MRMaid-DB: A Repository of Published SRM Transitions

被引:16
作者
Cham , Jennifer A. [1 ]
Bianco, Luca [1 ]
Barton, Chris [2 ]
Bessant, Conrad [1 ]
机构
[1] Cranfield Univ, Bioinformat Grp, Cranfield MK43 0AL, Beds, England
[2] Quotient Biores Ltd, Fordham CB7 5WW, Cambs, England
基金
英国生物技术与生命科学研究理事会; 英国工程与自然科学研究理事会;
关键词
Biomart; database; multiple reaction monitoring (MRM); selected reaction monitoring (SRM); Web-based; CHROMATOGRAPHY/TANDEM MASS-SPECTROMETRY; REACTION MONITORING ASSAYS; PLASMA-PROTEINS; QUANTIFICATION; QUANTITATION; DATABASES; SERUM;
D O I
10.1021/pr900713u
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Selected reaction monitoring (SRM) is a technique that applies tandem mass spectrometry to quantify specific proteins of biological interest. The key to SRM is finding the best peptide-to-product ion transitions to monitor. The MRMaid database (MRMaid-DB) is a new online database for capturing SRM transitions from published research papers to save practitioners time when searching for transitions that have been previously validated. It contains all the information needed to reproduce the transitions, such as information on the sample matrix HPLC, and MS instrumentation used, and also includes details of the manuscript of origin. Transitions are submitted using simple Web-based data entry forms, meaning researchers have a simple way to increase access to their transitions, and in turn, may increase the citations for their research papers. MRMaid-DB is free to use, via the Web at www.mrmaid-db.info.
引用
收藏
页码:620 / 625
页数:6
相关论文
共 21 条
[1]   Quantitative mass spectrometric multiple reaction monitoring assays for major plasma proteins [J].
Anderson, L ;
Hunter, CL .
MOLECULAR & CELLULAR PROTEOMICS, 2006, 5 (04) :573-588
[2]   Multiplexed LC-MS/MS analysis of horse plasma proteins to study doping in sport [J].
Barton, Chris ;
Beck, Paul ;
Kay, Richard ;
Teale, Phil ;
Roberts, Jane .
PROTEOMICS, 2009, 9 (11) :3058-3065
[3]   The Protein Identifier Cross-Referencing (PICR) service:: reconciling protein identifiers across multiple source databases [J].
Cote, Richard G. ;
Jones, Philip ;
Martens, Lennart ;
Kerrien, Samuel ;
Reisinger, Florian ;
Lin, Quan ;
Leinonen, Rasko ;
Apweiler, Rolf ;
Hermjakob, Henning .
BMC BIOINFORMATICS, 2007, 8 (1) :401
[4]  
Cox David M, 2005, J Biomol Tech, V16, P83
[5]  
DEUTSCH EW, 2009, TRAML TRANSITIONS MA
[6]   BioMart and Bioconductor: a powerful link between biological databases and microarray data analysis [J].
Durinck, S ;
Moreau, Y ;
Kasprzyk, A ;
Davis, S ;
De Moor, B ;
Brazma, A ;
Huber, W .
BIOINFORMATICS, 2005, 21 (16) :3439-3440
[7]   Absolute quantification of proteins and phosphoproteins from cell lysates by tandem MS [J].
Gerber, SA ;
Rush, J ;
Stemman, O ;
Kirschner, MW ;
Gygi, SP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (12) :6940-6945
[8]   The application of ultra-performance liquid chromatography/tandem mass spectrometry to the detection and quantitation of apolipoproteins in human serum [J].
Kay, Richard G. ;
Gregory, Barbara ;
Grace, Philip B. ;
Pleasance, Steve .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2007, 21 (16) :2585-2593
[9]   Quantitative, multiplexed assays for low abundance proteins in plasma by targeted mass spectrometry and stable isotope dilution [J].
Keshishian, Hasmik ;
Addona, Terri ;
Burgess, Michael ;
Kuhn, Eric ;
Carr, Steven A. .
MOLECULAR & CELLULAR PROTEOMICS, 2007, 6 (12) :2212-2229
[10]   Quantification of C-reactive protein in the serum of patients with rheumatoid arthritis using multiple reaction monitoring mass spectrometry and 13C-labeled peptide standards [J].
Kuhn, E ;
Wu, J ;
Karl, J ;
Liao, H ;
Zolg, W ;
Guild, B .
PROTEOMICS, 2004, 4 (04) :1175-1186