Riaño-Umbarila Lidia, Juárez-González Victor Rivelino, Olamendi-Portugal Timoteo, Ortíz-León Mauricio, Possani Lourival Domingos, Becerril Baltazar
Department of Molecular Medicine and Bioprocesses, Institute of Biotechnology, National Autonomous University of Mexico, Cuernavaca, Mexico.
FEBS J. 2005 May;272(10):2591-601. doi: 10.1111/j.1742-4658.2005.04687.x.
This study describes the construction of a library of single-chain antibody fragments (scFvs) from a single human donor by individual amplification of all heavy and light variable domains (1.1 x 10(8) recombinants). The library was panned using the phage display technique, which allowed selection of specific scFvs (3F and C1) capable of recognizing Cn2, the major toxic component of Centruroides noxius scorpion venom. The scFv 3F was matured in vitro by three cycles of directed evolution. The use of stringent conditions in the third cycle allowed the selection of several improved clones. The best scFv obtained (6009F) was improved in terms of its affinity by 446-fold, from 183 nm (3F) to 410 pm. This scFv 6009F was able to neutralize 2 LD(50) of Cn2 toxin when a 1 : 10 molar ratio of toxin-to-antibody fragment was used. It was also able to neutralize 2 LD(50) of the whole venom. These results pave the way for the future generation of recombinant human antivenoms.
本研究描述了通过对所有重链和轻链可变区进行单独扩增(1.1×10⁸个重组体),构建来自单个人类供体的单链抗体片段(scFv)文库的过程。使用噬菌体展示技术对该文库进行淘选,从而筛选出能够识别墨西哥毒蝎毒液主要毒性成分Cn2的特异性scFv(3F和C1)。通过三轮定向进化在体外使scFv 3F成熟。在第三轮中使用严格条件筛选出了几个改进的克隆。获得的最佳scFv(6009F)的亲和力提高了446倍,从183 nM(3F)提高到410 pM。当毒素与抗体片段的摩尔比为1:10时,该scFv 6009F能够中和2个半数致死剂量(LD₅₀)的Cn2毒素。它还能够中和2个LD₅₀的全毒液。这些结果为未来重组人抗蛇毒血清的研发铺平了道路。