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用于整合膜蛋白的构象特异性单克隆抗体的产生

Generation of Conformation-Specific Monoclonal Antibodies for Integral Membrane Proteins.

作者信息

Sheldon Natalie, Dhandapani Gunasekaran, Kim Junhoe, Spangler Cathy J, Fang Chengli, Park Jumi, Rao Prashant, Gouaux Eric

机构信息

Vollum Institute, Oregon Health & Science University, Portland, Oregon.

Howard Hughes Medical Institute, Oregon Health & Science University, Portland, Oregon.

出版信息

Curr Protoc. 2025 May;5(5):e70142. doi: 10.1002/cpz1.70142.

Abstract

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.

摘要

抗体及其抗原结合片段,包括抗原结合片段(Fabs)和单链可变片段(scFvs),是生物学各个领域的非凡工具,尤其在神经科学领域,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,构象特异性抗体与三维表位结合,识别靶抗原的天然构象,并且已被证明在X射线晶体学中作为结晶伴侣以及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,它们通常具有极高的特异性,可用于免疫荧光研究以及从天然组织中分离抗原。在过去十年中,我们团队致力于开发针对重要突触受体的鼠单克隆抗体(mAbs),特别是离子型谷氨酸受体(iGluRs)及其辅助蛋白。我们已经开发出可重复的方法来生成用于结构、生化和成像研究的高质量单克隆抗体。在本文中,我们展示了如何制备蛋白脂质体(PLs)、进行免疫并跟踪免疫反应、进行杂交瘤生成,以及通过酶联免疫吸附测定和荧光检测尺寸排阻色谱分析单克隆抗体结合的特异性、交叉反应性和竞争性。我们基于PL的方法在4个月内产生针对多种突触膜受体的高亲和力、构象特异性抗体。在这里,我们详细描述相关方案,并记录我们针对iGluRs及其辅助亚基产生的单克隆抗体、Fabs和scFvs。© 2025作者。由Wiley Periodicals LLC出版的《当前方案》。基本方案1:针对整合膜蛋白生成构象特异性抗体 支持方案1:使用ELISA检测构象抗体 基本方案2:单克隆抗体及其衍生物的表达和纯化 支持方案2:用于Fab纯化的昆虫细胞上清液的浓缩和澄清 支持方案3:使用Octet BLI系统测量离子型谷氨酸受体结合动力学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8449/12105683/e03f92bcb102/CPZ1-5-0-g003.jpg

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