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人前列腺组织中一种脂肪酸结合蛋白的纯化与特性分析

Purification and characterization of a fatty acid binding protein from human prostatic tissue.

作者信息

Chaudry A A, Dutta-Roy A K

机构信息

Department of Urology, Aberdeen Royal Infirmary, Scotland, United Kingdom.

出版信息

Lipids. 1993 May;28(5):383-8. doi: 10.1007/BF02535934.

Abstract

Epidemiological studies suggest the existence of a strong relationship between the incidence of prostatic cancer and the intake of dietary lipids in humans. However, very little information is available on intracellular fatty acid metabolism in human prostatic tissue. The objective of this study was to identify and subsequently characterize a fatty acid binding protein of human prostatic tissue. A fatty acid binding protein (FABP) was purified and characterized from human prostatic tissue. The purified FABP had an apparent molecular mass of 15.0 +/- 1.0 kDa as averaged from three different methods, sodium dodecylsulfate-polyacrylamide gel electrophoresis (SDS-PAGE), gel filtration and amino acid analysis. The pI value of the protein was determined to be 6.8. Scatchard analysis of fatty acid binding to the purified FABP from malignant prostatic tissue showed a Kd value of 0.53 +/- 0.02 microM for arachidonic acid (n = 5). The Kd values of FABP purified from benign prostatic tissue were 0.57 +/- 0.02 microM for oleic acid and 0.51 +/- 0.04 microM for arachidonic acid (n = 5). Fatty acid analysis revealed that the level of endogenously bound arachidonic acid was about 2.5-fold higher in FABP from malignant than from benign tissue. In addition, both malignant and benign tissues contained the same concentration of FABP. The concentrations of FABP in malignant and benign tissues were 19.2 +/- 1.8 and 21.4 +/- 2.1 micrograms per mg of total cytosolic protein, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

流行病学研究表明,人类前列腺癌的发病率与膳食脂质的摄入量之间存在密切关系。然而,关于人类前列腺组织中细胞内脂肪酸代谢的信息却非常少。本研究的目的是鉴定并随后表征人类前列腺组织中的一种脂肪酸结合蛋白。从人类前列腺组织中纯化并表征了一种脂肪酸结合蛋白(FABP)。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)、凝胶过滤和氨基酸分析这三种不同方法平均得出,纯化后的FABP的表观分子量为15.0±1.0 kDa。该蛋白的pI值测定为6.8。对来自恶性前列腺组织的纯化FABP与脂肪酸结合的Scatchard分析显示,花生四烯酸的Kd值为0.53±0.02 microM(n = 5)。从良性前列腺组织中纯化的FABP对油酸的Kd值为0.57±0.02 microM,对花生四烯酸的Kd值为0.51±0.04 microM(n = 5)。脂肪酸分析表明,恶性组织来源的FABP中内源性结合的花生四烯酸水平比良性组织来源的高约2.5倍。此外,恶性和良性组织中FABP的浓度相同。恶性和良性组织中FABP的浓度分别为每毫克总胞质蛋白19.2±1.8微克和21.4±2.1微克。(摘要截短为250字)

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