完整膜蛋白构象特异性单克隆抗体的制备

IF 2.2
Natalie Sheldon, Gunasekaran Dhandapani, Junhoe Kim, Cathy J. Spangler, Chengli Fang, Jumi Park, Prashant Rao, Eric Gouaux
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引用次数: 0

摘要

抗体及其抗原结合片段,包括片段抗原结合域(fab)和单链可变片段(scFvs),是生物学所有领域的非凡工具,特别是在神经科学领域,它们已被用于成像、检测和定量研究。大多数抗体与非结构化或线性表位结合。相比之下,构象特异性抗体与3D表位结合,识别靶抗原的天然构象,并已被证明在x射线晶体学中作为结晶伴侣和在冷冻电子显微镜中作为基准标记非常有用。此外,由于构象特异性抗体识别抗原的三维形状,它们通常具有精细的特异性,在免疫荧光研究和从天然组织中分离抗原时很有用。在过去的十年中,我们的团队致力于开发针对重要突触受体的小鼠单克隆抗体(mab),特别是嗜离子性谷氨酸受体(iGluRs)及其辅助蛋白。我们已经开发出可重复的方法来生成高质量的单克隆抗体,用于结构、生化和成像研究。在本文中,我们展示了如何制备蛋白脂质体(PLs),进行免疫和跟踪免疫反应,进行杂交瘤的产生,并通过酶联免疫吸附试验和荧光检测大小排斥层析分析单抗结合的特异性,交叉反应性和竞争。我们基于pl的方法在4个月内产生针对不同突触膜受体的高亲和力,构象特异性抗体。在这里,我们详细描述了相关的协议,并记录了我们针对iGluRs及其辅助亚基产生的单克隆抗体、单克隆抗体和单克隆抗体。©2025作者。Wiley期刊有限责任公司发表的当前协议。基本协议1:生成完整膜蛋白构象特异性抗体支持协议1:使用elisa检测构象抗体基本协议2:单克隆抗体及其衍生物的表达和纯化支持协议2:用于Fab纯化的昆虫细胞上清的浓度和澄清支持协议3:用Octet BLI系统测量嗜离子性谷氨酸受体结合动力学
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Generation of Conformation-Specific Monoclonal Antibodies for Integral Membrane Proteins

Generation of Conformation-Specific Monoclonal Antibodies for Integral Membrane Proteins

Generation of Conformation-Specific Monoclonal Antibodies for Integral Membrane Proteins

Generation of Conformation-Specific Monoclonal Antibodies for Integral Membrane Proteins

Generation of Conformation-Specific Monoclonal Antibodies for Integral Membrane Proteins

Antibodies and their antigen-binding fragments, including fragment antigen-binding domains (Fabs) and single-chain variable fragments (scFvs), are extraordinary tools in all fields of biology, particularly in neuroscience, where they have been utilized for imaging, detection, and quantification studies. Most antibodies bind to unstructured or linear epitopes. Conformation-specific antibodies, by contrast, bind to 3D epitopes, recognizing native conformations of the target antigen, and have proven highly useful in X-ray crystallography as crystallization chaperones and in cryo-electron microscopy as fiducial markers. Moreover, because conformation-specific antibodies recognize 3D shapes of the antigen, they often have exquisite specificity and are useful in immunofluorescence studies and in isolation of antigen from native tissues. Over the past decade, our group has devoted effort to developing murine monoclonal antibodies (mAbs) against important synaptic receptors, particularly ionotropic glutamate receptors (iGluRs) and their auxiliary proteins. We have developed reproducible methods for generating high-quality mAbs for structural, biochemical, and imaging studies. In this article, we show how to prepare proteoliposomes (PLs), carry out immunization and track the immune response, perform hybridoma generation, and analyze the specificity, cross-reactivity, and competition of mAb binding via enzyme-linked immunosorbent assay and fluorescence-detection size-exclusion chromatography. Our PL-based method produces high-affinity, conformation-specific antibodies targeting diverse synaptic membrane receptors in 4 months. Here, we describe the relevant protocols in detail and document the mAbs, Fabs, and scFvs that we have produced against iGluRs and their auxiliary subunits. © 2025 The Author(s). Current Protocols published by Wiley Periodicals LLC.

Basic Protocol 1: Generation of conformation-specific antibodies for integral membrane proteins

Support Protocol 1: Detection of conformational antibodies using ELISA

Basic Protocol 2: Expression and purification of monoclonal antibodies and their derivatives

Support Protocol 2: Concentration and clarification of insect cell supernatant for Fab purification

Support Protocol 3: Measurement of ionotropic glutamate receptor binding kinetics using Octet BLI System

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