International audienceThe heterotrimeric Sec61 protein complex forms the functional core of the so-called translocon that forms an aqueous channel in the endoplasmic reticulum (ER). The primary role of the Sec61 complex is to allow protein import in the ER during translation. Surprisingly, a completely different function in intracellular Ca 2+ homeostasis has emerged for the Sec61 complex, and the latter is now accepted as one of the major Ca 2+ -leak pathways of the ER. In this review, we first discuss the structure of the Sec61 complex and focus on the pharmacology and regulation of the Sec61 complex as a Ca 2+ -leak channel. Subsequently, we will pay particular attention to pathologies that are linked to Sec61 mutations, such as plasma c...
The rough endoplasmic reticulum (ER) of nucleated human cells has crucial functions in protein biog...
Sec61p is the channel-forming subunit of the heterotrimeric Sec61 complex that mediates co-translati...
Ca2+ Leak Channels in the ER Membrane and their Regulatory Mechanisms. J. Vis. Exp. (53), e2730, doi...
The membrane of the endoplasmic reticulum (ER) of nucleated human cells harbors the protein transloc...
The rough endoplasmic reticulum (ER) of nucleated human cells has crucial functions in protein bioge...
The membrane of the endoplasmic reticulum (ER) of nucleated human cells harbors the protein transloc...
Contains fulltext : 235606.pdf (Publisher’s version ) (Open Access)The rough endop...
The endoplasmic reticulum (ER) is a major site for protein biosynthesis, required for production of ...
Most secreted and membrane proteins are targeted to and translocated across the endoplasmic reticulu...
The endoplasmic reticulum (ER) is the entry point to the secretory pathway and major site of protein...
The membrane of the endoplasmic reticulum (ER) in human cells harbors the protein translocon, which ...
Summary: Protein transport into the mammalian endoplasmic reticulum (ER) is mediated by the heterotr...
The endoplasmic reticulum (ER) is a site of protein biogenesis in eukaryotic cells. Perturbing ER ho...
In mammalian cells, signal peptide-dependent protein transport into the endoplasmic reticulum (ER) i...
The endoplasmic reticulum (ER) is a site of protein biogenesis in eukaryotic cells. Perturbing ER ho...
The rough endoplasmic reticulum (ER) of nucleated human cells has crucial functions in protein biog...
Sec61p is the channel-forming subunit of the heterotrimeric Sec61 complex that mediates co-translati...
Ca2+ Leak Channels in the ER Membrane and their Regulatory Mechanisms. J. Vis. Exp. (53), e2730, doi...
The membrane of the endoplasmic reticulum (ER) of nucleated human cells harbors the protein transloc...
The rough endoplasmic reticulum (ER) of nucleated human cells has crucial functions in protein bioge...
The membrane of the endoplasmic reticulum (ER) of nucleated human cells harbors the protein transloc...
Contains fulltext : 235606.pdf (Publisher’s version ) (Open Access)The rough endop...
The endoplasmic reticulum (ER) is a major site for protein biosynthesis, required for production of ...
Most secreted and membrane proteins are targeted to and translocated across the endoplasmic reticulu...
The endoplasmic reticulum (ER) is the entry point to the secretory pathway and major site of protein...
The membrane of the endoplasmic reticulum (ER) in human cells harbors the protein translocon, which ...
Summary: Protein transport into the mammalian endoplasmic reticulum (ER) is mediated by the heterotr...
The endoplasmic reticulum (ER) is a site of protein biogenesis in eukaryotic cells. Perturbing ER ho...
In mammalian cells, signal peptide-dependent protein transport into the endoplasmic reticulum (ER) i...
The endoplasmic reticulum (ER) is a site of protein biogenesis in eukaryotic cells. Perturbing ER ho...
The rough endoplasmic reticulum (ER) of nucleated human cells has crucial functions in protein biog...
Sec61p is the channel-forming subunit of the heterotrimeric Sec61 complex that mediates co-translati...
Ca2+ Leak Channels in the ER Membrane and their Regulatory Mechanisms. J. Vis. Exp. (53), e2730, doi...