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生物样品中同型半胱氨酸硫内酯的测定。

The determination of homocysteine-thiolactone in biological samples.

作者信息

Jakubowski Hieronim

机构信息

Department of Microbiology and Molecular Genetics, UMDNJ-New Jersey Medical School, International Center for Public Health, Newark 07101, USA.

出版信息

Anal Biochem. 2002 Sep 1;308(1):112-9. doi: 10.1016/s0003-2697(02)00224-5.

Abstract

Homocysteine-thiolactone, a cyclic thioester of homocysteine, is synthesized by methionyl-tRNA synthetase in all cell types. A new assay for the determination of homocysteine-thiolactone in biological samples is described. The assay involves separation of homocysteine-thiolactone from macromolecules by ultrafiltration. Homocysteine-thiolactone is further purified and quantified by high-pressure liquid chromatography either on a reverse phase or a cation exchange micro-bore column. The detection and quantitation are obtained by monitoring the absorbance at 240 nm, a maximum in a UV spectrum of homocysteine-thiolactone. The sensitivity of detection is 5 pmol. This assay has been applied to bacteria (Escherichia coli and Mycobacterium smegmatis), the yeast Saccharomyces cerevisiae, cultured human vascular endothelial cells, and human plasma. The data support the conclusion that homocysteine-thiolactone is a ubiquitous metabolite whose levels are directly related to homocysteine levels.

摘要

同型半胱氨酸硫内酯是同型半胱氨酸的一种环状硫酯,在所有细胞类型中由甲硫氨酰 - tRNA合成酶合成。本文描述了一种测定生物样品中同型半胱氨酸硫内酯的新方法。该方法包括通过超滤将同型半胱氨酸硫内酯与大分子分离。同型半胱氨酸硫内酯进一步通过反相或阳离子交换微径柱上的高压液相色谱法进行纯化和定量。通过监测240nm处的吸光度进行检测和定量,这是同型半胱氨酸硫内酯紫外光谱中的最大值。检测灵敏度为5皮摩尔。该方法已应用于细菌(大肠杆菌和耻垢分枝杆菌)、酿酒酵母、培养的人血管内皮细胞和人血浆。数据支持以下结论:同型半胱氨酸硫内酯是一种普遍存在的代谢物,其水平与同型半胱氨酸水平直接相关。

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