دورية أكاديمية

Control of AMPA receptor activity by the extracellular loops of auxiliary proteins

التفاصيل البيبلوغرافية
العنوان: Control of AMPA receptor activity by the extracellular loops of auxiliary proteins
المؤلفون: Riva, Irene, Eibl, Clarissa, Volkmer, Rudolf, Carbone, Anna Lisa, Plested, Andrew
المصدر: eLife, 6: e28680
سنة النشر: 2017
المجموعة: Publisso (ZB MED-Publikationsportal Lebenswissenschaften)
مصطلحات موضوعية: desensitization, none, receptor kinetics, modulation, biophysics, glutamate, neuroscience
الوصف: At synapses throughout the mammalian brain, AMPA receptors form complexes with auxiliary proteins, including TARPs. However, how TARPs modulate AMPA receptor gating remains poorly understood. We built structural models of TARP-AMPA receptor complexes for TARPs γ2 and γ8, combining recent structural studies and de novo structure predictions. These models, combined with peptide binding assays, provide evidence for multiple interactions between GluA2 and variable extracellular loops of TARPs. Substitutions and deletions of these loops had surprisingly rich effects on the kinetics of glutamate-activated currents, without any effect on assembly. Critically, by altering the two interacting loops of γ2 and γ8, we could entirely remove all allosteric modulation of GluA2, without affecting formation of AMPA receptor-TARP complexes. Likewise, substitutions in the linker domains of GluA2 completely removed any effect of γ2 on receptor kinetics, indicating a dominant role for this previously overlooked site proximal to the AMPA receptor channel gate.
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: https://repository.publisso.de/resource/frl:6406714Test; https://doi.org/10.7554/eLife.28680Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599240Test/
DOI: 10.7554/eLife.28680
الإتاحة: https://doi.org/10.7554/eLife.28680Test
https://repository.publisso.de/resource/frl:6406714Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599240Test/
حقوق: https://creativecommons.org/licenses/by/4.0Test/
رقم الانضمام: edsbas.859359E0
قاعدة البيانات: BASE