Mechanism of inhibition of protein kinase C by 14-3-3 isoforms. 14-3-3 isoforms do not have phospholipase A2 activity

Biochem J. 1994 May 1;299 ( Pt 3)(Pt 3):853-61. doi: 10.1042/bj2990853.

Abstract

The ability of individual members of the 14-3-3 protein family to inhibit protein kinase C (PKC) has been studied by using a synthetic peptide based on the specific 80 kDa substrate for PKC (MARCKS protein) in two different assay systems. Recombinant 14-3-3 and isoforms renatured by a novel method after separation by reverse-phase h.p.l.c. were studied. The detailed effects of diacylglycerol and the phorbol ester phorbol 12-myristate 13-acetate on the inhibition were also investigated. This suggests that one of the sites of interaction of 14-3-3 may be the cysteine-rich (C1) domain in PKC. Since a region in secreted phospholipase A2 (PLA2) shares similarity with this domain, the ability of 14-3-3 to interact with mammalian PLA2 was studied. Cytosolic PLA2 has some similarity to the C2 region of PKC, and the effect of 14-3-3 on this class of PLA2 was also analysed. In contrast with a previous report, no PLA2 activity was found in brain 14-3-3, nor in any of the recombinant proteins tested. These include zeta 14-3-3 isoform, on which the original observation was made.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 14-3-3 Proteins
  • Amino Acid Sequence
  • Animals
  • Calcium / metabolism
  • Chromatography, High Pressure Liquid
  • Circular Dichroism
  • Electrophoresis, Gel, Two-Dimensional
  • Humans
  • Mass Spectrometry
  • Molecular Sequence Data
  • Nerve Tissue Proteins / metabolism
  • Nerve Tissue Proteins / pharmacology*
  • Phospholipases A / metabolism*
  • Phospholipases A2
  • Phospholipids / metabolism
  • Protein Kinase C / antagonists & inhibitors*
  • Sequence Homology, Amino Acid
  • Sheep
  • Substrate Specificity
  • Tyrosine 3-Monooxygenase*

Substances

  • 14-3-3 Proteins
  • Nerve Tissue Proteins
  • Phospholipids
  • Tyrosine 3-Monooxygenase
  • Protein Kinase C
  • Phospholipases A
  • Phospholipases A2
  • Calcium