AbstractWe investigated the role of the stop transfer sequence of human UGT1A6 in ER assembly and enzyme activity. We found that this sequence was able to address and translocate the upstream lumenal domain into microsomal membranes in vitro co- and posttranslationally. The signal activity of this sequence was further demonstrated in HeLa cells by its ability to target and maintain the CD4 protein deleted from both the N-terminal signal peptide and C-terminal transmembrane domain into the ER. We showed that total or partial deletion of the stop transfer sequence of UGT1A6 severely impaired enzyme activity highlighting its importance in both membrane assembly and function
Bifunctional cross-linking reagents were used to probe the protein environment in the ER membrane of...
We have used the homobifunctional cross-linking reagent disuccinimidyl suberate (DSS) to identify pr...
To better define the mechanism of membrane protein insertion into the membrane of the endoplasmic re...
AbstractWe investigated the role of the stop transfer sequence of human UGT1A6 in ER assembly and en...
AbstractUDP-glucuronosyltransferase 1A6 (UGT1A6) is a membrane glycoprotein of the endoplasmic retic...
Many membrane proteins fold inefficiently and require the help of enzymes and chaperones. Here we re...
The signal sequence within polypeptide chains that designates whether a protein is to be anchored to...
The Sec61 translocon accommodates ER-targeted polypeptides including membrane proteins and secretory...
Using a photocross-linking approach we have investigated the cytosolic and membrane components invol...
AbstractWe have analyzed early phases of the cotranslational transport of the secretory protein prep...
AbstractThe role of the C-terminal region of the 74-kDa form of l-histidine decarboxylase (HDC) in t...
The immediate environment of nascent membrane proteins undergoing integration into the ER membrane w...
The metazoan Sec61 translocon transports polypeptides into and across the membrane of the endoplasmi...
Co-translational import into the endoplasmic reticulum (ER) is primarily controlled by N-terminal si...
A chemically charged amber suppressor tRNA was used to introduce the photoactivatable amino acid (Tm...
Bifunctional cross-linking reagents were used to probe the protein environment in the ER membrane of...
We have used the homobifunctional cross-linking reagent disuccinimidyl suberate (DSS) to identify pr...
To better define the mechanism of membrane protein insertion into the membrane of the endoplasmic re...
AbstractWe investigated the role of the stop transfer sequence of human UGT1A6 in ER assembly and en...
AbstractUDP-glucuronosyltransferase 1A6 (UGT1A6) is a membrane glycoprotein of the endoplasmic retic...
Many membrane proteins fold inefficiently and require the help of enzymes and chaperones. Here we re...
The signal sequence within polypeptide chains that designates whether a protein is to be anchored to...
The Sec61 translocon accommodates ER-targeted polypeptides including membrane proteins and secretory...
Using a photocross-linking approach we have investigated the cytosolic and membrane components invol...
AbstractWe have analyzed early phases of the cotranslational transport of the secretory protein prep...
AbstractThe role of the C-terminal region of the 74-kDa form of l-histidine decarboxylase (HDC) in t...
The immediate environment of nascent membrane proteins undergoing integration into the ER membrane w...
The metazoan Sec61 translocon transports polypeptides into and across the membrane of the endoplasmi...
Co-translational import into the endoplasmic reticulum (ER) is primarily controlled by N-terminal si...
A chemically charged amber suppressor tRNA was used to introduce the photoactivatable amino acid (Tm...
Bifunctional cross-linking reagents were used to probe the protein environment in the ER membrane of...
We have used the homobifunctional cross-linking reagent disuccinimidyl suberate (DSS) to identify pr...
To better define the mechanism of membrane protein insertion into the membrane of the endoplasmic re...