Nearly 30% of the eukaryotic genome encodes integral membrane proteins, which serve many essential functions as receptors, enzymes, anchors and transporters. Membrane proteins of the cell surface and most intracellular compartments are ?rst assembled at the endoplasmic reticulum (ER). These proteins are cotranslationally targeted to the ER by the signal recognition particle and inserted into the bilayer by the Sec61 complex. In the simplest view, the core Sec61 complex mediates insertion by guiding nascent hydrophobic transmembrane domains (TMDs) into a central, aqueous pore which opens laterally to allow TMD entry into the bilayer. While this model has proven valuable for understanding the basic mechanism of TMD insertion, its application to the biogenesis of physiologic substrates?especially those with multiple TMDs?has been challenging. This challenge arises from the extreme diversity of eukaryotic membrane proteins, which have drastically different topologies and biophysical requirements for insertion, folding, modi?cation and assembly into functional entities. These different steps are coordinated by the `translocon', a poorly de?ned and dynamic ensemble comprising the Sec61 complex in association with a variety of accessory subunits. The structures, stoichiometry and functions of most of this machinery are poorly understood, and their roles in membrane protein biogenesis are largely unexplored. Understanding how different translocon complexes mediate membrane biogenesis is a fundamental question in cell biology We recently classi?ed a conserved but poorly understood human protein called TMCO1 as a member of a previously unrecognized superfamily of proteins involved in membrane protein biogenesis. Consistent with this assignment, our preliminary data demonstrate that TMCO1 is part of a multi-component assembly that includes the Sec61 complex and ribosomes, and directly link it to a role in the cotranslational insertion, folding and/or assembly of a large group of membrane proteins. Here we build on this conceptual and technical foundation to de?ne how TMCO1 functions in membrane protein biogenesis.
In Aim 1, we will globally identify the set of nascent TMCO1 substrates and use these to de?ne the mechanism of TMCO1 action.
In Aim 2, we will rigorously analyze the interaction partners of TMCO1 and de?ne the structure of TMCO1-containing ribosome-Sec61 complexes. We will do this using a multi-disciplinary approach that combines biochemical, genetic and structural analyses.

Public Health Relevance

Eukaryotic cells encode thousands of different membrane proteins that are essential for growth and survival. We have discovered a new pathway that directs the biogenesis of hundreds of newly synthesized membrane proteins at the endoplasmic reticulum membrane. De?ning how the cellular machinery coordinates this process is essential to understand how healthy cells function, and may enable the development of new therapies in the ?ght against human diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM130051-02
Application #
9735320
Study Section
Nuclear and Cytoplasmic Structure/Function and Dynamics Study Section (NCSD)
Program Officer
Flicker, Paula F
Project Start
2018-07-01
Project End
2022-06-30
Budget Start
2019-07-01
Budget End
2020-06-30
Support Year
2
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Chicago
Department
Type
Schools of Arts and Sciences
DUNS #
005421136
City
Chicago
State
IL
Country
United States
Zip Code
60637