首页> 外文期刊>Analytical and bioanalytical chemistry >Precipitation and selective extraction of human serum endogenous peptides with analysis by quadrupole time-of-flight mass spectrometry reveals posttranslational modifications and low-abundance peptides
【24h】

Precipitation and selective extraction of human serum endogenous peptides with analysis by quadrupole time-of-flight mass spectrometry reveals posttranslational modifications and low-abundance peptides

机译:通过四极杆飞行时间质谱分析对人血清内源肽进行沉淀和选择性提取,揭示了翻译后修饰和低丰度肽

获取原文
获取原文并翻译 | 示例
       

摘要

The endogenous peptides of human serum may have regulatory functions, have been associated with physiological states, and their modifications may reveal some mechanisms of disease. In order to correlate levels of specific peptides with disease alongside internal standards, the polypeptides must first be reliably extracted and identified. Endogenous blood peptides can be effectively enriched by precipitation of the serum with organic solvents followed by selective extraction of peptides using aqueous solutions modified with organic solvents. Polypeptides on filter paper were assayed with Coomasie brilliant blue binding. The polypeptides were resolved by detergent tricine polyacrylamide electrophoresis and visualized by diamine silver staining. Peptides in the extracts were collected by C18 and analyzed by matrix-assisted laser desorption/ionization and liquid chromatography-electrospray ionization-tandem mass spectrometry (MS/MS) quadrupole time-of-flight MS/MS. Peptides were resolved as multiple isotopic peaks in MS mode with mass deviation of 0.1 Da or less and similar accuracy for fragments. The sensitivity of MS and MS/MS analysis was estimated to be in the picomolar range or less. The peptide composition of the extracts was dependent on solvent formulation. Multiple peptides from apolipoproteins, complement proteins, coagulation factors, and many others were identified by X!Tandem with high mass accuracy of peptide ions and fragments from collision-induced dissociation. Many previously unreported posttranslational modifications of peptides including phosphorylations, oxidations, glycosylations, and others were detected with high mass accuracy and may be of clinical importance. About 4,630 redundant peptides were identified with 99% confidence separately, and together some 1,251 distinct proteins were identified with 99% confidence or greater using the Paragon algorithm.
机译:人血清中的内源肽可能具有调节功能,并与生理状态有关,它们的修饰可能揭示某些疾病机理。为了使特定肽的水平与疾病以及内标相关联,必须首先可靠地提取和鉴定多肽。通过用有机溶剂沉淀血清,然后使用经有机溶剂修饰的水溶液选择性提取肽,可以有效地富集内源性血肽。用考马斯亮蓝结合法测定滤纸上的多肽。通过去污剂三胺聚丙烯酰胺电泳分离多肽,并通过二胺银染色可视化。提取物中的肽通过C18收集,并通过基质辅助激光解吸/电离和液相色谱-电喷雾电离-串联质谱(MS / MS)四极杆飞行时间MS / MS进行分析。肽在MS模式下解析为多个同位素峰,质量偏差为0.1 Da或更小,且片段的准确度相似。 MS和MS / MS分析的灵敏度估计在皮摩尔范围或更小。提取物的肽组成取决于溶剂配方。 X!Tandem鉴定了载脂蛋白,补体蛋白,凝血因子和许多其他多肽中的多种肽,这些肽具有高质量的肽离子和碰撞诱导的解离片段。已检测出许多以前未报道的肽的翻译后修饰,包括磷酸化,氧化,糖基化等,这些修饰的质量准确度很高,可能具有临床重要性。分别以99%的置信度鉴定出约4,630个冗余肽,并使用Paragon算法以99%的置信度或更高鉴定了约1,251个不同的蛋白质。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号