Functional domains of the fatty acid transport proteins: Studies using protein chimeras

Concetta C. DiRusso, Dina Darwis, Thomas Obermeyer, Paul N. Black

Research output: Contribution to journalArticle

28 Citations (Scopus)

Abstract

Fatty acid transport proteins (FATP) function in fatty acid trafficking pathways, several of which have been shown to participate in the transport of exogenous fatty acids into the cell. Members of this protein family also function as acyl CoA synthetases with specificity towards very long chain fatty acids or bile acids. These proteins have two identifying sequence motifs: The ATP/AMP motif, an approximately 100 amino acid segment required for ATP binding and common to members of the adenylate-forming super family of proteins, and the FATP/VLACS motif that consists of approximately 50 amino acid residues and is restricted to members of the FATP family. This latter motif has been implicated in fatty acid transport in the yeast FATP orthologue Fat1p. In the present studies using a yeast strain containing deletions in FAT1 (encoding Fat1p) and FAA1 (encoding the major acyl CoA synthetase (Acsl) Faa1p) as an experimental platform, the phenotypic and functional properties of specific murine FATP1-FATP4 and FATP6-FATP4 protein chimeras were evaluated in order to define elements within these proteins that further distinguish the fatty acid transport and activation functions. As expected from previous work FATP1 and FATP4 were functional in the fatty acid transport pathway, while and FATP6 was not. All three isoforms were able to activate the very long chain fatty acids arachidonate (C20:4) and lignocerate (C24:0), but with distinguishing activities between saturated and highly unsaturated ligands. A 73 amino acid segment common to FATP1 and FATP4 and between the ATP/AMP and FATP/VLACS motifs was identified by studying the chimeras, which is hypothesized to contribute to the transport function.

Original languageEnglish (US)
Pages (from-to)135-143
Number of pages9
JournalBiochimica et Biophysica Acta - Molecular and Cell Biology of Lipids
Volume1781
Issue number3
DOIs
StatePublished - Mar 1 2008

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Fatty Acid Transport Proteins
Fatty Acids
Coenzyme A Ligases
Proteins
Amino Acid Motifs
Adenosine Triphosphate
Adenosine Monophosphate
Amino Acids
Yeasts
Bile Acids and Salts
Protein Isoforms
Ligands

Keywords

  • Activation
  • FATP
  • Protein chimera
  • Transport

ASJC Scopus subject areas

  • Molecular Biology
  • Cell Biology

Cite this

Functional domains of the fatty acid transport proteins : Studies using protein chimeras. / DiRusso, Concetta C.; Darwis, Dina; Obermeyer, Thomas; Black, Paul N.

In: Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids, Vol. 1781, No. 3, 01.03.2008, p. 135-143.

Research output: Contribution to journalArticle

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