A modified silver staining protocol for visualization of proteins compatible with matrix-assisted laser desorption/ionization and electrospray ionization-mass spectrometry

被引:208
作者
Yan, JX
Wait, R
Berkelman, T
Harry, RA
Westbrook, JA
Wheeler, CH
Dunn, MJ
机构
[1] Harefield Hosp, Heart Sci Ctr, Imperial Coll,Sch Med, Natl Heart & Lung Inst,Dept Cardiothorac Surg, Harefield UB9 6JH, Middx, England
[2] Kennedy Inst Rheumatol, London, England
[3] Amersham Pharmacia Biotech, San Francisco, CA USA
关键词
proteomics; two-dimensional gel electrophoresis; silver stain; mass spectrometry; protein identification; matrix assisted laser desorption/ionization; time of flight; electrospray ionization;
D O I
10.1002/1522-2683(200011)21:17<3666::AID-ELPS3666>3.0.CO;2-6
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The growing availability of genomic sequence information, together with improvements in analytical methodology, have enabled high throughput, high sensitivity protein identification. Silver staining remains the most sensitive method for visualization of proteins separated by two-dimensional gel electrophoresis (2-D PAGE). Several silver staining protocols have been developed which offer improved compatibility with subsequent mass spectrometric analysis. We describe a modified silver staining method that is available as a commercial kit (Silver Stain PlusOne; Amersham Pharmacia Biotech, Amersham, UK). The 2-D patterns obtained with this modified protocol are comparable to those from other silver staining methods. Omitting the sensitizing reagent allows higher loading without saturation, which facilitates protein identification and quantitation. We show that tryptic digests of proteins visualized by the modified stain afford excellent mass spectra by both matrix-assisted laser desorption/ionization and tandem electrospray ionization. We conclude that the modified silver staining protocol is highly compatible with subsequent mass spectrometric analysis.
引用
收藏
页码:3666 / 3672
页数:7
相关论文
共 34 条
[1]
Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]
An integrated approach to proteome analysis: Identification of proteins associated with cardiac hypertrophy [J].
Arnott, D ;
O'Connell, KL ;
King, KL ;
Stults, JT .
ANALYTICAL BIOCHEMISTRY, 1998, 258 (01) :1-18
[3]
Berggren K, 2000, ELECTROPHORESIS, V21, P2509, DOI 10.1002/1522-2683(20000701)21:12<2509::AID-ELPS2509>3.0.CO
[4]
2-9
[5]
Identification of in-gel digested proteins by complementary peptide mass fingerprinting and tandem mass spectrometry data obtained on an electrospray ionization quadrupole time-of-flight mass spectrometer [J].
Borchers, C ;
Peter, JF ;
Hall, MC ;
Kunkel, TA ;
Tomer, KB .
ANALYTICAL CHEMISTRY, 2000, 72 (06) :1163-1168
[6]
Garden RW, 1996, J MASS SPECTROM, V31, P1126, DOI 10.1002/(SICI)1096-9888(199610)31:10<1126::AID-JMS403>3.0.CO
[7]
2-7
[8]
Gharahdaghi F, 1999, ELECTROPHORESIS, V20, P601, DOI 10.1002/(SICI)1522-2683(19990301)20:3<601::AID-ELPS601>3.0.CO
[9]
2-6
[10]
IDENTIFYING PROTEINS FROM 2-DIMENSIONAL GELS BY MOLECULAR MASS SEARCHING OF PEPTIDE-FRAGMENTS IN PROTEIN-SEQUENCE DATABASES [J].
HENZEL, WJ ;
BILLECI, TM ;
STULTS, JT ;
WONG, SC ;
GRIMLEY, C ;
WATANABE, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (11) :5011-5015