Department of Bioengineering, University of Pennsylvania, Philadelphia, PA, USA.
Interdisciplinary Life Sciences Graduate Programs, The University of Texas at Austin, Austin, TX, USA.
Methods Mol Biol. 2022;2574:183-208. doi: 10.1007/978-1-0716-2712-9_8.
Linking antigen specificity to T cell receptor (TCR) sequences is critical, albeit challenging, to both understanding T cell biology and developing T cell-based therapeutics. Here, we describe in detail tetramer-associated TCR sequencing (TetTCR-Seq), a novel approach to tackling this challenge. TetTCR-Seq is accomplished by multiplexing DNA-barcoded peptide-MHC (pMHC) tetramers, allowing for simultaneous recall of antigen specificity and TCR sequences after single cell sequencing. Additionally, TetTCR-Seq simplifies labor and cuts cost by taking advantage of in vitro transcription and translation (IVTT) to generate peptide libraries and DNA barcodes, in parallel, from the same template. Thus, TetTCR-Seq is a powerful technology capable of quickly and affordably surveying the T cell repertoire for hundreds of antigen specificities in a single experiment.
将抗原特异性与 T 细胞受体 (TCR) 序列联系起来,对于理解 T 细胞生物学和开发基于 T 细胞的治疗方法至关重要,但也极具挑战性。在这里,我们详细描述了 tetramer-associated TCR 测序 (TetTCR-Seq),这是一种解决这一挑战的新方法。TetTCR-Seq 通过多重 DNA 编码肽-MHC(pMHC)四聚体来实现,允许在单细胞测序后同时召回抗原特异性和 TCR 序列。此外,TetTCR-Seq 利用体外转录和翻译 (IVTT) 从同一模板平行生成肽文库和 DNA 条码,从而简化了工作流程并降低了成本。因此,TetTCR-Seq 是一种强大的技术,能够在单个实验中快速、经济地对数百种抗原特异性的 T 细胞库进行调查。