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一种用于快速鉴定蛋白质-蛋白质相互作用和迭代蛋白质设计的多重化细菌双杂交系统。

A multiplexed bacterial two-hybrid for rapid characterization of protein-protein interactions and iterative protein design.

机构信息

Department of Chemistry and Biochemistry, University of California, Los Angeles, CA, 90095, USA.

Department of Synthetic Biology and Immunology, National Institute of Chemistry, 1000, Ljubljana, Slovenia.

出版信息

Nat Commun. 2023 Aug 2;14(1):4636. doi: 10.1038/s41467-023-38697-x.

Abstract

Protein-protein interactions (PPIs) are crucial for biological functions and have applications ranging from drug design to synthetic cell circuits. Coiled-coils have been used as a model to study the sequence determinants of specificity. However, building well-behaved sets of orthogonal pairs of coiled-coils remains challenging due to inaccurate predictions of orthogonality and difficulties in testing at scale. To address this, we develop the next-generation bacterial two-hybrid (NGB2H) method, which allows for the rapid exploration of interactions of programmed protein libraries in a quantitative and scalable way using next-generation sequencing readout. We design, build, and test large sets of orthogonal synthetic coiled-coils, assayed over 8,000 PPIs, and used the dataset to train a more accurate coiled-coil scoring algorithm (iCipa). After characterizing nearly 18,000 new PPIs, we identify to the best of our knowledge the largest set of orthogonal coiled-coils to date, with fifteen on-target interactions. Our approach provides a powerful tool for the design of orthogonal PPIs.

摘要

蛋白质-蛋白质相互作用 (PPIs) 对生物功能至关重要,其应用范围从药物设计到合成细胞电路。螺旋是一种用于研究特异性序列决定因素的模型。然而,由于正交性预测不准确以及大规模测试困难,构建表现良好的正交螺旋对仍然具有挑战性。为了解决这个问题,我们开发了下一代细菌双杂交 (NGB2H) 方法,该方法允许使用下一代测序读数以定量和可扩展的方式快速探索编程蛋白文库的相互作用。我们设计、构建和测试了大量的正交合成螺旋,对 8000 多个 PPI 进行了检测,并使用该数据集训练了更准确的螺旋评分算法 (iCipa)。在对近 18000 个新的 PPI 进行特征描述后,我们认为我们所知的迄今为止最大的一组正交螺旋是十五个靶标相互作用。我们的方法为设计正交 PPI 提供了一个强大的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77d8/10397247/613ae8226e1d/41467_2023_38697_Fig1_HTML.jpg

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