AbstractAs proteins are integrated into the membrane of the endoplasmic reticulum, some hydrophilic polypeptide segments are transported through the translocation channel, others remain in the cytosol, and hydrophobic transmembrane sequences are released into the lipid phase. We have addressed the molecular mechanism by which these events occur. We demonstrate that both the lumenal and the cytosolic domains of a membrane protein are synthesized while the ribosome is membrane bound, so that even cytosolic domains come in contact with the translocation channel. We also find that, before translation of the protein is terminated, transmembrane sequences can laterally exit the translocation channel and enter the lipid environment. These results ...
Membrane proteins comprise around 20-30% of most proteomes. They play important roles in most bioche...
AbstractLipids and proteins were found to contact a nascent type II membrane protein, as well as a n...
In membrane biogenesis and protein targeting, polypeptide chains very often insert into and move acr...
AbstractAs proteins are integrated into the membrane of the endoplasmic reticulum, some hydrophilic ...
AbstractWe have investigated how the transmembrane (TM) domain of a membrane protein is cotranslatio...
AbstractDuring the cotranslational integration of a nascent protein into the endoplasmic reticulum m...
Most eukaryotic membrane proteins are cotranslationally integrated into the endoplasmic reticulum me...
AbstractThe initial steps in the biogenesis of membrane proteins parallel that of secretory proteins...
Most membrane proteins are composed of hydrophobic α-helical transmembrane segments and are integrat...
Membrane-spanning proteins have many crucial roles in the cell. New findings challenge our current u...
Most integral membrane proteins are targeted, inserted and assembled in the endoplasmic reticulum (E...
The biogenesis, folding, and structure of α-helical membrane proteins (MPs) are important to underst...
Most integral membrane proteins located within the endomembrane system of eukaryotic cells are first...
Lipids and proteins were found to contact a nascent type II membrane protein, as well as a nascent s...
Integral membrane proteins are cotranslationally inserted into the endoplasmic reticulum via the pro...
Membrane proteins comprise around 20-30% of most proteomes. They play important roles in most bioche...
AbstractLipids and proteins were found to contact a nascent type II membrane protein, as well as a n...
In membrane biogenesis and protein targeting, polypeptide chains very often insert into and move acr...
AbstractAs proteins are integrated into the membrane of the endoplasmic reticulum, some hydrophilic ...
AbstractWe have investigated how the transmembrane (TM) domain of a membrane protein is cotranslatio...
AbstractDuring the cotranslational integration of a nascent protein into the endoplasmic reticulum m...
Most eukaryotic membrane proteins are cotranslationally integrated into the endoplasmic reticulum me...
AbstractThe initial steps in the biogenesis of membrane proteins parallel that of secretory proteins...
Most membrane proteins are composed of hydrophobic α-helical transmembrane segments and are integrat...
Membrane-spanning proteins have many crucial roles in the cell. New findings challenge our current u...
Most integral membrane proteins are targeted, inserted and assembled in the endoplasmic reticulum (E...
The biogenesis, folding, and structure of α-helical membrane proteins (MPs) are important to underst...
Most integral membrane proteins located within the endomembrane system of eukaryotic cells are first...
Lipids and proteins were found to contact a nascent type II membrane protein, as well as a nascent s...
Integral membrane proteins are cotranslationally inserted into the endoplasmic reticulum via the pro...
Membrane proteins comprise around 20-30% of most proteomes. They play important roles in most bioche...
AbstractLipids and proteins were found to contact a nascent type II membrane protein, as well as a n...
In membrane biogenesis and protein targeting, polypeptide chains very often insert into and move acr...