Pannetier C, Cochet M, Darche S, Casrouge A, Zöller M, Kourilsky P
Unité de Biologie Moléculaire du Gène, Institut National de la Santé et de la Recherche Medicale, Institut Pasteur.
Proc Natl Acad Sci U S A. 1993 May 1;90(9):4319-23. doi: 10.1073/pnas.90.9.4319.
A method using PCR amplification and primer extension with fluorescent oligonucleotides was developed to analyze T-cell repertoires. The sizes of the hypervariable CDR3-like regions of the murine T-cell antigen receptor beta chains were measured for all possible V beta-J beta combinations. This analysis shows that beta chains are distributed into at least 2000 groups, a value that provides a lower limit to their complexity. The CDR3 sizes appear to be dependent on the J beta and especially the V beta segment used and correlates with amino acid sequence motifs in the corresponding CDR1 region. This feature of T-cell receptors is discussed.
开发了一种利用聚合酶链反应(PCR)扩增和荧光寡核苷酸引物延伸来分析T细胞库的方法。针对所有可能的Vβ-Jβ组合,测量了小鼠T细胞抗原受体β链高变CDR3样区域的大小。该分析表明,β链至少分布在2000个组中,这一数值为其复杂性提供了下限。CDR3的大小似乎取决于所使用的Jβ,尤其是Vβ片段,并且与相应CDR1区域中的氨基酸序列基序相关。对T细胞受体的这一特性进行了讨论。