The value of coimmunoprecipitation (Co-IP) assays in drug discovery

免疫沉淀 药物发现 药品 计算生物学 化学 生物 药理学 生物化学 基因
作者
Zhongtian Cai,Danni Wang,Zekun Li,M. Gu,Qidong You,Lei Wang
出处
期刊:Expert Opinion on Drug Discovery [Taylor & Francis]
卷期号:20 (7): 859-872 被引量:5
标识
DOI:10.1080/17460441.2025.2497913
摘要

INTRODUCTION: Co-IP assays are well-established technologies widely applicated for investigating the mechanisms underlying protein-protein interactions and identifying protein-protein interaction modulators. These assays play an important role in elucidating the complex networks of protein interactions critical for cellular functions. AREAS COVERED: This review covers a technical protocol of standard Co-IP. The research contents and conclusions of Co-IP in protein-protein interactions and protein-protein interaction modulators are summarized. Finally, three derivations of Co-IP assays are introduced. Literature was surveyed from original publications, standard sources, PubMed and clinical trials through 14 April 2025. EXPERT OPINION: To perform Co-IP successfully, researchers must consider the selection of specific antibody, remission of nonspecific binding and detection limitations for transient or weak interactions. Co-IP assays offer several advantages over tandem affinity purification and pull-down methods, particularly in their applicability to primary cells. This allows for the study of PPIs in a natural cellular environment. Conventional Co-IP assays often struggle to detect weak or transient interactions and can suffer from nonspecific binding contamination. However, advancements in Co-IP techniques address these challenges, enhancing sensitivity and specificity, and enabling the detection of subtle interactions while distinguishing specific binding events. This makes Co-IP a powerful tool for exploring the dynamics of protein interactions in living systems.
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