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Targeted Protein Degradation: Advances, Challenges, and Prospects for Computational Methods

泛素连接酶 泛素 计算生物学 小分子 药物发现 三元络合物 对接(动物) 蛋白质降解 药物开发 生化工程 化学 计算机科学 纳米技术 药品 生物 生物化学 材料科学 药理学 工程类 医学 基因 护理部
作者
Barmak Mostofian,Holli‐Joi Martin,Asghar M. Razavi,Shivam Patel,Bryce K. Allen,Woody Sherman,Jesús A. Izaguirre
出处
期刊:Journal of Chemical Information and Modeling [American Chemical Society]
卷期号:63 (17): 5408-5432 被引量:59
标识
DOI:10.1021/acs.jcim.3c00603
摘要

The therapeutic approach of targeted protein degradation (TPD) is gaining momentum due to its potentially superior effects compared with protein inhibition. Recent advancements in the biotech and pharmaceutical sectors have led to the development of compounds that are currently in human trials, with some showing promising clinical results. However, the use of computational tools in TPD is still limited, as it has distinct characteristics compared with traditional computational drug design methods. TPD involves creating a ternary structure (protein-degrader-ligase) responsible for the biological function, such as ubiquitination and subsequent proteasomal degradation, which depends on the spatial orientation of the protein of interest (POI) relative to E2-loaded ubiquitin. Modeling this structure necessitates a unique blend of tools initially developed for small molecules (e.g., docking) and biologics (e.g., protein-protein interaction modeling). Additionally, degrader molecules, particularly heterobifunctional degraders, are generally larger than conventional small molecule drugs, leading to challenges in determining drug-like properties like solubility and permeability. Furthermore, the catalytic nature of TPD makes occupancy-based modeling insufficient. TPD consists of multiple interconnected yet distinct steps, such as POI binding, E3 ligase binding, ternary structure interactions, ubiquitination, and degradation, along with traditional small molecule properties. A comprehensive set of tools is needed to address the dynamic nature of the induced proximity ternary complex and its implications for ubiquitination. In this Perspective, we discuss the current state of computational tools for TPD. We start by describing the series of steps involved in the degradation process and the experimental methods used to characterize them. Then, we delve into a detailed analysis of the computational tools employed in TPD. We also present an integrative approach that has proven successful for degrader design and its impact on project decisions. Finally, we examine the future prospects of computational methods in TPD and the areas with the greatest potential for impact.
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