Deutsch
 
Hilfe Datenschutzhinweis Impressum
  DetailsucheBrowse

Datensatz

DATENSATZ AKTIONENEXPORT
  Structure of tetrameric forms of the serotonin-gated 5-HT3A receptor ion channel

Introini, B., Cui, W., Chu, X., Zhang, Y., Alves, A. C., Eckhardt-Strelau, L., et al. (2024). Structure of tetrameric forms of the serotonin-gated 5-HT3A receptor ion channel. The EMBO Journal, 43(20), 4451-4471. doi:10.1038/s44318-024-00191-5.

Item is

Basisdaten

einblenden: ausblenden:
Genre: Zeitschriftenartikel

Dateien

einblenden: Dateien
ausblenden: Dateien
:
introini-et-al-2024-structure-of-tetrameric-forms-of-the-serotonin-gated-5-ht3a-receptor-ion-channel.pdf (beliebiger Volltext), 8MB
Name:
introini-et-al-2024-structure-of-tetrameric-forms-of-the-serotonin-gated-5-ht3a-receptor-ion-channel.pdf
Beschreibung:
-
OA-Status:
Keine Angabe
Sichtbarkeit:
Öffentlich
MIME-Typ / Prüfsumme:
application/pdf / [MD5]
Technische Metadaten:
Copyright Datum:
-
Copyright Info:
-
Lizenz:
-

Externe Referenzen

einblenden:

Urheber

einblenden:
ausblenden:
 Urheber:
Introini, Bianca1, 2, Autor                 
Cui, Wenqiang3, 4, Autor
Chu, Xiaofeng5, Autor
Zhang, Yingyi1, 2, Autor           
Alves, Ana Catarina6, Autor
Eckhardt-Strelau, Luise1, Autor           
Golusik, Sabrina5, Autor
Tol, Menno6, Autor
Vogel, Horst3, 6, 7, Autor
Yuan, Shuguang3, 8, Autor
Kudryashev, Mikhail1, 2, 5, 9, Autor                 
Affiliations:
1Sofja Kovalevskaja Group, Max Planck Institute of Biophysics, Max Planck Society, ou_2253651              
2Buchmann Institute for Molecular Life Sciences (BMLS), Goethe University of Frankfurt am Main, Frankfurt on Main, Germany, ou_persistent22              
3The Research Center for Computer-aided Drug Discovery, Institute of Biomedicine and Biotechnology, The Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences Shenzhen, China, ou_persistent22              
4University of Chinese Academy of Sciences, Beijing, China, ou_persistent22              
5Max-Delbrück-Center for Molecular Medicine in the Helmholtz Association (MDC), In Situ Structural Biology, Berlin, Germany, ou_persistent22              
6Institute of Chemical Sciences and Engineering (ISIC), Ecole Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland, ou_persistent22              
7Faculty of Pharmaceutical Sciences, Shenzhen University of Advanced Technology (SUAT), Shenzhen, China, ou_persistent22              
8AlphaMol Science Ltd, Shenzhen, China, ou_persistent22              
9Institute of Medical Physics and Biophysics, Charité-Universitätsmedizin, Berlin, Germany, ou_persistent22              

Inhalt

einblenden:
ausblenden:
Schlagwörter: Cryo-EM, Ion Channels, Pentameric Ligand-gated Ion Channels, Serotonin Receptors
 Zusammenfassung: Multimeric membrane proteins are produced in the endoplasmic reticulum and transported to their target membranes which, for ion channels, is typically the plasma membrane. Despite the availability of many fully assembled channel structures, our understanding of assembly intermediates, multimer assembly mechanisms, and potential functions of non-standard assemblies is limited. We demonstrate that the pentameric ligand-gated serotonin 5-HT3A receptor (5-HT3AR) can assemble to tetrameric forms and report the structures of the tetramers in plasma membranes of cell-derived microvesicles and in membrane memetics using cryo-electron microscopy and tomography. The tetrameric structures have near-symmetric transmembrane domains, and asymmetric extracellular domains, and can bind serotonin molecules. Computer simulations, based on our cryo-EM structures, were used to decipher the assembly pathway of pentameric 5-HT3R and suggest a potential functional role for the tetrameric receptors.

Details

einblenden:
ausblenden:
Sprache(n): eng - English
 Datum: 2024-06-162024-03-192024-07-152024-09-042024-10
 Publikationsstatus: Erschienen
 Seiten: 21
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: DOI: 10.1038/s44318-024-00191-5
BibTex Citekey: introini_structure_2024
 Art des Abschluß: -

Veranstaltung

einblenden:

Entscheidung

einblenden:

Projektinformation

einblenden:

Quelle 1

einblenden:
ausblenden:
Titel: The EMBO Journal
  Andere : EMBO J.
Genre der Quelle: Zeitschrift
 Urheber:
Affiliations:
Ort, Verlag, Ausgabe: Nature Publishing Group
Seiten: - Band / Heft: 43 (20) Artikelnummer: - Start- / Endseite: 4451 - 4471 Identifikator: ISSN: 0261-4189
CoNE: https://pure.mpg.de/cone/journals/resource/954925497061_1