盘卷肽片 (CCPT):利用多价肽大环扩展肽构件设计

IF 14.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Journal of the American Chemical Society Pub Date : 2024-10-25 DOI:10.1021/jacs.4c0953110.1021/jacs.4c09531
Anthony R. Perez, Adekunle Adewole, Daphney Sihwa, Michael E. Colvin and Andrea D. Merg*, 
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引用次数: 0

摘要

肽具有易合成性和蛋白质模拟特性,是一种极具吸引力的生物分子构件,可用于制造具有新特性和新功能的人工仿生材料。在这里,我们通过揭示新型多价肽大环(96mers)的设计、合成和表征,扩展了肽构筑基块的设计空间。CCPTs 由多个正交的线圈肽域组成,这些肽域由柔性连接体分隔。环化产生的约束条件使 CCPTs 能够引导 CCPTs 的盘绕线圈形成 "边缘 "结构域与其自由肽结合伙伴之间进行可编程的多向相互作用。这些完全合成的构建体是通过本机化学连接和 Sortase A 介导的环化相结合的聚合合成策略组装而成的。圆二色性(CD)研究显示,沿 CCPT 边缘的环化和随后形成的线圈增加了螺旋稳定性。尺寸排阻色谱法(SEC)、分析型高效液相色谱法(HPLC)和荧光淬灭测定为各种组装的 CCPT 复合物提供了全面的生物物理表征,并证实了 CCPT 内的盘卷结构域与其设计的靶上游离肽伙伴之间的正交共定位。最后,我们采用分子动力学(MD)模拟作为理解 CCPTs 及其复合物结构动态的辅助方法,这种方法能从分子水平深入了解实验结果。对模拟的 CCPT 结构进行的 MD 分析揭示了 CCPT 在与其设计的结合伙伴发生复合(即形成盘绕线圈)时的僵化和膨胀,并为指导未来几代 CCPT 的设计提供了启示。将 CCPTs 加入基于盘绕线圈的构件库中,有可能通过解锁具有可设计的分子间界面的新拓扑结构来扩展盘绕线圈组装领域。
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Coiled Coil Peptide Tiles (CCPTs): Expanding the Peptide Building Block Design with Multivalent Peptide Macrocycles

Owing to their synthetic accessibility and protein-mimetic features, peptides represent an attractive biomolecular building block for the fabrication of artificial biomimetic materials with emergent properties and functions. Here, we expand the peptide building block design space through unveiling the design, synthesis, and characterization of novel, multivalent peptide macrocycles (96mers), termed coiled coil peptide tiles (CCPTs). CCPTs comprise multiple orthogonal coiled coil peptide domains that are separated by flexible linkers. The constraints, imposed by cyclization, confer CCPTs with the ability to direct programmable, multidirectional interactions between coiled coil-forming “edge” domains of CCPTs and their free peptide binding partners. These fully synthetic constructs are assembled using a convergent synthetic strategy via a combination of native chemical ligation and Sortase A-mediated cyclization. Circular dichroism (CD) studies reveal the increased helical stability associated with cyclization and subsequent coiled coil formation along the CCPT edges. Size-exclusion chromatography (SEC), analytical high-performance liquid chromatography (HPLC), and fluorescence quenching assays provide a comprehensive biophysical characterization of various assembled CCPT complexes and confirm the orthogonal colocalization between coiled coil domains within CCPTs and their designed on-target free peptide partners. Lastly, we employ molecular dynamics (MD) simulations, which provide molecular-level insights into experimental results, as a supporting method for understanding the structural dynamics of CCPTs and their complexes. MD analysis of the simulated CCPT architectures reveals the rigidification and expansion of CCPTs upon complexation, i.e., coiled coil formation with their designed binding partners, and provides insights for guiding the designs of future generations of CCPTs. The addition of CCPTs into the repertoire of coiled coil-based building blocks has the potential for expanding the coiled coil assembly landscape by unlocking new topologies having designable intermolecular interfaces.

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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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