Rabbitts T H
Institute of Cancer Research, Division of Cancer Therapeutics, 15 Cotswold Road, Sutton, London SM2 5NG, UK.
Antibodies (Basel). 2023 Mar 16;12(1):24. doi: 10.3390/antib12010024.
The application of antibodies in cells was first shown in the early 1990s, and subsequently, the field of intracellular antibodies has expanded to encompass antibody fragments and their use in target validation and as engineered molecules that can be fused to moieties (referred to as warheads) to replace the Fc effector region of a whole immunoglobulin to elicit intracellular responses, such as cell death pathways or protein degradation. These various forms of intracellular antibodies have largely been used as research tools to investigate function within cells by perturbing protein activity. New applications of such molecules are on the horizon, namely their use as drugs and as templates for small-molecule drug discovery. The former is a potential new pharmacology that could harness the power and flexibility of molecular biology to generate new classes of drugs (herein referred to as macrodrugs when used in the context of disease control). Delivery of engineered intracellular antibodies, and other antigen-binding macromolecules formats, into cells to produce a therapeutic effect could be applied to any therapeutic area where regulation, degradation or other kinds of manipulation of target proteins can produce a therapeutic effect. Further, employing single-domain antibody fragments as competitors in small-molecule screening has been shown to enable identification of drug hits from diverse chemical libraries. Compounds selected in this way can mimic the effects of the intracellular antibodies that have been used for target validation. The capability of intracellular antibodies to discriminate between closely related proteins lends a new dimension to drug screening and drug development.
抗体在细胞中的应用最早于20世纪90年代初得到证实,随后,细胞内抗体领域不断扩展,涵盖了抗体片段及其在靶点验证中的应用,以及作为可与部分(称为弹头)融合的工程化分子,以取代完整免疫球蛋白的Fc效应区域,从而引发细胞内反应,如细胞死亡途径或蛋白质降解。这些不同形式的细胞内抗体在很大程度上已被用作研究工具,通过干扰蛋白质活性来研究细胞内的功能。此类分子的新应用即将出现,即用作药物以及小分子药物发现的模板。前者是一种潜在的新药理学,它可以利用分子生物学的力量和灵活性来产生新的药物类别(在疾病控制的背景下使用时,本文称为大分子药物)。将工程化细胞内抗体和其他抗原结合大分子形式递送至细胞中以产生治疗效果,可应用于任何通过调节、降解或其他方式操纵靶蛋白能产生治疗效果的治疗领域。此外,已证明在小分子筛选中使用单域抗体片段作为竞争剂能够从不同的化学文库中鉴定出药物先导物。以这种方式选择的化合物可以模拟用于靶点验证的细胞内抗体的作用。细胞内抗体区分密切相关蛋白质的能力为药物筛选和药物开发带来了新的维度。