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通过改良的二维电泳技术对肝窦内皮细胞膜进行蛋白质组学分析。

Proteomics analysis of plasma membrane from liver sinusoidal endothelial cells after partial hepatectomy by an improved two-dimensional electrophoresis.

机构信息

Key Laboratory of Protein Chemistry and Developmental Biology of Ministry of Education, College of Life Sciences, Hunan Normal University, Changsha, People's Republic of China.

出版信息

Mol Cell Biochem. 2010 Nov;344(1-2):137-50. doi: 10.1007/s11010-010-0537-z. Epub 2010 Jul 6.

Abstract

Liver regeneration is an angiogenesis-associated phenomenon. To identify key plasma membrane (PM) proteins of endothelial cells involved in the initiation of angiogenesis during liver regeneration, the PM of liver sinusoidal endothelial cells (LSEC) at 72 h after partial hepatectomy was enriched by an established in vivo membrane density perturbation method. The differentially expressed membrane proteins compared to those from sham operation were quantified using an improved two-dimensional 16-BAC/SDS-PAGE and identified by LC-MS/MS. Several proteins were further confirmed by cICAT labeling quantitative strategy. A total of 47 proteins were identified including known and novel proteins involved in angiogenesis or liver regeneration, such as inducible nitric oxide synthase, type IV collagen, and integrin beta3. Our results indicated that the combination of the membrane density perturbation strategy and the improved two-dimensional electrophoresis (2-DE) method are useful for investigating the endothelial dysfunctions in vivo.

摘要

肝脏再生是一种血管生成相关的现象。为了鉴定在肝再生过程中血管生成起始阶段涉及的内皮细胞关键质膜(PM)蛋白,通过已建立的体内膜密度扰动方法富集了部分肝切除后 72 小时的肝窦内皮细胞(LSEC)的 PM。使用改良的二维 16-BAC/SDS-PAGE 并通过 LC-MS/MS 对与 sham 手术相比差异表达的膜蛋白进行定量。通过 cICAT 标记定量策略进一步验证了几种蛋白质。总共鉴定出 47 种蛋白质,包括已知和新的参与血管生成或肝再生的蛋白质,如诱导型一氧化氮合酶、IV 型胶原和整合素β3。我们的结果表明,膜密度扰动策略和改良的二维电泳(2-DE)方法的结合可用于研究体内内皮功能障碍。

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