Rapid protein identification using N-terminal ''sequence tag'' and amino acid analysis

被引:57
作者
Wilkins, MR
Ou, KL
Appel, RD
Sanchez, JC
Yan, JX
Golaz, O
Farnsworth, V
Cartier, P
Hochstrasser, DF
Williams, KL
Gooley, AA
机构
[1] MACQUARIE UNIV,CTR ANALYT BIOTECHNOL,SYDNEY,NSW 2109,AUSTRALIA
[2] UNIV GENEVA,CENT LAB CLIN CHEM,CH-1211 GENEVA 14,SWITZERLAND
[3] UNIV GENEVA,MED COMP CTR,CH-1211 GENEVA 14,SWITZERLAND
[4] BECKMAN INSTRUMENTS INC,FULLERTON,CA
基金
澳大利亚研究理事会;
关键词
D O I
10.1006/bbrc.1996.0643
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Proteins can be identified by amino acid analysis and database matching, but it is often desirable to increase the confidence in identity through the use of other techniques. Here we describe a rapid protein identification method that uses Edman degradation to create a 3 or 4 amino acid N-terminal ''sequence tag,'' following which proteins are subjected to amino acid analysis protein identification procedures. Edman degradation methods have been modified to take only 23 min per cycle, and rapid amino acid analysis techniques are used. The Edman degradation and amino acid analysis is done on a single PVDF membrane-bound protein sample. A computer database matching program is also presented which uses both amino acid composition and ''sequence tag'' data for protein identification. This method represents the most inexpensive, accurate, and rapid means of protein identification, which is ideal for the screening of proteomes separated by 2-D gel electrophoresis. The creation of N-terminal Edman degradation ''sequence rags'' prior to peptide mass fingerprinting of samples should also be useful. (C) 1996 Academic Press. Inc.
引用
收藏
页码:609 / 613
页数:5
相关论文
共 10 条
[1]  
BAIROCH A, 1994, NUCLEIC ACIDS RES, V22, P3578
[2]   THE FOCUSING POSITIONS OF POLYPEPTIDES IN IMMOBILIZED PH GRADIENTS CAN BE PREDICTED FROM THEIR AMINO-ACID-SEQUENCES [J].
BJELLQVIST, B ;
HUGHES, GJ ;
PASQUALI, C ;
PAQUET, N ;
RAVIER, F ;
SANCHEZ, JC ;
FRUTIGER, S ;
HOCHSTRASSER, D .
ELECTROPHORESIS, 1993, 14 (10) :1023-1031
[3]   CROSS-SPECIES IDENTIFICATION OF PROTEINS SEPARATED BY 2-DIMENSIONAL GEL-ELECTROPHORESIS USING MATRIX-ASSISTED LASER-DESORPTION IONIZATION TIME-OF-FLIGHT MASS-SPECTROMETRY AND AMINO-ACID-COMPOSITION [J].
CORDWELL, SJ ;
WILKINS, MR ;
CERPAPOLJAK, A ;
GOOLEY, AA ;
DUNCAN, M ;
WILLIAMS, KL ;
HUMPHERYSMITH, I .
ELECTROPHORESIS, 1995, 16 (03) :438-443
[4]   PLASMA AND RED-BLOOD-CELL PROTEIN MAPS - UPDATE 1993 [J].
GOLAZ, O ;
HUGHES, GJ ;
FRUTIGER, S ;
PAQUET, N ;
BAIROCH, A ;
PASQUALI, C ;
SANCHEZ, JC ;
TISSOT, JD ;
APPEL, RD ;
WALZER, C ;
BALANT, L ;
HOCHSTRASSER, DF .
ELECTROPHORESIS, 1993, 14 (11) :1223-1231
[5]   AMINO-ACID-ANALYSIS USING DERIVATIZATION WITH 9-FLUORENYLMETHYL CHLOROFORMATE AND REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
HAYNES, PA ;
SHEUMACK, D ;
KIBBY, J ;
REDMOND, JW .
JOURNAL OF CHROMATOGRAPHY, 1991, 540 (1-2) :177-185
[6]   AMINO-ACID-ANALYSIS AND PROTEIN DATABASE COMPOSITIONAL SEARCH AS A RAPID AND INEXPENSIVE METHOD TO IDENTIFY PROTEINS [J].
HOBOHM, U ;
HOUTHAEVE, T ;
SANDER, C .
ANALYTICAL BIOCHEMISTRY, 1994, 222 (01) :202-209
[7]   IDENTIFICATION OF TISSUE PROTEINS BY AMINO-ACID-ANALYSIS AFTER PURIFICATION BY 2-DIMENSIONAL ELECTROPHORESIS [J].
JUNGBLUT, P ;
DZIONARA, M ;
KLOSE, J ;
WITTMANNLEIBOLD, B .
JOURNAL OF PROTEIN CHEMISTRY, 1992, 11 (06) :603-612
[8]   ERROR TOLERANT IDENTIFICATION OF PEPTIDES IN SEQUENCE DATABASES BY PEPTIDE SEQUENCE TAGS [J].
MANN, M ;
WILM, M .
ANALYTICAL CHEMISTRY, 1994, 66 (24) :4390-4399
[9]  
OU K, 1996, IN PRESS J CHROMAT A
[10]   From proteins to proteomes: Large scale protein identification by two-dimensional electrophoresis and amino acid analysis [J].
Wilkins, MR ;
Pasquali, C ;
Appel, RD ;
Ou, K ;
Golaz, O ;
Sanchez, JC ;
Yan, JX ;
Gooley, AA ;
Hughes, G ;
HumpherySmith, I ;
Williams, KL ;
Hochstrasser, DF .
BIO-TECHNOLOGY, 1996, 14 (01) :61-65