以 GPCR 为靶标的纳米抗体的生成和表征。

Shenglan Zhang, Zhiran Fan, Jianfeng Liu
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引用次数: 0

摘要

G 蛋白偶联受体(GPCR)是一个庞大的细胞膜蛋白家族,是药物研发的重要目标。纳米抗体(又称 VHH(纯重链抗体的可变域,HcAbs)抗体)是从驼科动物中提取的小型抗体片段,由于其与传统抗体相比的优势,作为靶向 GPCRs 的潜在疗法而备受关注。然而,开发靶向 GPCR 的纳米抗体也面临挑战,其中最重要的挑战是表位的可及性,因为细胞膜会部分屏蔽 GPCR 表面。我们开发了一种通用方案,利用GPCR过表达HEK293细胞的细胞膜提取物作为美洲驼/羊驼免疫抗原,制作靶向GPCR的纳米抗体。我们构建了一个免疫 VHH 库,并通过噬菌体展示生物筛选鉴定了纳米抗体。单克隆纳米抗体在大肠杆菌(E. coli)中重组表达并纯化,以鉴定其结合效力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Generation and characterization of nanobodies targeting GPCR.

G protein-coupled receptors (GPCRs) are a large family of cell membrane proteins that are important targets for drug discovery. Nanobodies, also known as VHH (variable domains of heavy chain-only antibodies, HcAbs) antibodies, are small antibody fragments derived from camelids that have gained significant attention as potential therapeutics for targeting GPCRs due to their advantages over conventional antibodies. However, there are challenges in developing nanobodies targeting GPCRs, among which epitope accessibility is the most significant because the cell membrane partially shields the GPCR surface. We developed a universal protocol for making nanobodies targeting GPCRs using the cell membrane extract of GPCR-overexpressing HEK293 cells as the llama/alpaca immunization antigen. We constructed an immune VHH library and identified nanobodies by phage display bio-panning. The monoclonal nanobodies were recombinantly expressed in Escherichia coli (E. coli) and purified to characterize their binding potency.

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