细胞内抗体和生物降解剂:超越小分子,再回来

IF 4.7 3区 工程技术 Q2 ENGINEERING, BIOMEDICAL
D. Cardella, D. Sanchez-Guzman, T.H. Rabbitts
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引用次数: 0

摘要

在过去的20年里,细胞内抗体作为一种强大的研究工具被用于抑制蛋白质以传递蛋白质功能的特定信息。因此,细胞内抗体已被用于肿瘤学的靶标验证,并且是第一批抑制“不可药物”靶标的试剂,如RAS突变体和LMO2。它们的多功能性允许添加效应功能,以调用细胞内目标接合后的细胞表型。此外,细胞内抗体的旁位-表位相互作用最近被用于开发小分子替代品。我们将讨论细胞内抗体在涉及异常蛋白表达的所有临床适应症(肿瘤、神经系统疾病、感染、炎症)中为发现研究和新一代治疗提供的灵活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intracellular antibodies and biodegraders: Beyond small molecules and back again

Intracellular antibodies have been deployed as powerful research tools for the last 20 years for inhibition of proteins to convey specific information about protein function. Accordingly, intracellular antibodies have been used for target validation in oncology and were the first reagents to inhibit “undruggable” targets, such as RAS mutants and LMO2. Their versatility allows addition of effector functions to invoke cell phenotypes following target engagement inside cells. Moreover, the paratope–epitope interaction of intracellular antibodies has been recently exploited to develop small molecule surrogates. We will discuss the flexibility that intracellular antibodies provide for discovery research and for new generations of therapeutics in all clinical indications where an aberrant protein expression is involved (oncology, neurological disease, infection, inflammation).

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来源期刊
Current Opinion in Biomedical Engineering
Current Opinion in Biomedical Engineering Medicine-Medicine (miscellaneous)
CiteScore
8.60
自引率
2.60%
发文量
59
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