Lipids and proteins were found to contact a nascent type II membrane protein, as well as a nascent secretory protein, during their insertion into the membrane of the endoplasmic reticulum. This suggests that the protein-conducting channel is open laterally toward the lipid bilayer during an early stage of protein insertion. Contact to lipids was confined to the hydrophobic core region of the respective signal or signal anchor sequence. Thus, the nascent polypeptide is positioned in the translocation complex such that the signal or signal anchor sequence faces the lipid bilayer, whereas the hydrophilic, translocating portion is in proteinaceous environment
Secreted and integral membrane proteins compose up to one-third of the biological proteome. These pr...
AbstractAs summarized in this minireview, two different signal recognition events, one involving SRP...
A chemically charged amber suppressor tRNA was used to introduce the photoactivatable amino acid (Tm...
AbstractLipids and proteins were found to contact a nascent type II membrane protein, as well as a n...
Lipids and proteins were found to contact a nascent type II membrane protein, as well as a nascent s...
AbstractAs proteins are integrated into the membrane of the endoplasmic reticulum, some hydrophilic ...
AbstractWe have analyzed early phases of the cotranslational transport of the secretory protein prep...
AbstractWe have investigated how the transmembrane (TM) domain of a membrane protein is cotranslatio...
Most eukaryotic membrane proteins are cotranslationally integrated into the endoplasmic reticulum me...
AbstractPhotocrosslinking has been used to identify integral proteins of the endoplasmic reticulum m...
The immediate environment of nascent membrane proteins undergoing integration into the ER membrane w...
A chemically charged amber suppressor tRNA was used to introduce the photoactivatable amino acid (Tm...
We have used the homobifunctional cross-linking reagent disuccinimidyl suberate (DSS) to identify pr...
Phospholipids are synthesized at the endoplasmic reticulum (ER), the largest membrane bound organell...
Photocrosslinking has been used to identify integral proteins of the endoplasmic reticulum membrane ...
Secreted and integral membrane proteins compose up to one-third of the biological proteome. These pr...
AbstractAs summarized in this minireview, two different signal recognition events, one involving SRP...
A chemically charged amber suppressor tRNA was used to introduce the photoactivatable amino acid (Tm...
AbstractLipids and proteins were found to contact a nascent type II membrane protein, as well as a n...
Lipids and proteins were found to contact a nascent type II membrane protein, as well as a nascent s...
AbstractAs proteins are integrated into the membrane of the endoplasmic reticulum, some hydrophilic ...
AbstractWe have analyzed early phases of the cotranslational transport of the secretory protein prep...
AbstractWe have investigated how the transmembrane (TM) domain of a membrane protein is cotranslatio...
Most eukaryotic membrane proteins are cotranslationally integrated into the endoplasmic reticulum me...
AbstractPhotocrosslinking has been used to identify integral proteins of the endoplasmic reticulum m...
The immediate environment of nascent membrane proteins undergoing integration into the ER membrane w...
A chemically charged amber suppressor tRNA was used to introduce the photoactivatable amino acid (Tm...
We have used the homobifunctional cross-linking reagent disuccinimidyl suberate (DSS) to identify pr...
Phospholipids are synthesized at the endoplasmic reticulum (ER), the largest membrane bound organell...
Photocrosslinking has been used to identify integral proteins of the endoplasmic reticulum membrane ...
Secreted and integral membrane proteins compose up to one-third of the biological proteome. These pr...
AbstractAs summarized in this minireview, two different signal recognition events, one involving SRP...
A chemically charged amber suppressor tRNA was used to introduce the photoactivatable amino acid (Tm...