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使用液相色谱/质谱法进行蛋白水解肽靶向的诊断性蛋白质发现。

Diagnostic protein discovery using liquid chromatography/mass spectrometry for proteolytic peptide targeting.

作者信息

Koomen John M, Zhao Haitao, Li Donghui, Nasser Waleed, Hawke David H, Abbruzzese James L, Baggerly Keith A, Kobayashi Ryuji

机构信息

Molecular Pathology, University of Texas M.D. Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX 77030, USA.

出版信息

Rapid Commun Mass Spectrom. 2005;19(12):1624-36. doi: 10.1002/rcm.1963.

Abstract

A peptide targeting method has been developed for diagnostic protein discovery, which combines proteolytic digestion of fractionated plasma proteins and liquid chromatography coupled to electrospray time-of-flight mass spectrometry (LC/ESI-TOFMS) profiling. Proteolysis prior to profiling overcomes molecular weight limitations and compensates for the poor sensitivity of matrix-assisted laser desorption/ionization (MALDI) protein profiling. LC/MS increases the peak capacity compared to crude fractionation techniques or single sample MALDI analysis. Differentially expressed peptides are targeted in the mass chromatograms using bioinformatic techniques and subsequently sequenced with MALDI tandem MS. In a model study comparing pancreatic cancer patients to controls, 74% of the peptide targets were successfully sequenced. This profiling method was superior to previous experiments using single sample MALDI analysis for protein profiling or proteolytic peptide profiling, because more potential protein markers were identified.

摘要

一种用于诊断性蛋白质发现的肽靶向方法已经被开发出来,该方法结合了分级血浆蛋白的蛋白酶解和液相色谱与电喷雾飞行时间质谱(LC/ESI-TOFMS)分析。在分析之前进行蛋白酶解克服了分子量限制,并弥补了基质辅助激光解吸/电离(MALDI)蛋白质分析灵敏度低的问题。与粗分级技术或单一样品MALDI分析相比,LC/MS增加了峰容量。使用生物信息学技术在质量色谱图中靶向差异表达的肽,随后用MALDI串联质谱进行测序。在一项将胰腺癌患者与对照进行比较的模型研究中,74%的肽靶点被成功测序。这种分析方法优于先前使用单一样品MALDI分析进行蛋白质分析或蛋白水解肽分析的实验,因为鉴定出了更多潜在的蛋白质标志物。

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