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靶向细胞质膜转运蛋白的治疗性纳米抗体:高风险/高收益的尝试。

Therapeutic Nanobodies Targeting Cell Plasma Membrane Transport Proteins: A High-Risk/High-Gain Endeavor.

机构信息

Department of In Vitro Toxicology and Dermato-Cosmetology, Vrije Universiteit Brussel, Laarbeeklaan 103, 1090 Brussels, Belgium.

Laboratory of Cellular and Molecular Immunology, Vrije Universiteit Brussel, Pleinlaan 2, 1050 Brussels, Belgium.

出版信息

Biomolecules. 2021 Jan 6;11(1):63. doi: 10.3390/biom11010063.

Abstract

Cell plasma membrane proteins are considered as gatekeepers of the cell and play a major role in regulating various processes. Transport proteins constitute a subclass of cell plasma membrane proteins enabling the exchange of molecules and ions between the extracellular environment and the cytosol. A plethora of human pathologies are associated with the altered expression or dysfunction of cell plasma membrane transport proteins, making them interesting therapeutic drug targets. However, the search for therapeutics is challenging, since many drug candidates targeting cell plasma membrane proteins fail in (pre)clinical testing due to inadequate selectivity, specificity, potency or stability. These latter characteristics are met by nanobodies, which potentially renders them eligible therapeutics targeting cell plasma membrane proteins. Therefore, a therapeutic nanobody-based strategy seems a valid approach to target and modulate the activity of cell plasma membrane transport proteins. This review paper focuses on methodologies to generate cell plasma membrane transport protein-targeting nanobodies, and the advantages and pitfalls while generating these small antibody-derivatives, and discusses several therapeutic nanobodies directed towards transmembrane proteins, including channels and pores, adenosine triphosphate-powered pumps and porters.

摘要

细胞浆膜蛋白被认为是细胞的“守门员”,在调节各种过程中起着重要作用。转运蛋白是细胞浆膜蛋白的一个子类,使细胞外环境和细胞质之间的分子和离子交换成为可能。许多人类疾病与细胞浆膜转运蛋白的表达改变或功能障碍有关,这使它们成为有趣的治疗药物靶点。然而,寻找治疗方法具有挑战性,因为许多针对细胞浆膜蛋白的药物候选物由于选择性、特异性、效力或稳定性不足,在(临床前)测试中失败。纳米抗体满足了这些特性,这使得它们有可能成为针对细胞浆膜蛋白的治疗药物。因此,基于治疗性纳米抗体的策略似乎是一种有效的方法,可以靶向和调节细胞浆膜转运蛋白的活性。本文重点介绍了针对细胞浆膜转运蛋白的纳米抗体的生成方法,以及在生成这些小分子抗体衍生物时的优势和缺陷,并讨论了几种针对跨膜蛋白(包括通道和孔、三磷酸腺苷驱动泵和转运体)的治疗性纳米抗体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9af/7825061/e3109f503318/biomolecules-11-00063-g001.jpg

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