Literature DB >> 2010434

Activation and regulation of protein kinase C enzymes.

G L Nelsestuen1, M D Bazzi.   

Abstract

Protein Kinase C (PKC) has been a principal regulatory enzyme whose function has been intensely investigated in the past decade. The primary features of this family of enzymes includes phosphorylation of serine and threonine residues located on basic proteins and peptide in a manner that is stimulated by calcium, phospholipid, and either diacylglycerol or phorbol esters. An additional intriguing feature of the enzymes is its ability to form two membrane-associated states, one of which is calcium dependent and reversible and the second is an irreversible complex which has the characteristics of an intrinsic membrane protein. Formation of the irreversible membrane-bound form is greatly facilitated by calcium and the tumor-promoting phorbol esters but does not appear to include covalent changes in the PKC structure. The intrinsic membrane-bound form is a very different enzyme in that its activity is no longer dependent on the other cofactors. It is proposed that formation of the irreversible membrane-bound form may be a mechanism for generating long-term cell regulation events where transient cell signals and second messengers induce long-term changes in the distribution of an enzyme in the cell. This property may be common to a number of regulatory proteins that are known to be distributed between the cytosol and membrane-fractions in the cell. Unfortunately, many problems have confronted study of PKC mechanism using the in vitro assay. This assay involves aggregation of the substrate, phospholipid, and enzyme to form a discontinuous mixture. Such a complex system prevents straightforward interpretation of enzyme kinetic data. Although many compounds affect the in vitro activity of PKC, most appear to accomplish this by relatively uninteresting mechanisms such as interference with the aggregation process. While some highly potent inhibitors undoubtedly interact directly with PKC, they also inhibit other enzymes and there are no entirely specific inhibitors of PKC known. Speculation on the possible roles of PKC in cell regulation are abundant and exciting. However, delineation of the regulatory roles of PKC may require another decade of intense effort.

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Year:  1991        PMID: 2010434     DOI: 10.1007/bf00768838

Source DB:  PubMed          Journal:  J Bioenerg Biomembr        ISSN: 0145-479X            Impact factor:   2.945


  111 in total

1.  Structure of Ca2+ prothrombin fragment 1 including the conformation of the Gla domain.

Authors:  M Soriano-Garcia; C H Park; A Tulinsky; K G Ravichandran; E Skrzypczak-Jankun
Journal:  Biochemistry       Date:  1989-08-22       Impact factor: 3.162

Review 2.  Staurosporine, K-252 and UCN-01: potent but nonspecific inhibitors of protein kinases.

Authors:  U T Rüegg; G M Burgess
Journal:  Trends Pharmacol Sci       Date:  1989-06       Impact factor: 14.819

3.  The complete primary structure of protein kinase C--the major phorbol ester receptor.

Authors:  P J Parker; L Coussens; N Totty; L Rhee; S Young; E Chen; S Stabel; M D Waterfield; A Ullrich
Journal:  Science       Date:  1986-08-22       Impact factor: 47.728

4.  Ca2+-independent activation of protease-activated kinase II by phospholipids/diolein and comparison with the Ca2+/phospholipid-dependent protein kinase.

Authors:  M I Gonzatti-Haces; J A Traugh
Journal:  J Biol Chem       Date:  1986-11-15       Impact factor: 5.157

5.  Purification of the major protein-tyrosine-phosphatases of human placenta.

Authors:  N K Tonks; C D Diltz; E H Fischer
Journal:  J Biol Chem       Date:  1988-05-15       Impact factor: 5.157

6.  Substrate specificity of protein kinase C. Use of synthetic peptides corresponding to physiological sites as probes for substrate recognition requirements.

