针对金属结合蛋白 MtsA 的新型格式 scFv×VHH 单链双抗体的表征。

IF 4.5 3区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Protein Science Pub Date : 2024-06-01 DOI:10.1002/pro.5017
Risa Asano, Miyu Takeuchi, Makoto Nakakido, Sho Ito, Chihiro Aikawa, Takeshi Yokoyama, Akinobu Senoo, Go Ueno, Satoru Nagatoishi, Yoshikazu Tanaka, Ichiro Nakagawa, Kouhei Tsumoto
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引用次数: 0

摘要

双特异性抗体(bpAbs)是一种工程化抗体,能与同一抗原中的多个不同表位结合。bpAbs 有多种形式,包括基于片段的形式,而针对目标分子的所需功能选择适当的分子形式是一项具有挑战性的任务。此外,优化构建体的设计需要选择适当的抗体模式并调整单个 bpAbs 的连接长度。因此,了解 bpAbs 在分子水平上的特性至关重要。在这项研究中,我们首先获得了针对金属结合蛋白MtsA不同表位的单链可变片段和驼科动物重链可变结构域,然后开发了一种新型格式的单链bpAb,将这些片段抗体与不同的连接体连接起来。我们采用多种方法分析了 bpAb 的理化性质、结合活性、与抗原形成复合物的状态以及功能。值得注意的是,我们发现复合物的组装状态受连接体控制,较长的连接体倾向于形成更紧凑的复合物。这些观察结果提供了详细的分子信息,在设计 bpAb 时应加以考虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterization of a novel format scFv×VHH single-chain biparatopic antibody against metal binding protein MtsA.

Biparatopic antibodies (bpAbs) are engineered antibodies that bind to multiple different epitopes within the same antigens. bpAbs comprise diverse formats, including fragment-based formats, and choosing the appropriate molecular format for a desired function against a target molecule is a challenging task. Moreover, optimizing the design of constructs requires selecting appropriate antibody modalities and adjusting linker length for individual bpAbs. Therefore, it is crucial to understand the characteristics of bpAbs at the molecular level. In this study, we first obtained single-chain variable fragments and camelid heavy-chain variable domains targeting distinct epitopes of the metal binding protein MtsA and then developed a novel format single-chain bpAb connecting these fragment antibodies with various linkers. The physicochemical properties, binding activities, complex formation states with antigen, and functions of the bpAb were analyzed using multiple approaches. Notably, we found that the assembly state of the complexes was controlled by a linker and that longer linkers tended to form more compact complexes. These observations provide detailed molecular information that should be considered in the design of bpAbs.

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来源期刊
Protein Science
Protein Science 生物-生化与分子生物学
CiteScore
12.40
自引率
1.20%
发文量
246
审稿时长
1 months
期刊介绍: Protein Science, the flagship journal of The Protein Society, is a publication that focuses on advancing fundamental knowledge in the field of protein molecules. The journal welcomes original reports and review articles that contribute to our understanding of protein function, structure, folding, design, and evolution. Additionally, Protein Science encourages papers that explore the applications of protein science in various areas such as therapeutics, protein-based biomaterials, bionanotechnology, synthetic biology, and bioelectronics. The journal accepts manuscript submissions in any suitable format for review, with the requirement of converting the manuscript to journal-style format only upon acceptance for publication. Protein Science is indexed and abstracted in numerous databases, including the Agricultural & Environmental Science Database (ProQuest), Biological Science Database (ProQuest), CAS: Chemical Abstracts Service (ACS), Embase (Elsevier), Health & Medical Collection (ProQuest), Health Research Premium Collection (ProQuest), Materials Science & Engineering Database (ProQuest), MEDLINE/PubMed (NLM), Natural Science Collection (ProQuest), and SciTech Premium Collection (ProQuest).
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