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编码人补体因子H C末端的cDNA克隆的序列分析

Sequence analysis of a cDNA clone encoding the C-terminal end of human complement factor H.

作者信息

Day A J, Ripoche J, Lyons A, McIntosh B, Harris T J, Sim R B

机构信息

Department of Biochemistry, University of Oxford, UK.

出版信息

Biosci Rep. 1987 Mar;7(3):201-7. doi: 10.1007/BF01124790.

Abstract

Peptide sequencing of the complement system regulatory protein, factor H, permitted the synthesis of a mixed sequence oligonucleotide probe. Human liver cDNA libraries were screened and factor H-specific clones selected. No full-length clone was obtained, but the largest available clone, R2a, was found to encode the C-terminal 657 amino acids of factor H. The derived amino acid sequence consists of 10 contiguous internally homologous segments, each about 60 amino acids long. Sequences homologous to these are found in several other complement and non-complement proteins. Such sequences are likely to represent a particular type of tertiary structure subunit.

摘要

对补体系统调节蛋白H因子进行肽测序,从而合成了混合序列寡核苷酸探针。对人肝脏cDNA文库进行筛选,并挑选出H因子特异性克隆。未获得全长克隆,但发现最大的可用克隆R2a编码H因子的C端657个氨基酸。推导的氨基酸序列由10个连续的内部同源片段组成,每个片段约60个氨基酸长。在其他几种补体和非补体蛋白中也发现了与这些序列同源的序列。这些序列可能代表一种特殊类型的三级结构亚基。

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