Spillane Katelyn M, Tolar Pavel
Immune Receptor Activation Laboratory, The Francis Crick Institute, 1 Midland Road, London, NW1 1AT, UK.
Division of Immunology and Inflammation, Department of Medicine, Imperial College London, London, UK.
Methods Mol Biol. 2018;1707:69-80. doi: 10.1007/978-1-4939-7474-0_5.
The production of antibodies requires the expansion and selection of high-affinity B cell clones. This process is initiated by antigen uptake through the B cell receptor (BCR), which recognizes and binds antigen displayed on the surface of an antigen-presenting cell (APC). To acquire the antigen, B cells use myosin contractility to physically pull BCR-antigen clusters from the APC membrane. These mechanical forces influence association and dissociation rates of BCR-antigen bonds, resulting in affinity-dependent acquisition of antigen by B cells. Mechanical regulation of B cell antigen acquisition from APCs remains poorly understood, although the recent development of DNA-based force sensors has enabled the measurement of mechanical forces generated in B cell-APC contacts. In this chapter, we describe a protocol to design, synthesize, and purify DNA-based force sensors to measure B cell antigen extraction forces using fluorescence microscopy.
抗体的产生需要高亲和力B细胞克隆的扩增和选择。这个过程由通过B细胞受体(BCR)摄取抗原启动,BCR识别并结合抗原呈递细胞(APC)表面展示的抗原。为了获取抗原,B细胞利用肌球蛋白收缩力从APC膜上物理性地拉拽BCR-抗原簇。这些机械力影响BCR-抗原键的结合和解离速率,导致B细胞以亲和力依赖的方式获取抗原。尽管基于DNA的力传感器的最新发展使得测量B细胞与APC接触时产生的机械力成为可能,但对B细胞从APC获取抗原的机械调节仍知之甚少。在本章中,我们描述了一种设计、合成和纯化基于DNA的力传感器以使用荧光显微镜测量B细胞抗原提取力的方案。