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人类免疫球蛋白Vλ基因片段的克隆与测序

Cloning and sequencing of human immunoglobulin V lambda gene segments.

作者信息

Williams S C, Winter G

机构信息

MRC Laboratory of Molecular Biology, Cambridge.

出版信息

Eur J Immunol. 1993 Jul;23(7):1456-61. doi: 10.1002/eji.1830230709.

Abstract

To provide the building blocks for making synthetic antibody fragments we have used the polymerase chain reaction (PCR) to clone human variable (V) gene segments of lambda light chains. The PCR primers were based on the sequences of known human V lambda segments, and were used to isolate 14 new V lambda segments (including 4 pseudogenes) from a single individual. We have compiled a sequence directory from this data and other sources to include all known human V lambda segments with open reading frames and we have identified a new V lambda family (V lambda IX). Almost all of the segments (22/24) have different sequences in the complementarity-determining regions, setting a lower limit to the structural diversity of the antigen binding sites encoded by human V lambda genes in the human population.

摘要

为了提供合成抗体片段的构建模块,我们利用聚合酶链反应(PCR)克隆了λ轻链的人类可变(V)基因片段。PCR引物基于已知人类Vλ片段的序列,用于从单个个体中分离出14个新的Vλ片段(包括4个假基因)。我们根据这些数据和其他来源编制了一个序列目录,以纳入所有具有开放阅读框的已知人类Vλ片段,并且我们鉴定出了一个新的Vλ家族(VλIX)。几乎所有片段(22/24)在互补决定区都有不同的序列,这为人类群体中人类Vλ基因编码的抗原结合位点的结构多样性设定了下限。

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