Molecular Degraders: A Comprehensive Review of Small Molecule Induced Protein Degradation Strategies.

IF 1.9 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Deepanshu Sindhwani, Kaushal Arora, Pankaj Kumar, Prabhakar Kumar Verma, Vivek V Bhosale
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引用次数: 0

Abstract

Molecular degraders represent a ground-breaking class of small molecules revolutionizing drug discovery through the selective elimination of disease-causing proteins, including those previously deemed "undruggable." This review provides a critical analysis of the design and mechanistic intricacies of molecular degraders, encompassing PROTACs, molecular glues, and SNIPERs, with a focus on their reliance on ubiquitin-mediated protein degradation pathways. Key themes include advancements in E3 ligase selection, the principles guiding ternary complex formation, and the role of structural dynamics in optimizing degrader activity and selectivity. The data for this review was collected from various databases such as Science Direct, United States National Library of Medicine (Pubmed), Google Scholar, Elsevier, Springer, and Bentham. Novel findings, such as the development of non-canonical degrader approaches and their preclinical successes, are examined alongside therapeutic applications in oncology, neurodegenerative diseases, and infectious disorders. Challenges, including resistance mechanisms, safety concerns, and pharmacokinetic limitations, are evaluated to provide a holistic perspective. This review not only highlights the transformative potential of molecular degraders but also identifies future directions and critical gaps that could drive innovation in targeted protein degradation and precision medicine.

分子降解:小分子诱导蛋白质降解策略的综合综述。
分子降解剂代表了一类突破性的小分子,通过选择性地消除致病蛋白质,包括那些以前被认为是“不可药物”的蛋白质,彻底改变了药物的发现。这篇综述对分子降解物的设计和机制复杂性进行了批判性分析,包括PROTACs、分子胶和SNIPERs,重点关注它们对泛素介导的蛋白质降解途径的依赖。关键主题包括E3连接酶选择的进展,三元络合物形成的指导原则,以及结构动力学在优化降解酶活性和选择性中的作用。本综述的数据来自不同的数据库,如Science Direct、美国国家医学图书馆(Pubmed)、谷歌Scholar、Elsevier、施普林格和Bentham。新发现,如非规范降解方法的发展及其临床前成功,将与肿瘤、神经退行性疾病和感染性疾病的治疗应用一起进行检查。挑战,包括耐药机制,安全性问题和药代动力学限制,进行评估,以提供一个整体的观点。这篇综述不仅强调了分子降解物的变革潜力,而且确定了未来的方向和关键空白,可以推动靶向蛋白质降解和精准医学的创新。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Current protein & peptide science
Current protein & peptide science 生物-生化与分子生物学
CiteScore
5.20
自引率
0.00%
发文量
73
审稿时长
6 months
期刊介绍: Current Protein & Peptide Science publishes full-length/mini review articles on specific aspects involving proteins, peptides, and interactions between the enzymes, the binding interactions of hormones and their receptors; the properties of transcription factors and other molecules that regulate gene expression; the reactions leading to the immune response; the process of signal transduction; the structure and function of proteins involved in the cytoskeleton and molecular motors; the properties of membrane channels and transporters; and the generation and storage of metabolic energy. In addition, reviews of experimental studies of protein folding and design are given special emphasis. Manuscripts submitted to Current Protein and Peptide Science should cover a field by discussing research from the leading laboratories in a field and should pose questions for future studies. Original papers, research articles and letter articles/short communications are not considered for publication in Current Protein & Peptide Science.
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