分享

( 请教)关于免疫球蛋白轻重链的分型依据

 qqkingdom 2014-03-10
                                                      办事情总得有始有终,给老外写信得到的答复,相信这个对大家比较有用吧,拿出来跟大家分享了,呵呵:
there is no real major sequence difference between kappa and lambda;
the sequence differences are quite subtle. You can usually tell which
a sequence is by looking at CDR-L1. In kappa, CDR-L1 generally starts
with a sequence like RAS, QAS, RTS, RMS, KSS, RST, SAS. In other words,
L24 is normally R or K, sometimes Q or S
L25 is normally A, sometimes T, M or S
L26 is normally S, occasionally T

On the other hand, lambda sequences tend to be SGD, SGG, SGS, GGN, GNN,
TGT, TLR, TLS. In other words,
L24 is normally S, G or T
L25 is normally G, sometimes L
L26 is normally D,G,N,S,R or T

Also in Kappa, L47 is almost always W or L
in Lambda, L47 is I, L, V or M

I could go on describing more trends like these, but basically, as with
the human heavy chain sub-classes, you have to build up a set of
propensities for each residue at each position for lambda and kappa and
score your sequence against those profiles to see which it matches better.                                                    

    本站是提供个人知识管理的网络存储空间,所有内容均由用户发布,不代表本站观点。请注意甄别内容中的联系方式、诱导购买等信息,谨防诈骗。如发现有害或侵权内容,请点击一键举报。
    转藏 分享 献花(0

    0条评论

    发表

    请遵守用户 评论公约