SEQUENCE-ANALYSIS OF PROTEINS SEPARATED BY POLYACRYLAMIDE-GEL ELECTROPHORESIS - TOWARDS AN INTEGRATED PROTEIN DATABASE

被引:55
作者
AEBERSOLD, R [1 ]
LEAVITT, J [1 ]
机构
[1] INST MED RES,SAN JOSE,CA 95128
关键词
D O I
10.1002/elps.1150110702
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Improved technologies or the synergistic use of complementary methods enhance the efficiency of research and permit the exploration of new approaches for the investigation of complex problems. High sensitivity protein sequence analysis and polyacrylamide gel electrophoresis are such complementary methods. Here we summarize the current status of high sensitivity sequence analysis of proteins separated in polyacrylamide gels and discuss strategies by which this technology can cnhance biological research by generating new approaches for the solution of complex, multifacetted problems. Finally, we outline lmminent technological advances in the area of high sensitivity protein sequence analysis and argue that further technological developments will ultimately lead to the generation of an integrated protein database (containing structural and functional as well as physiological information in an easily accessible form) of all the proteins separated by high resolution two‐dimensional gel electrophoresis. Copyright © 1990 VCH Verlagsgesellschaft mbH
引用
收藏
页码:517 / 527
页数:11
相关论文
共 89 条
[11]   ANALYTICAL TECHNIQUES FOR CELL FRACTIONS .21. 2-DIMENSIONAL ANALYSIS OF SERUM AND TISSUE PROTEINS - MULTIPLE ISOELECTRIC-FOCUSING [J].
ANDERSON, NG ;
ANDERSON, NL .
ANALYTICAL BIOCHEMISTRY, 1978, 85 (02) :331-340
[12]  
ANDERSON NL, 1985, ELECTROPHORESIS, V6, P592
[13]  
BARAN MD, 1987, J BIOL CHEM, V262, P17623
[14]  
BATAILLE N, 1987, YEAST, V2, P1
[15]   PROTEIN-ELECTROBLOTTING AND PROTEIN-MICROSEQUENCING STRATEGIES IN GENERATING PROTEIN DATA-BASES FROM TWO-DIMENSIONAL GELS - (COMPUTERIZED PROTEIN DATA-BASES HUMAN GENOME SEQUENCING) [J].
BAUW, G ;
VANDAMME, J ;
PUYPE, M ;
VANDEKERCKHOVE, J ;
GESSER, B ;
RATZ, GP ;
LAURIDSEN, JB ;
CELIS, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (20) :7701-7705
[16]   HIGH-SENSITIVITY SEQUENCE DETERMINATION OF PROTEINS QUANTITATIVELY RECOVERED FROM SODIUM DODECYL-SULFATE GELS USING AN IMPROVED ELECTRODIALYSIS PROCEDURE [J].
BHOWN, AS ;
MOLE, JE ;
HUNTER, F ;
BENNETT, JC .
ANALYTICAL BIOCHEMISTRY, 1980, 103 (01) :184-190
[17]   ISOELECTRIC-FOCUSING IN IMMOBILIZED PH GRADIENTS - PRINCIPLE, METHODOLOGY AND SOME APPLICATIONS [J].
BJELLQVIST, B ;
EK, K ;
RIGHETTI, PG ;
GIANAZZA, E ;
GORG, A ;
WESTERMEIER, R ;
POSTEL, W .
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 1982, 6 (04) :317-339
[18]   CYCLIN PCNA IS THE AUXILIARY PROTEIN OF DNA POLYMERASE-DELTA [J].
BRAVO, R ;
FRANK, R ;
BLUNDELL, PA ;
MACDONALDBRAVO, H .
NATURE, 1987, 326 (6112) :515-517
[19]   IDENTIFICATION OF A NUCLEAR AND OF A CYTOPLASMIC POLYPEPTIDE WHOSE RELATIVE PROPORTIONS ARE SENSITIVE TO CHANGES IN THE RATE OF CELL-PROLIFERATION [J].
BRAVO, R ;
FEY, SJ ;
BELLATIN, J ;
LARSEN, PM ;
AREVALO, J ;
CELIS, JE .
EXPERIMENTAL CELL RESEARCH, 1981, 136 (02) :311-319
[20]  
BRAVO R, 1982, CLIN CHEM, V28, P766