MEASURING CDR3 LENGTH VARIABILITY IN INDIVIDUALS DURING ONTOGENY
MEASURING CDR3 LENGTH VARIABILITY IN INDIVIDUALS DURING ONTOGENY
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DOI：
10.1016/0022-1759(94)90058-2
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发表时间：
1994-02-10
影响因子：
2.2
通讯作者：
HSU, E
中科院分区：
文献类型：
--
作者：
DESRAVINES, S;HSU, E
The portion of the antibody sequence that contributes most to the conformation of the antigen-combining site is the third complementarity-determining region (CDR3). The CDR3 in antibody heavy chains are somatically produced by the rearrangement of three different immunoglobulin (Ig) gene segments, V-H, D and J(H), and are therefore highly variable in sequence and length. We have devised a technique for rapid analysis of CDR3 length variability from a large number of cDNA samples. This technique allows comparative evaluation of IgH heterogeneity in individuals without recourse to DNA cloning and sequencing. We also present data on Ig sequences from different stages of development in the amphibian, Xenopus laevis. Most of the larval and post-metamorphic Ig samples contained CDR3 of 3-10 codons, two codons shorter than those of the adult CDR3, which were 5-12 codons. Antibodies made by immunized tadpoles have been shown to be much less diverse than those produced by adults to the same antigen. The shorter tadpole CDR3 perhaps generates a more limited spectrum of antigen-combining site structures and, in this way, makes for a more restricted antibody repertoire.
