Apley Kyle D, Griffin J Daniel, Johnson Stephanie N, Berkland Cory J, DeKosky Brandon J
Department of Pharmaceutical Chemistry, University of Kansas.
Department of Pharmaceutical Chemistry, University of Kansas; Bioengineering Graduate Program, University of Kansas; Department of Chemical and Petroleum Engineering, University of Kansas.
J Vis Exp. 2020 Oct 20(164). doi: 10.3791/61827.
Fluorescent antigen production is a critical step in the identification of antigen-specific B cells. Here, we detailed the preparation, purification, and the use of four-arm, fluorescent PEG-antigen conjugates to selectively identify antigen-specific B cells through avid engagement with cognate B cell receptors. Using modular click chemistry and commercially available fluorophore kit chemistries, we demonstrated the versatility of preparing customized fluorescent PEG-conjugates by creating distinct arrays for proteolipid protein (PLP139-151) and insulin, which are important autoantigens in murine models of multiple sclerosis and type 1 diabetes, respectively. Assays were developed for each fluorescent conjugate in its respective disease model using flow cytometry. Antigen arrays were compared to monovalent autoantigen to quantify the benefit of multimerization onto PEG backbones. Finally, we illustrated the utility of this platform by isolating and assessing anti-insulin B cell responses after antigen stimulation ex vivo. Labeling insulin-specific B cells enabled the amplified detection of changes to co-stimulation (CD86) that were otherwise dampened in aggregate B cell analysis. Together, this report enables the production and use of fluorescent antigen arrays as a robust tool for probing B cell populations.
荧光抗原的制备是鉴定抗原特异性B细胞的关键步骤。在此,我们详细介绍了四臂荧光聚乙二醇-抗原偶联物的制备、纯化及应用,通过与同源B细胞受体的强力结合来选择性鉴定抗原特异性B细胞。利用模块化的点击化学和市售荧光团试剂盒化学方法,我们展示了通过为蛋白脂蛋白(PLP139 - 151)和胰岛素创建不同阵列来制备定制荧光聚乙二醇偶联物的多功能性,它们分别是多发性硬化症和1型糖尿病小鼠模型中的重要自身抗原。在各自的疾病模型中,利用流式细胞术为每种荧光偶联物开发了检测方法。将抗原阵列与单价自身抗原进行比较,以量化在聚乙二醇主链上进行多聚化的益处。最后,我们通过体外分离和评估抗原刺激后的抗胰岛素B细胞反应,说明了该平台的实用性。标记胰岛素特异性B细胞能够放大检测共刺激(CD86)的变化,而这些变化在总体B细胞分析中会被抑制。总之,本报告实现了荧光抗原阵列的制备和应用,作为探测B细胞群体的强大工具。