The role of palmitoylation and transmembrane domain in sorting of transmembrane adaptor proteins
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
26585312
DOI
10.1242/jcs.175190
PII: jcs.175190
Knihovny.cz E-zdroje
- Klíčová slova
- LAT, PAG, Palmitoylation, Plasma membrane, Protein sorting, Transmembrane domain,
- MeSH
- adaptorové proteiny signální transdukční chemie metabolismus MeSH
- buněčná membrána metabolismus MeSH
- extracelulární prostor chemie MeSH
- glykosylace MeSH
- HEK293 buňky MeSH
- HeLa buňky MeSH
- Jurkat buňky MeSH
- lidé MeSH
- lipoylace * MeSH
- membránové proteiny chemie metabolismus MeSH
- terciární struktura proteinů MeSH
- transport proteinů MeSH
- vztahy mezi strukturou a aktivitou MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- adaptorové proteiny signální transdukční MeSH
- membránové proteiny MeSH
Plasma membrane proteins synthesised at the endoplasmic reticulum are delivered to the cell surface via sorting pathways. Hydrophobic mismatch theory based on the length of the transmembrane domain (TMD) dominates discussion about determinants required for protein sorting to the plasma membrane. Transmembrane adaptor proteins (TRAP) are involved in signalling events which take place at the plasma membrane. Members of this protein family have TMDs of varying length. We were interested in whether palmitoylation or other motifs contribute to the effective sorting of TRAP proteins. We found that palmitoylation is essential for some, but not all, TRAP proteins independent of their TMD length. We also provide evidence that palmitoylation and proximal sequences can modulate sorting of artificial proteins with TMDs of suboptimal length. Our observations point to a unique character of each TMD defined by its primary amino acid sequence and its impact on membrane protein localisation. We conclude that, in addition to the TMD length, secondary sorting determinants such as palmitoylation or flanking sequences have evolved for the localisation of membrane proteins.
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