of a neutralizing single chain human antibody against toxin Cn2: Neutralization capacity versus thermodynamic stability

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• 作者：Veronica Quintero-Herná ; ndez^a ; ^{vquinter@ibt.unam.mx} ; Luis Del Pozo-Yauner^b ; ^{ldelpozo@inmegen.gob.mx} ; Martha Pedraza-Escalona^a ; ^{mapedmx@ibt.unam.mx} ; Victor R. Juá ; rez-Gonzá ; lez^a ; ^{rivelino@ibt.unam.mx} ; Israel Alcá ; ntara-Recillas^a ; ^{ari_194@hotmail.com} ; Lourival D. Possani^a ; ^{possani@ibt.unam.mx} ; Baltazar Becerril^a ; ^{baltazar@ibt.unam.mx}
• 关键词：CDR ; complementary determining region ; CH ; constant domain heavy chain ; CL ; constant domain light chain ; ELISA ; enzyme-linked immunosorbent assay ; FR ; framework region ; KD ; dissociation constant ; RMSD ; root mean square deviation ; SCM ; spectra center of ma
• 刊名：Immunology Letters
• 出版年：2012
• 期刊代码：115_01652478
• 类别：med
• 出版时间：30 April, 2012
• 卷：143
• 期：2
• 页码：152-160
• 文件大小：797 K

摘要

The single-chain antibody fragment (scFv) 6009F, obtained by directed evolution, neutralizes the effects of the Cn2 toxin, which is the major toxic component of Centruroides noxius scorpion venom. In this work we compared the neutralization capacity and the thermodynamic stability of scFv 6009F with those of two other derived formats: Fab 6009F and diabody 6009F. Additionally, the affinity constants to Cn2 toxin of the three recombinant antibody fragments were determined by means of BIAcore. We found a correlation between the thermodynamic stability of these antibody fragments with their neutralization capacity. The order of thermodynamic stability determined was Fab 鈮?#xA0;scFv > diabody. The Fab and scFv were capable of neutralizing the toxic effects of Cn2 and whole venom but the diabody was unable to fully neutralize intoxication. In silico analysis of the diabody format indicates that the reduction of stability and neutralization capacity could be explained by a less cooperative interface between the heavy and the light variable domains.