Proteomics

被引:23
作者
Arthur, JM
机构
[1] Med Univ S Carolina, Div Nephrol, Dept Med, Charleston, SC 29425 USA
[2] Ralph H Johnson Med Ctr, Charleston, SC USA
关键词
proteomics; protein expression; protein function;
D O I
10.1097/00041552-200307000-00011
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review Proteomics encompasses a group of technologies that attempt to separate, identify and characterize a global set of proteins. This review will highlight the technologies available, outline the capabilities, advantages and disadvantages of each and briefly describe applications in nephrology. Recent findings Proteomics provides information about abundance, location, chemical modification and protein-protein interactions that is not available from genomic technologies. Several proteomic approaches are now widely available. Liquid chromatography/mass spectrometry, two-dimensional gel electrophoresis, antibody arrays and protein chips (surface enhanced laser desorption ionization) provide opportunities to identify and compare an abundance of proteins as well as to determine posttranslational modifications, subcellular location and molecular interactions. Recent advances such as multidimensional chromatographic analysis and isotope coded affinity tags have expanded the usefulness of these approaches. Summary Proteomic technologies are improving and developing rapidly. These techniques will be valuable tools to develop markers for disease, identify and evaluate proteins as drug targets and understand renal physiology at the protein level.
引用
收藏
页码:423 / 430
页数:8
相关论文
共 45 条
[1]   New insights into cyclosporine A nephrotoxicity by proteome analysis [J].
Aicher, L ;
Wahl, D ;
Arce, A ;
Grenet, O ;
Steiner, S .
ELECTROPHORESIS, 1998, 19 (11) :1998-2003
[2]   A comparison of selected mRNA and protein abundances in human liver [J].
Anderson, L ;
Seilhamer, J .
ELECTROPHORESIS, 1997, 18 (3-4) :533-537
[3]  
ANDERSON NG, 1979, CLIN CHEM, V25, P1199
[4]   Differential expression of proteins in renal cortex and medulla: A proteomic approach [J].
Arthur, JM ;
Thongboonkerd, V ;
Scherzer, JA ;
Cai, J ;
Pierce, WM ;
Klein, JB .
KIDNEY INTERNATIONAL, 2002, 62 (04) :1314-1321
[5]  
Berggren K, 2000, ELECTROPHORESIS, V21, P2509, DOI 10.1002/1522-2683(20000701)21:12<2509::AID-ELPS2509>3.0.CO
[6]  
2-9
[7]  
Cho A, 2002, SCIENCE, V298, P527
[8]  
Cutler P, 1999, ELECTROPHORESIS, V20, P3647, DOI 10.1002/(SICI)1522-2683(19991201)20:18<3647::AID-ELPS3647>3.0.CO
[9]  
2-#
[10]   Quantitative proteomic analysis using a MALDI quadrupole time-of-flight mass spectrometer [J].
Griffin, TJ ;
Gygi, SP ;
Rist, B ;
Aebersold, R ;
Loboda, A ;
Jilkine, A ;
Ens, W ;
Standing, KG .
ANALYTICAL CHEMISTRY, 2001, 73 (05) :978-986