Targeted Quantitation of HMGB1 Protein by label-free Mass Spectrometry Technique

被引:0
作者
Manfredi, Marcello [1 ,2 ]
Martinotti, Simona [1 ]
Patrone, Mauro [1 ]
Sassi, Maria Paola [3 ]
Ranzato, Elia [1 ]
Marengo, Emilio [1 ]
机构
[1] Univ Piemonte Orientale, Dept Sci & Technol Innovat, Alessandria, Italy
[2] Univ Piemonte Orientale, ISALIT Srl, Alessandria, Italy
[3] Ist Nazl Ric Metrol, Turin, Italy
来源
2015 IEEE INTERNATIONAL SYMPOSIUM ON MEDICAL MEASUREMENTS AND APPLICATIONS (MEMEA) PROCEEDINGS | 2015年
关键词
Targeted proteomics; shotgun analysis; HMGB1; quantification; PROTEOMICS; QUANTIFICATION; IDENTIFICATION;
D O I
暂无
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Mass spectrometry (MS)-based methods have become popular in recent years for the quantitation of biomolecules, especially peptides and proteins. High Mobility Group Box-1 protein (HMGB1) is a nuclear DNA-binding protein that resides inside the nucleus and can be released to the extracellular space under specific conditions. HMGB1 has been reported as circulating mechanistic indicators of cell death mode in animal models and in clinical studies. There is accumulating evidence that HMGB1 contributes to the pathogenesis of inflammatory and autoimmune diseases. Moreover, HMGB1 has been found to play an important role in tumor development, growth, and spread. Circulating HMGB1 level could be a useful and specific marker for evaluating different disease status and predicting prognosis in patients. The label-free quantitative comparison without any standard reference or normalization of the target peptide signal is the simplest Liquid Chromatographic-MS (LC-MS) method for the quantitation of a protein. The aim of the research was the development of an analytical method for the quantitation of HMGB1 by a label-free Mass Spectrometry technique. In this paper are presented the preliminary results: the quantitation of HMGB1 was assessed in a cell lysate sample through the use of the standard concentration curve of purified HMGB1 protein.
引用
收藏
页码:526 / 530
页数:5
相关论文
共 14 条
[1]  
Brewis IA, 2010, ADV PROTEIN CHEM STR, V80, P1, DOI [10.1016/B978-0-12-381264-3.00001-1, 10.1016/S1876-1623(10)80001-X]
[2]   Review of software tools for design and analysis of large scale MRM proteomic datasets [J].
Colangelo, Christopher M. ;
Chung, Lisa ;
Bruce, Can ;
Cheung, Kei-Hoi .
METHODS, 2013, 61 (03) :287-298
[3]   IDENTIFICATION AND QUANTIFICATION OF PROTEIN POSTTRANSLATIONAL MODIFICATIONS [J].
Farley, Adam R. ;
Link, Andrew J. .
GUIDE TO PROTEIN PURIFICATION, SECOND EDITION, 2009, 463 :725-763
[4]   Selected reaction monitoring for quantitative proteomics: a tutorial [J].
Lange, Vinzenz ;
Picotti, Paola ;
Domon, Bruno ;
Aebersold, Ruedi .
MOLECULAR SYSTEMS BIOLOGY, 2008, 4 (1)
[5]   Targeted Quantitation of Proteins by Mass Spectrometry [J].
Liebler, Daniel C. ;
Zimmerman, Lisa J. .
BIOCHEMISTRY, 2013, 52 (22) :3797-3806
[6]  
Miller JN., 2000, STAT CHEMOMETRICS AN, V4th
[7]   Parallel Reaction Monitoring for High Resolution and High Mass Accuracy Quantitative, Targeted Proteomics [J].
Peterson, Amelia C. ;
Russell, Jason D. ;
Bailey, Derek J. ;
Westphall, Michael S. ;
Coon, Joshua J. .
MOLECULAR & CELLULAR PROTEOMICS, 2012, 11 (11) :1475-1488
[8]  
Picotti P, 2012, NAT METHODS, V9, P555, DOI [10.1038/NMETH.2015, 10.1038/nmeth.2015]
[9]  
Ranzato Elia, 2012, Cells, V1, P699, DOI 10.3390/cells1040699
[10]   Spreading of Mesothelioma Cells Is Rapamycin-Sensitive and Requires Continuing Translation [J].
Ranzato, Elia ;
Grosso, Stefano ;
Patrone, Mauro ;
Betta, Pier Giacomo ;
Viarengo, Aldo ;
Biffo, Stefano .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2009, 108 (04) :867-876