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人红细胞膜唾液酸糖蛋白α和δ的cDNA克隆的分离

Isolation of cDNA clones for human erythrocyte membrane sialoglycoproteins alpha and delta.

作者信息

Tate C G, Tanner M J

机构信息

Department of Biochemistry, University of Bristol, U.K.

出版信息

Biochem J. 1988 Sep 15;254(3):743-50. doi: 10.1042/bj2540743.

Abstract

We have isolated almost full-length cDNA clones corresponding to human erythrocyte membrane sialoglycoproteins alpha (glycophorin A) and delta (glycophorin B). The predicted amino acid sequence of delta differs at two amino acid residues from the sequence determined by peptide sequencing. The sialoglycoprotein delta clone we have isolated contains an interrupting sequence within the region that gives rise to the cleaved N-terminal leader sequence for the protein and represents a product that is unlikely to be inserted into the erythrocyte membrane. Comparison of the cDNA sequences of alpha and delta shows very strong homology at the DNA level within the coding regions. The two mRNA sequences are closely related and differ by a number of clearly defined insertions and deletions.

摘要

我们已经分离出了几乎全长的互补DNA(cDNA)克隆,它们分别对应于人红细胞膜唾液酸糖蛋白α(血型糖蛋白A)和δ(血型糖蛋白B)。δ的预测氨基酸序列与通过肽测序确定的序列在两个氨基酸残基处不同。我们分离出的唾液酸糖蛋白δ克隆在产生该蛋白质裂解N端前导序列的区域内含有一个中断序列,代表一种不太可能插入红细胞膜的产物。α和δ的cDNA序列比较显示,在编码区域内的DNA水平上具有非常强的同源性。这两个信使核糖核酸(mRNA)序列密切相关,并且存在一些明确界定的插入和缺失差异。

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