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体外将硫酸根离子掺入突触膜糖蛋白中。

The incorporation in vitro of sulphate ions into synaptic-membrane glycoproteins.

作者信息

White C J

出版信息

Biochem J. 1981 Nov 15;200(2):373-7. doi: 10.1042/bj2000373.

Abstract

Synaptosomes from sheep brain cortex were incubated with carrier-free Na235SO4 and the synaptic plasma membranes were isolated. The membranes were free of contamination from cytosol, mitochondria and microsomal material and accounted for 30% of the radioactivity present in the synaptosomal particulate fraction. Control experiments demonstrated that the radioactivity present in the preparation was not due to non-specific binding of sulphate ions. The synaptic membranes contained at least six 35S-containing protein bands with molecular weights between 160 000 and 16 000. Analysis showed that the radioactivity was located in the carbohydrate moiety of a glycopeptide.

摘要

将来自绵羊大脑皮层的突触体与无载体的Na235SO4一起孵育,然后分离突触质膜。这些膜没有受到胞质溶胶、线粒体和微粒体物质的污染,占突触体颗粒部分中放射性的30%。对照实验表明,制剂中存在的放射性不是由于硫酸根离子的非特异性结合。突触膜含有至少六条含35S的蛋白带,分子量在160000至16000之间。分析表明,放射性位于一种糖肽的碳水化合物部分。

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Sulphated glycoproteins in synaptosomes.
Neurosci Lett. 1980 Mar;16(3):307-11. doi: 10.1016/0304-3940(80)90016-6.
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Enzyme-linked immunoadsorbent assays for myelin basic protein and antibodies to myelin basic protein.
J Neurochem. 1980 Dec;35(6):1409-17. doi: 10.1111/j.1471-4159.1980.tb09017.x.
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Glycopeptides from rat brain glycoproteins.来自大鼠脑糖蛋白的糖肽。
Biochim Biophys Acta. 1973 May 28;304(3):781-96. doi: 10.1016/0304-4165(73)90225-0.

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