Next-generation antibodies for post-translational modifications

被引:35
|
作者
Hattori, Takamitsu [1 ,2 ]
Koide, Shohei [1 ,2 ,3 ]
机构
[1] NYU, Langone Med Ctr, Perlmutter Canc Ctr, 550 1st Ave, New York, NY 10016 USA
[2] NYU, Sch Med, Dept Biochem & Mol Pharmacol, New York, NY 10016 USA
[3] Univ Chicago, Dept Biochem & Mol Biol, 920 E 58th St, Chicago, IL 60637 USA
基金
美国国家卫生研究院;
关键词
PHAGE DISPLAY; HIGH-AFFINITY; PROTEIN-INTERACTION; STRUCTURAL BASIS; SURFACE DISPLAY; SPECIFICITY; ANTIGEN; DESIGN; SELECTION; SITE;
D O I
10.1016/j.sbi.2018.04.006
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
Despite increasing demands for antibodies to post translational modifications (PTMs), fundamental difficulties in molecular recognition of PTMs hinder the generation of highly functional anti-PTM antibodies using conventional methods. Recently, advanced approaches in protein engineering and design that have been established for biologics development were applied to successfully generating highly functional anti-PTM antibodies. Furthermore, structural analyses of anti-PTM antibodies revealed unprecedented binding modes that substantially increased the antigen-binding surface. These features deepen the understanding of mechanisms underlying specific recognition of PTMs, which may lead to more effective approaches for generating anti-PTM antibodies with exquisite specificity and high affinity.
引用
收藏
页码:141 / 148
页数:8
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