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Nature-inspired design of motif-specific antibody scaffolds

机译:大自然启发的基序特异性抗体支架设计

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摘要

Aberrant changes in post-translational modifications (PTMs) such as phosphorylation underlie a majority of human diseases. However, detection and quantification of PTMs for diagnostic or biomarker applications often requires monoclonal PTM-specific antibodies, which are challenging to generate using traditional antibody-generation platforms. Here we outline a general strategy for producing synthetic PTM-specific antibodies by engineering a motif-specific ‘hot spot’ into an antibody scaffold. Inspired by a natural phosphate-binding motif, we designed antibody scaffolds with hot spots specific for phosphoserine, phosphothreonine, or phosphotyrosine. Crystal structures of the phospho-specific antibodies revealed two distinct modes of phosphoresidue recognition. Our data suggest that each hot spot functions independently of the surrounding scaffold, as phage display antibody libraries using these scaffolds yielded >50 phospho- and target-specific antibodies against 70% of target peptides. Ultimately, our motif-specific scaffold strategy may provide a general solution for the rapid, robust development of monoclonal anti-PTM antibodies for signaling, diagnostic and therapeutic applications.
机译:翻译后修饰(PTM)中的异常变化(例如磷酸化)是大多数人类疾病的基础。然而,用于诊断或生物标志物应用的PTM的检测和定量通常需要单克隆PTM特异性抗体,使用传统的抗体生成平台很难产生PTM特异性抗体。在这里,我们概述了通过将基序特异性的“热点”改造成抗体支架来生产合成PTM特异性抗体的一般策略。受天然磷酸盐结合基序的启发,我们设计了具有磷酸丝氨酸,磷酸苏氨酸或磷酸酪氨酸特异性热点的抗体支架。磷酸特异性抗体的晶体结构揭示了两种不同的磷酸酯识别模式。我们的数据表明,每个热点的功能均独立于周围的支架,因为使用这些支架的噬菌体展示抗体库可产生针对50%的目标肽的> 50磷酸和目标特异性抗体。最终,我们的基序特异性支架策略可为信号转导,诊断和治疗应用的单克隆抗PTM抗体的快速,稳健发展提供一般解决方案。

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