Literature DB >> 8707845

Lipid-modified, cysteinyl-containing peptides of diverse structures are efficiently S-acylated at the plasma membrane of mammalian cells.

H Schroeder1, R Leventis, S Shahinian, P A Walton, J R Silvius.   

Abstract

A variety of cysteine-containing, lipid-modified peptides are found to be S-acylated by cultured mammalian cells. The acylation reaction is highly specific for cysteinyl over serinyl residues and for lipid-modified peptides over hydrophilic peptides. The S-acylation process appears by various criteria to be enzymatic and resembles the S-acylation of plasma membrane-associated proteins in various characteristics, including inhibition by tunicamycin. The substrate range of the S-acylation reaction encompasses, but is not limited to, lipopeptides incorporating the motifs myristoylGC- and -CXC(farnesyl)-OCH3, which are reversibly S-acylated in various intracellular proteins. Mass-spectrometric analysis indicates that palmitoyl residues constitute the predominant but not the only type of S-acyl group coupled to a lipopeptide carrying the myristoylGC- motif, with smaller amounts of S-stearoyl and S-oleoyl substituents also detectable. Fluorescence microscopy using NBD-labeled cysteinyl lipopeptides reveals that the products of lipopeptide S-acylation, which cannot diffuse between membranes, are in almost all cases localized preferentially to the plasma membrane. This preferential localization is found even at reduced temperatures where vesicular transport from the Golgi complex to the plasma membrane is suppressed, strongly suggesting that the plasma membrane itself is the preferred site of S-acylation of these species. Uniquely among the lipopeptides studied, species incorporating an unphysiological N-myristoylcysteinyl- motif also show substantial formation of S-acylated products in a second, intracellular compartment identified as the Golgi complex by its labeling with a fluorescent ceramide. Our results suggest that distinct S-acyltransferases exist in the Golgi complex and plasma membrane compartments and that S-acylation of motifs such as myristoylGC- occurs specifically at the plasma membrane, affording efficient targeting of cellular proteins bearing such motifs to this membrane compartment.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8707845      PMCID: PMC2120939          DOI: 10.1083/jcb.134.3.647

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  89 in total

1.  Lipid modifications of G proteins: alpha subunits are palmitoylated.

Authors:  M E Linder; P Middleton; J R Hepler; R Taussig; A G Gilman; S M Mumby
Journal:  Proc Natl Acad Sci U S A       Date:  1993-04-15       Impact factor: 11.205

2.  A novel N-terminal motif for palmitoylation of G-protein alpha subunits.

Authors:  M Parenti; M A Viganó; C M Newman; G Milligan; A I Magee
Journal:  Biochem J       Date:  1993-04-15       Impact factor: 3.857

3.  P-selectin is acylated with palmitic acid and stearic acid at cysteine 766 through a thioester linkage.

Authors:  T Fujimoto; E Stroud; R E Whatley; S M Prescott; L Muszbek; M Laposata; R P McEver
Journal:  J Biol Chem       Date:  1993-05-25       Impact factor: 5.157

4.  Proteolipid protein (PLP) of CNS myelin: positions of free, disulfide-bonded, and fatty acid thioester-linked cysteine residues and implications for the membrane topology of PLP.

Authors:  T Weimbs; W Stoffel
Journal:  Biochemistry       Date:  1992-12-15       Impact factor: 3.162

5.  Reversible palmitoylation of the protein-tyrosine kinase p56lck.

Authors:  L A Paige; M J Nadler; M L Harrison; J M Cassady; R L Geahlen
Journal:  J Biol Chem       Date:  1993-04-25       Impact factor: 5.157

6.  Agonist-modulated palmitoylation of beta 2-adrenergic receptor in Sf9 cells.

Authors:  B Mouillac; M Caron; H Bonin; M Dennis; M Bouvier
Journal:  J Biol Chem       Date:  1992-10-25       Impact factor: 5.157

7.  The G protein alpha s subunit incorporates [3H]palmitic acid and mutation of cysteine-3 prevents this modification.

Authors:  M Y Degtyarev; A M Spiegel; T L Jones
Journal:  Biochemistry       Date:  1993-08-17       Impact factor: 3.162

8.  Interaction of acyl-CoA binding protein (ACBP) on processes for which acyl-CoA is a substrate, product or inhibitor.

Authors:  J T Rasmussen; J Rosendal; J Knudsen
Journal:  Biochem J       Date:  1993-06-15       Impact factor: 3.857

9.  Palmitylation of neuromodulin (GAP-43) is not required for phosphorylation by protein kinase C.

Authors:  E R Chapman; R P Estep; D R Storm
Journal:  J Biol Chem       Date:  1992-12-15       Impact factor: 5.157

10.  Immunocytochemical analysis of the transfer of vesicular stomatitis virus G glycoprotein from the intermediate compartment to the Golgi complex.

Authors:  L V Lotti; M R Torrisi; M C Pascale; S Bonatti
Journal:  J Cell Biol       Date:  1992-07       Impact factor: 10.539

View more
  17 in total

1.  Functional roles for fatty acylated amino-terminal domains in subcellular localization.

Authors:  J B McCabe; L G Berthiaume
Journal:  Mol Biol Cell       Date:  1999-11       Impact factor: 4.138

2.  Localization of a peripheral membrane protein: Gbetagamma targets Galpha(Z).

Authors:  C S Fishburn; S K Pollitt; H R Bourne
Journal:  Proc Natl Acad Sci U S A       Date:  2000-02-01       Impact factor: 11.205

3.  Association of prenylated proteins with the plasma membrane and the inner nuclear membrane is mediated by the same membrane-targeting motifs.

Authors:  H Hofemeister; K Weber; R Stick
Journal:  Mol Biol Cell       Date:  2000-09       Impact factor: 4.138

4.  DHHC20: a human palmitoyl acyltransferase that causes cellular transformation.

Authors:  Jeremiah M Draper; Charles D Smith
Journal:  Mol Membr Biol       Date:  2010-04       Impact factor: 2.857

5.  Palmitoylation of p59fyn is reversible and sufficient for plasma membrane association.

Authors:  A Wolven; H Okamura; Y Rosenblatt; M D Resh
Journal:  Mol Biol Cell       Date:  1997-06       Impact factor: 4.138

6.  Cellular palmitoylation and trafficking of lipidated peptides.

Authors:  Jeremiah M Draper; Zuping Xia; Charles D Smith
Journal:  J Lipid Res       Date:  2007-05-24       Impact factor: 5.922

Review 7.  Exploring protein lipidation with chemical biology.

Authors:  Howard C Hang; Maurine E Linder
Journal:  Chem Rev       Date:  2011-09-16       Impact factor: 60.622

8.  Pseudo-enzymatic S-acylation of a myristoylated yes protein tyrosine kinase peptide in vitro may reflect non-enzymatic S-acylation in vivo.

Authors:  M C Bañó; C S Jackson; A I Magee
Journal:  Biochem J       Date:  1998-03-01       Impact factor: 3.857

9.  Plasma membrane localization of G alpha z requires two signals.

Authors:  J Morales; C S Fishburn; P T Wilson; H R Bourne
Journal:  Mol Biol Cell       Date:  1998-01       Impact factor: 4.138

10.  DHHC protein S-acyltransferases use similar ping-pong kinetic mechanisms but display different acyl-CoA specificities.

Authors:  Benjamin C Jennings; Maurine E Linder
Journal:  J Biol Chem       Date:  2012-01-13       Impact factor: 5.157

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.