Mechanisms of ER Protein Import

• Autore: Zimmermann Richard
• Pubblicazione: Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
• Descrizione fisica: 1 electronic resource (258 p.)
• Soggetto topico: Research & information: general; Biology, life sciences
• Soggetto non controllato: chaperones; contact sites; endoplasmic reticulum; ER-SURF; membrane extraction; mitochondria; protein targeting; bimolecular luminescence complementation; competition; split luciferase; membrane proteins; protein-protein interactions; Sec61 complex; Sec63; synthetic peptide complementation; TRAP complex; ER protein translocase; signal peptide; protein translocation; nascent peptide chain; membrane insertion; molecular modelling; molecular dynamics simulations; molecular docking; signal peptidase; ER translocon; signal recognition particle dependent protein targeting; Sec61 dependent translocation; co-translational translocation; inhibitor; high throughput screening; Sec61; Sec62; folding; insertion; membrane protein; translocon; ribosome; transmembrane segment; lipid droplets; peroxisomes; PEX3; membrane protein insertion; label-free quantitative mass spectrometry; differential protein abundance analysis; Zellweger syndrome; GET; protein transport; SND; SRP; EMC; positive-inside rule; hydrophobicity; transmembrane helix; signal recognition particle; nascent polypeptide-associated complex; fidelity; cyclotriazadisulfonamide; ER quality control; DNAJC3; preprotein; Sec61 translocon; ribosome stalling; signal sequence; Sec61 translocase; NAC
• Persona (resp. second.): LangSven; ZimmermannRichard
• Sommario/riassunto: Protein import into the endoplasmic reticulum (ER) is the first step in the biogenesis of approximately 10,000 different soluble and membrane proteins of human cells, which amounts to about 30% of the proteome. Most of these proteins fulfill their functions either in the membrane or lumen of the ER plus the nuclear envelope, in one of the organelles of the pathways for endo- and exocytosis (ERGIC, Golgi apparatus, endosome, lysosome, and trafficking vesicles), or at the cell surface as plasma membrane or secreted proteins. An increasing number of membrane proteins destined to lipid droplets, peroxisomes or mitochondria are first targeted to and inserted into the ER membrane prior to their integration into budding lipid droplets or peroxisomes or prior to their delivery to mitochondria via the ER-SURF pathway. ER protein import involves two stages, ER targeting, which guarantees membrane specificity, and the insertion of nascent membrane proteins into or translocation of soluble precursor polypeptides across the ER membrane. In most cases, both processes depend on amino-terminal signal peptides or transmembrane helices, which serve as signal peptide equivalents. However, the targeting reaction can also involve the ER targeting of specific mRNAs or ribosome–nascent chain complexes. Both processes may occur co- or post-translationally and are facilitated by various sophisticated machineries, which reside in the cytosol and the ER membrane, respectively. Except for resident ER and mitochondrial membrane proteins, the mature proteins are delivered to their functional locations by vesicular transport.
• Titolo autorizzato: Mechanisms of ER Protein Import
• Formato: Materiale a stampa
• Livello bibliografico: Monografia
• Lingua di pubblicazione: Inglese
• Record Nr.: 9910576886203321
• Lo trovi qui: Univ. Federico II