Sha Fern, Salzman Gabriel, Gupta Ankit, Koide Shohei
Department of Biochemistry and Molecular Biology, The University of Chicago, Chicago, Illinois, 60637.
Perlmutter Cancer Center, New York University Langone Medical Center, New York, NY, 10016.
Protein Sci. 2017 May;26(5):910-924. doi: 10.1002/pro.3148. Epub 2017 Mar 24.
Synthetic binding proteins are constructed using nonantibody molecular scaffolds. Over the last two decades, in-depth structural and functional analyses of synthetic binding proteins have improved combinatorial library designs and selection strategies, which have resulted in potent platforms that consistently generate binding proteins to diverse targets with affinity and specificity that rival those of antibodies. Favorable attributes of synthetic binding proteins, such as small size, freedom from disulfide bond formation and ease of making fusion proteins, have enabled their unique applications in protein science, cell biology and beyond. Here, we review recent studies that illustrate how synthetic binding proteins are powerful probes that can directly link structure and function, often leading to new mechanistic insights. We propose that synthetic proteins will become powerful standard tools in diverse areas of protein science, biotechnology and medicine.
合成结合蛋白是利用非抗体分子支架构建的。在过去二十年中,对合成结合蛋白的深入结构和功能分析改进了组合文库设计和筛选策略,从而产生了强大的平台,能够持续产生与各种靶标结合的蛋白,其亲和力和特异性可与抗体相媲美。合成结合蛋白的有利特性,如体积小、无需形成二硫键以及易于制备融合蛋白,使其在蛋白质科学、细胞生物学及其他领域具有独特的应用。在这里,我们回顾了最近的研究,这些研究表明合成结合蛋白是强大的探针,可以直接将结构与功能联系起来,常常能带来新的机制性见解。我们认为合成蛋白将成为蛋白质科学、生物技术和医学等不同领域的强大标准工具。