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通过苯硫代氨基甲酰衍生物分析测定组织材料有机溶剂提取物中的蛋白质、磷脂酰乙醇胺和磷脂酰丝氨酸。

Determination of proteins, phosphatidylethanolamine, and phosphatidylserine in organic solvent extracts of tissue material by analysis of phenylthiocarbamyl derivatives.

作者信息

Stark M, Wang Y, Danielsson O, Jörnvall H, Johansson J

机构信息

Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.

出版信息

Anal Biochem. 1998 Dec 1;265(1):97-102. doi: 10.1006/abio.1998.2856.

Abstract

Amino acid analysis of organic solvent extracts of tissue material has been evaluated for determination of protein content. Conventional ninhydrin-based analysis does not allow determination of a large number of lipid-rich samples. Therefore, the hydrolyzed samples were treated with phenylisothiocyanate and the phenylthiocarbamyl (PTC) derivatives obtained were separated by reverse-phase HPLC. With this method, analysis of many lipid-rich samples is feasible. In addition, phosphatidylethanolamine and phosphatidylserine can then be determined together with the amino acid constituents. The PTC/reverse-phase HPLC method was used for analysis of chloroform/methanol extracts of spinal cord, lung, and bile after chromatography on Lipidex 5000 in methanol/ethylene chloride, 4:1 (v/v). The chromatography profiles show that in all tissue samples the proteins elute before the phospholipids. Consequently, a single step of Lipidex 5000 chromatography can be used to purify polypeptides present in organic solvent extracts. Using pulmonary surfactant extracts (with about 98% phospholipids and 1-2% proteins), we find that individual contents of surfactant proteins B and C can be determined by amino acid analysis.

摘要

已对组织材料的有机溶剂提取物进行氨基酸分析以测定蛋白质含量。传统的基于茚三酮的分析方法无法测定大量富含脂质的样品。因此,将水解后的样品用异硫氰酸苯酯处理,所得的苯硫代氨基甲酰(PTC)衍生物通过反相高效液相色谱法进行分离。采用这种方法,对许多富含脂质的样品进行分析是可行的。此外,磷脂酰乙醇胺和磷脂酰丝氨酸随后可与氨基酸成分一起测定。PTC/反相高效液相色谱法用于分析脊髓、肺和胆汁的氯仿/甲醇提取物,这些提取物先在甲醇/二氯乙烷(4:1,v/v)中于Lipidex 5000上进行色谱分离。色谱图谱表明,在所有组织样品中,蛋白质在磷脂之前洗脱。因此,Lipidex 5000色谱的单个步骤可用于纯化有机溶剂提取物中存在的多肽。使用肺表面活性剂提取物(约含98%的磷脂和1 - 2%的蛋白质),我们发现表面活性剂蛋白B和C的个体含量可通过氨基酸分析来测定。

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