Physiological inhibitors or protein kinase C

被引:6
作者
Melner, MH [1 ]
机构
[1] VANDERBILT UNIV,SCH MED,DEPT CELL BIOL,NASHVILLE,TN 37232
关键词
protein kinase C; inhibitor; signal transduction;
D O I
10.1016/0006-2952(95)02196-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Increasing numbers of proteins that have the capacity of interacting with protein kinase C isozymes in vitro and inhibiting their enzymatic activity in a noncompetitive manner have been purified. While these proteins can be hypothesized to be part of a tight regulatory system for protein kinase C enzymatic activity, critical examinations of the roles of these proteins in the context of whole cells have not yet been performed. Interesting new data suggest that some of the classes of protein kinase C inhibitors may have a much broader role of interacting with multiple types of kinases and proto-oncogene products. cDNAs encoding a number of these inhibitor proteins have been isolated, which will allow the design and implementation of experiments on their cell biology and help address their function outside of the context of their operational definitions.
引用
收藏
页码:869 / 877
页数:9
相关论文
共 79 条
[1]  
AITKEN A, 1990, NATURE, V344, P594
[2]   THE ROLE OF SPECIFIC ISOFORMS OF 14-3-3 PROTEIN IN REGULATING PROTEIN-KINASE ACTIVITY IN THE BRAIN [J].
AITKEN, A ;
AMESS, B ;
HOWELL, S ;
JONES, D ;
MARTIN, H ;
PATEL, Y ;
ROBINSON, K ;
TOKER, A .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1992, 20 (03) :607-611
[3]   14-3-3 PROTEINS - A HIGHLY CONSERVED, WIDESPREAD FAMILY OF EUKARYOTIC PROTEINS [J].
AITKEN, A ;
COLLINGE, DB ;
VANHEUSDEN, BPH ;
ISOBE, T ;
ROSEBOOM, PH ;
ROSENFELD, G ;
SOLL, J .
TRENDS IN BIOCHEMICAL SCIENCES, 1992, 17 (12) :498-501
[4]   CDNA CLONING AND CHARACTERIZATION OF MITOCHONDRIAL IMPORT STIMULATION FACTOR (MSF) PURIFIED FROM RAT-LIVER CYTOSOL [J].
ALAM, R ;
HACHIYA, N ;
SAKAGUCHI, M ;
KAWABATA, S ;
IWANAGA, S ;
KITAJIMA, M ;
MIHARA, K ;
OMURA, T .
JOURNAL OF BIOCHEMISTRY, 1994, 116 (02) :416-425
[5]  
BALAZOVICH KJ, 1986, J IMMUNOL, V137, P1665
[6]   PURIFICATION OF PKC-I, AN ENDOGENOUS PROTEIN-KINASE-C INHIBITOR, AND TYPE-II AND TYPE-III PROTEIN-KINASE-C ISOENZYMES FROM HUMAN NEUTROPHILS [J].
BALAZOVICH, KJ ;
MCEWEN, EL ;
LUTZKE, ML ;
BOXER, LA ;
WHITE, T .
BIOCHEMICAL JOURNAL, 1992, 284 :399-405
[7]   PROTEIN-KINASE-C AND ANNEXINS - UNUSUAL CALCIUM RESPONSE ELEMENTS IN THE CELL [J].
BAZZI, MD ;
NELSESTUEN, GL .
CELLULAR SIGNALLING, 1993, 5 (04) :357-365
[8]   THERAPEUTIC POTENTIAL OF PROTEIN-KINASE-C INHIBITORS [J].
BRADSHAW, D ;
HILL, CH ;
NIXON, JS ;
WILKINSON, SE .
AGENTS AND ACTIONS, 1993, 38 (1-2) :135-147
[9]   DIFFERENT AND RAPID RESPONSES OF 4 CYANOBACTERIAL PSBA TRANSCRIPTS TO CHANGES IN LIGHT-INTENSITY [J].
BUSTOS, SA ;
SCHAEFER, MR ;
GOLDEN, SS .
JOURNAL OF BACTERIOLOGY, 1990, 172 (04) :1998-2004
[10]   INHIBITION OF PROTEIN KINASE-C BY DEFENSINS, ANTIBIOTIC PEPTIDES FROM HUMAN-NEUTROPHILS [J].
CHARP, PA ;
RICE, WG ;
RAYNOR, RL ;
REIMUND, E ;
KINKADE, JM ;
GANZ, T ;
SELSTED, ME ;
LEHRER, RI ;
KUO, JF .
BIOCHEMICAL PHARMACOLOGY, 1988, 37 (05) :951-956