肿瘤免疫微环境中蛋白-蛋白相互作用组的定位

Q2 Medicine Antibody Therapeutics Pub Date : 2023-11-14 DOI:10.1093/abt/tbad026
Rui Peng, Mi Deng
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引用次数: 0

摘要

细胞间的通讯主要通过细胞表面和分泌蛋白进行,它们形成一个复杂的网络,协调全身免疫功能。揭示这些蛋白-蛋白相互作用(PPIs)对于理解分子机制和阐明疾病下的免疫系统异常是必不可少的。由于常用技术的通量相对较低,传统的生物学研究通常集中在有限数量的PPI对上。令人鼓舞的是,经典方法已经取得了进步,许多适合大规模蛋白质-蛋白质筛选的新系统已经开发出来并成功使用。这些高通量PPI研究技术已经在绘制免疫细胞相互作用组、丰富PPI数据库和分析工具、发现癌症和其他疾病的治疗靶点等方面取得了相当大的成就,必将为这一领域带来前所未有的见解。
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Mapping the protein-protein interactome in the tumor immune microenvironment
Abstract The cell-to-cell communication primarily occurs through cell-surface and secreted proteins, which form a sophisticated network that coordinates systemic immune function. Uncovering these protein-protein interactions (PPIs) is indispensable for understanding the molecular mechanism and elucidating immune system aberrances under diseases. Traditional biological studies typically focus on a limited number of PPI pairs due to the relative low throughput of commonly used techniques. Encouragingly, classical methods have advanced, and many new systems tailored for large-scale protein-protein screening have been developed and successfully utilized. These high-throughput PPI investigation techniques have already made considerable achievements in mapping the immune cell interactome, enriching PPI databases and analysis tools, and discovering therapeutic targets for cancer and other diseases, which will definitely bring unprecedented insight into this field.
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来源期刊
Antibody Therapeutics
Antibody Therapeutics Medicine-Immunology and Allergy
CiteScore
8.70
自引率
0.00%
发文量
30
审稿时长
8 weeks
期刊最新文献
AI-based antibody discovery platform identifies novel, diverse, and pharmacologically active therapeutic antibodies against multiple SARS-CoV-2 strains. FcRider: a recombinant Fc nanoparticle with endogenous adjuvant activities for hybrid immunization. A pan-allelic human SIRPα-blocking antibody, ES004-B5, promotes tumor killing by enhancing macrophage phagocytosis and subsequently inducing an effective T-cell response. Correction to: A case study of a bispecific antibody manufacturability assessment and optimization during discovery stage and its implications. The process using a synthetic library that generates multiple diverse human single domain antibodies.
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