Coiled-coil Technology for Regulating Intracellular Protein-protein Interactions

用于调节细胞内蛋白质-蛋白质相互作用的卷曲螺旋技术

• 批准号: BB/V008412/1
• 负责人: Andrew Wilson
• 金额: $ 60.45万
• 依托单位: University of Leeds
• 依托单位国家: 英国
• 项目类别: Research Grant
• 财政年份: 2021
• 资助国家: 英国
• 起止时间: 2021 至 无数据
• 项目状态: 已结题
• 来源: https://gtr.ukri.org/projects?ref=BB%2FV008412%2F1
• 关键词: Coiled; coil; Technology; Regulating; Intracellular

Proteins are the workhorses of biology. Proteins rarely work alone, and they cooperative via so called protein-protein interactions. In this way, they form larger assemblies and networks of proteins. In turn, these provide frameworks for controlling all cellular processes that regulate life. Dysregulation of the underlying protein-protein interactions can result in disease. The scale of this framework of protein-protein interactions within a cell is enormous; it has been estimated to be around 650,000 different interactions. These present considerable opportunities for intervening in biological processes (a) to understand healthy cells better, and (b) to develop new therapeutics when subcellular mechanisms go wrong. There are different ways to do this. We propose a new approach that employs synthetic protein modules (i) to disrupt protein-protein interactions and (ii) to hijack endogenous cell machineries. Synthetic chemical probes-such as small-molecule drugs-function by binding to a protein target within the body. This can be used to interfere with the target protein's function to help understand its biological role and as a starting point for drug discovery. Most chemical probes bind to well-defined pockets in proteins; this is analogous to a key fitting into a lock. By contrast, the design of probes to interfere with protein-protein interactions generally requires a fundamentally different type of association between the probe and one of the interacting target proteins; analogous to a hand gripping a ball. Thus, the development of effective probes that target protein-protein interactions raises new challenges that need to be met in future chemical biology and drug discovery. Two emerging approaches are promising for this, and we propose to combine them in this grant application.The first is a synthetic-biology approach. This uses synthetic proteins called de novo coiled coils as scaffolds for building new protein-protein interactions from scratch. This is attractive because natural coiled-coil proteins exhibit an array of protein-recognition properties and we can design de novo coiled-coils with diverse structures thereby expanding their potential. The second involves the targeted destruction of cellular proteins; in essence, this is a search-and-destroy strategy that co-opts the cell's own waste-disposal machineries so as to block protein function or remove harmful proteins that cause disease. The proposed research will develop new methodologies (i) to disrupt specified protein-protein interactions and (ii) to target certain proteins of interest for degradation. In this way, we will regulate specified processes in cells. To do this, we will not use conventional small molecules as the probes for intervening in the underlying protein-protein interactions. Rather, we will employ the synthetic coiled coils and adapt these to recognise the target proteins. In addition, for the second application, the coiled coils will be modified further to link the target protein to the cell's degradation pathways. Our aim is to deliver methods and reagents that will be of use to others in studying biological function and for developing new drugs to treat disease.This work is necessarily interdisciplinary. Therefore, we bring together a team of computational and experimental chemists, biochemists and cell biologists to tackle it, and we partner with a biotech company to translate the work in timely and relevant manner.

蛋白质是生物学的主力。蛋白质很少单独工作，它们通过所谓的蛋白质-蛋白质相互作用进行合作。通过这种方式，它们形成了更大的蛋白质组装和网络。反过来，它们提供了控制所有调节生命的细胞过程的框架。潜在的蛋白质-蛋白质相互作用的失调可能导致疾病。这个细胞内蛋白质-蛋白质相互作用框架的规模是巨大的；据估计，它大约有650,000种不同的相互作用。这为干预生物学过程提供了相当大的机会(A)更好地了解健康细胞，以及(B)在亚细胞机制出错时开发新的治疗方法。有不同的方法可以做到这一点。我们提出了一种新的方法，使用合成蛋白质模块(I)来扰乱蛋白质-蛋白质相互作用和(II)劫持内源细胞机器。合成化学探针--如小分子药物--通过与体内的蛋白质靶标结合而发挥作用。这可以用来干扰目标蛋白的功能，以帮助理解其生物学作用，并作为药物发现的起点。大多数化学探针结合在蛋白质中定义明确的口袋上；这类似于将钥匙插入锁中。相比之下，设计用于干扰蛋白质-蛋白质相互作用的探针通常需要在探针和其中一个相互作用的目标蛋白质之间建立根本不同类型的结合；类似于手抓球。因此，针对蛋白质相互作用的有效探针的开发提出了未来化学生物学和药物发现需要应对的新挑战。两种新兴的方法在这方面很有希望，我们建议在这次拨款申请中结合这两种方法。第一种是合成生物学方法。这项研究使用一种名为新卷曲的合成蛋白质作为支架，从头开始构建新的蛋白质-蛋白质相互作用。这是很有吸引力的，因为天然的卷曲蛋白展示了一系列的蛋白质识别特性，我们可以设计出具有不同结构的从头开始的卷曲蛋白质，从而扩大它们的潜力。第二种方法涉及对细胞蛋白质的定向破坏；本质上，这是一种搜索和破坏策略，它利用细胞自身的废物处理机制来阻止蛋白质功能或移除导致疾病的有害蛋白质。拟议的研究将开发新的方法(I)破坏特定的蛋白质-蛋白质相互作用和(Ii)针对某些感兴趣的蛋白质进行降解。通过这种方式，我们将调节细胞中特定的过程。要做到这一点，我们不会使用传统的小分子作为探针来干预潜在的蛋白质-蛋白质相互作用。相反，我们将使用合成的卷曲线圈，并对其进行调整以识别目标蛋白质。此外，对于第二种应用，卷曲的线圈将被进一步修改，以将目标蛋白与细胞的降解途径联系起来。我们的目标是提供对其他人有用的方法和试剂，用于研究生物功能和开发治疗疾病的新药。这项工作必然是跨学科的。因此，我们聚集了一支由计算和实验化学家、生物化学家和细胞生物学家组成的团队来解决它，并与一家生物技术公司合作，以及时和相关的方式翻译工作。

项目成果

Peptide Macrocyclization via Intramolecular Interception of Visible-Light-Mediated Desulfurization

通过分子内拦截可见光介导的脱硫进行肽大环化

• DOI: 10.26434/chemrxiv-2023-865v6
• 发表时间: 2023
• 作者: Smith F

Maleimide constrained BAD BH3 domain peptides as BCL-xL Inhibitors: A versatile approach to rapidly identify sites compatible with peptide constraining

• DOI: 10.1016/j.bmcl.2023.129260
• 发表时间: 2023-04-03
• 期刊: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
• 影响因子: 2.7
• 作者: Zhang，Peiyu;Walko，Martin;Wilson，Andrew J.
• 通讯作者: Wilson，Andrew J.