Authors:  J R Woodgett; K L Gould; T Hunter
Journal:  Eur J Biochem       Date:  1986-11-17

7.  Polyamines inhibit phospholipid-sensitive and calmodulin-sensitive Ca2+-dependent protein kinases.

Authors:  D F Qi; R C Schatzman; G J Mazzei; R S Turner; R L Raynor; S Liao; J F Kuo
Journal:  Biochem J       Date:  1983-08-01       Impact factor: 3.857

8.  Tissue-specific expression of three distinct types of rabbit protein kinase C.

Authors:  S Ohno; H Kawasaki; S Imajoh; K Suzuki; M Inagaki; H Yokokura; T Sakoh; H Hidaka
Journal:  Nature       Date:  1987 Jan 8-14       Impact factor: 49.962

9.  Activation of calcium and phospholipid-dependent protein kinase by diacylglycerol, its possible relation to phosphatidylinositol turnover.

Authors:  A Kishimoto; Y Takai; T Mori; U Kikkawa; Y Nishizuka
Journal:  J Biol Chem       Date:  1980-03-25       Impact factor: 5.157

10.  Weak inhibition of protein kinase C coupled with various non-specific effects make sphingosine an unsuitable tool in platelet signal transduction studies.

Authors:  S Krishnamurthi; Y Patel; V V Kakkar
Journal:  Biochim Biophys Acta       Date:  1989-02-09
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  12 in total

Review 1.  Mechanism of action of volatile anesthetics: role of protein kinase C.

Authors:  Renato Santiago Gomez; Cristina Guatimosim; Marcus Vinicius Gomez
Journal:  Cell Mol Neurobiol       Date:  2003-12       Impact factor: 5.046

Review 2.  The role of protein kinase C and its neuronal substrates dephosphin, B-50, and MARCKS in neurotransmitter release.

Authors:  P J Robinson
Journal:  Mol Neurobiol       Date:  1991       Impact factor: 5.590

3.  Nociceptor beta II, delta, and epsilon isoforms of PKC differentially mediate paclitaxel-induced spontaneous and evoked pain.

Authors:  Ying He; Zaijie Jim Wang
Journal:  J Neurosci       Date:  2015-03-18       Impact factor: 6.167

4.  Characterization of sgk, a novel member of the serine/threonine protein kinase gene family which is transcriptionally induced by glucocorticoids and serum.

Authors:  M K Webster; L Goya; Y Ge; A C Maiyar; G L Firestone
Journal:  Mol Cell Biol       Date:  1993-04       Impact factor: 4.272

Review 5.  Spinal and afferent PKC signaling mechanisms that mediate chronic pain in sickle cell disease.

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Journal:  Neurosci Lett       Date:  2019-04-30       Impact factor: 3.046

6.  Effects of diacylglycerols and Ca2+ on structure of phosphatidylcholine/phosphatidylserine bilayers.

Authors:  E M Goldberg; D S Lester; D B Borchardt; R Zidovetzki
Journal:  Biophys J       Date:  1994-02       Impact factor: 4.033

7.  Phorbol 12-myristate 13-acetate-stimulated phosphorylation of erythrocyte membrane skeletal proteins is blocked by calpain inhibitors: possible role of protein kinase M.

Authors:  Z Al; C M Cohen
Journal:  Biochem J       Date:  1993-12-15       Impact factor: 3.857

8.  Inactive membrane protein kinase Cs: a possible target for receptor signalling.

Authors:  B R Chakravarthy; J F Whitfield; J P Durkin
Journal:  Biochem J       Date:  1994-12-15       Impact factor: 3.857

Review 9.  Membranes: a meeting point for lipids, proteins and therapies.

Authors:  Pablo V Escribá; José M González-Ros; Félix M Goñi; Paavo K J Kinnunen; Lászlo Vigh; Lissete Sánchez-Magraner; Asia M Fernández; Xavier Busquets; Ibolya Horváth; Gwendolyn Barceló-Coblijn
Journal:  J Cell Mol Med       Date:  2008-02-08       Impact factor: 5.310

10.  Effects of diacylglycerols on conformation of phosphatidylcholine headgroups in phosphatidylcholine/phosphatidylserine bilayers.

Authors:  E M Goldberg; D S Lester; D B Borchardt; R Zidovetzki
Journal:  Biophys J       Date:  1995-09       Impact factor: 4.033

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