Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.814544
Title: Mechanisms of multipass membrane protein biogenesis
Author: Chitwood, Patrick
ISNI:       0000 0004 9354 2027
Awarding Body: University of Cambridge
Current Institution: University of Cambridge
Date of Award: 2020
Availability of Full Text:
Access from EThOS:
Full text unavailable from EThOS. Please try the link below.
Access from Institution:
Abstract:
A crucial aspect of cellular physiology is the ability of a single cell to remain autonomous and concentrate reagents to improve efficiency. Semi-permeable membranes facilitate autonomy via an outer barrier (plasma membrane) and enclose functional hubs (organelles) to efficiently carry out biological processes. However, cells do not live in isolation and must communicate with neighboring cells, uptake and traffic nutrients, and react to a dynamic extracellular environment. All these processes require integral membrane proteins (IMPs), which are embedded within all cellular membranes. Highlighting their importance is a myriad of human diseases observed upon disruption of their biogenesis. This thesis aims to describe our recent contributions to the understanding of how membrane proteins are made at the endoplasmic reticulum (ER), the primary site of IMP biogenesis in the cell. Although IMPs are defined by a single feature, a transmembrane domain (TMD), the ~5000 encoded in the mammalian genome are diverse. While some contain a single TMD, most feature many biophysically unique TMDs. Productive bio- genesis of most “multipass” membrane proteins requires insertion in a defined topology as well as packing of their TMDs into a helical bundle, often through inter- actions between polar residues unstably located in the hydrophobic lipid bilayer. Neither the mechanisms that facilitate accurate topological insertion or the subsequent stabilization of polar TMDs during IMP biogenesis are completely understood. First, we demonstrate the efficient topogenesis of many GPCRs requires the conserved ER membrane protein complex (EMC). This is supported by biochemical reconstitution of β1-adrenergic receptor (β1AR) insertion in-vitro, which placed EMC at an early step during co-translational insertion of the first TMD (TMD1). In the absence of EMC, TMD1 was topologically inverted or failed to insert altogether. EMC and SRP receptor were sufficient for the correct insertion of TMD1, while insertion of the next TMD required Sec61. Finally, EMC necessity could be by- passed by enforcement of TMD1 topology via an N-terminal signal peptide. Following accurate insertion of TMD1, we define the engagement of a newly identified intramembrane chaperone protein complex that we term the PAT complex. The PAT complex is an obligate heterodimer consisting of the highly conserved proteins CCDC47 and Asterix. A diverse set of multipass membrane proteins show impaired biogenesis upon PAT complex depletion, despite correct topological insertion. Bio- chemical analyses demonstrate PAT complex engages nascent TMDs that contain unshielded polar amino acids but disengages upon substrate folding. Thus, EMC cooperates with Sec61 to co-translationally insert TMDs, ensuring accurate membrane protein topogenesis, while the PAT complex acts after insertion to protect transmembrane domains during their assembly.
Supervisor: Hegde, Ramanujan Sponsor: Cambridge Trust ; MRC
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.814544  DOI:
Keywords: Endoplasmic Reticulum ; G-Protein Coupled Receptor ; GPCR ; Membrane ; Multipass membrane proteins ; Polytopic membrane protein ; Chaperone ; Intramembrane chaperone ; transmembrane domain ; TMD ; Membrane insertion ; cotranslational ; ER membrane protein complex ; EMC ; PAT complex ; CCDC47 ; Asterix ; Biochemistry ; Translation ; Ribosome
Share: