• Skip to primary navigation
  • Skip to main content
  • Skip to primary sidebar
MRC Laboratory of Molecular Biology

MRC Laboratory of Molecular Biology

One of the world's leading research institutes, our scientists are working to advance understanding of biological processes at the molecular level - providing the knowledge needed to solve key problems in human health.

  • Home
  • About LMB
  • Research
  • Research Groups
  • Students
  • Recruitment
  • Life at the LMB
  • Achievements
  • News & Events
Home > The molecular architecture of neurotransmission
nb

Radu Aricescu

The molecular architecture of neurotransmission

Group Leader Page

Chemical synapses are cellular connectors that define the organization and function of neuronal circuits and, as a result, the fundamental ability of the brain to acquire, process and store information. Two small molecules, glutamate (excitatory) and gamma-aminobutyric acid (GABA, inhibitory) mediate the majority of synaptic transmission in the vertebrate central nervous system. These bind ligand-gated ion channels and G-protein coupled receptors, to initiate neuronal signalling events.

The steady progress in the structural biology of membrane proteins during the past decade has provided a wealth of information on purified neurotransmitter receptors. We know how most of them look, and can imagine how they function. In a physiological context, however, these receptors do not work, or even exist, in isolation. They form merely the cores of large protein assemblies, including extracellular, transmembrane and intracellular molecules, which play essential roles throughout the "life-cycle" of synapses. A structure-based, mechanistic understanding of such assemblies is currently lacking.

Your project will focus on the structural and functional analysis of neurotransmitter receptor supra-molecular complexes. These span the synaptic cleft to physically connect neurotransmitter release sites in the pre-synaptic membrane with receptors on the post-synaptic side. Multiple options are available, built around the expertise available in our group on GABAA and glutamate ligand-gated ion channel families. Enquiries are encouraged, to discuss further details. This is an excellent opportunity to acquire experience in human membrane protein biochemistry and modern structural biology, including single-particle cryo-EM and cryo-electron tomography and plasma-FIB milling of brain tissue lamellae. Structural work will be combined with biophysical analyses, electrophysiology and super-resolution fluorescence microscopy. The LMB provides all the infrastructure required and an outstanding training environment for these techniques.

Our core group members (including the PI) have joint appointments in industry, which offers realistic insights and opportunities to translate academic discoveries into real-life therapies.


References

Sente, A., Desai, R., Naydenova, K., Malinauskas, T., Jounaidi, Y., Miehling, J., Zhou, X., Masiulis, S., Hardwick, S.W., Chirgadze, D.Y., Miller, K.W., Aricescu, A.R. (2022)
Differential assembly diversifies GABAA receptor structures and signalling
Nature 604(7904): 190-194

Suzuki, K., Elegheert, J., Song, I., Sasakura, H., Senkov, O., Matsuda, K., Kakegawa, W., Clayton, A.J., Chang, V.T., Ferrer-Ferrer, M., Miura, E., Kaushik, R., Ikeno, M., Morioka, Y., Takeuchi, Y., Shimada, T., Otsuka, S., Stoyanov, S., Watanabe, M., Takeuchi, K., Dityatev, A., Aricescu, A.R., Yuzaki, M. (2020)
A synthetic synaptic organizer protein restores glutamatergic neuronal circuits
Science 369(6507): eabb4853

Masiulis, S., Desai, R., Uchański, T., Martin, I.S., Laverty, D., Karia, D., Malinauskas, T., Zivanov, J., Pardon, E., Kotecha, A., Steyaert, J., Miller, K.W., Aricescu, A.R. (2019)
GABAA receptor signalling mechanisms revealed by structural pharmacology
Nature 565(7740): 454-459

Laverty, D., Desai, R., Uchański, T., Masiulis, S., Stec, W.J., Malinauskas, T., Zivanov, J., Pardon, E., Steyaert, J., Miller, K.W., Aricescu, A.R. (2019)
Cryo-EM structure of the human α1β3γ2 GABAA receptor in a lipid bilayer
Nature 565(7740): 516-520

Elegheert, J., Cvetkovska, V., Clayton, A.J., Heroven, C., Vennekens, K.M., Smukowski, S.N., Regan, M.C., Jia, W., Smith, A.C., Furukawa, H., Savas, J.N., Wit, J.d., Begbie, J., Craig, A.M., Aricescu, A.R. (2017)
Structural Mechanism for Modulation of Synaptic Neuroligin-Neurexin Signaling by MDGA Proteins
Neuron 95(4): 896-913

Elegheert, J., Kakegawa, W., Clay, J.E., Shanks, N.F., Behiels, E., Matsuda, K., Kohda, K., Miura, E., Rossmann, M., Mitakidis, N., Motohashi, J., Chang, V.T., Siebold, C., Greger, I.H., Nakagawa, T., Yuzaki, M., Aricescu, A.R. (2016)
Structural basis for integration of GluD receptors within synaptic organizer complexes
Science 353(6296): 295-9

Primary Sidebar

  • Home
  • About LMB
    • Useful Contacts
    • Building and Facilities
    • LMBees Blog
    • Fast Facts
    • History of the LMB
    • LMB Archive
      • Books
      • Manuscripts & Correspondence
      • Photographs
        • Browse the photo archive
      • Recordings
      • Newspaper Articles Archive
      • Scientific Models
      • Published Research
    • LMB Alumni
      • LMB Alumni List
      • LMB Alumni News
      • Newsletters
      • Share Your Memories
        • Gerry Rubin: Looking Back
        • Behind the Scenes with… Steve Scotcher
      • Photographs from the Archive
      • Keeping in touch
    • Max Perutz Fund
    • How to Find Us
    • Contact Directory
  • Research
    • Goals and Research Focus
    • Cell Biology
    • Neurobiology
      • Initiative with the Department of Clinical Neurosciences
    • Protein and Nucleic Acid Chemistry
      • Centre for Chemical and Synthetic Biology
    • Structural Studies
    • Technology Transfer
      • History Of Technology Transfer
      • Examples of Recent Technology Transfer Initiatives
    • Scientific Facilities & Support Services
    • Locally Developed Software
    • Scientific Training
      • Electron Microscopy
      • Biophysics Lectures
      • Macromolecular Crystallisation
      • Crystallography Course 2013
      • Statistics Course 2014
      • RNA-seq course 2020
    • Published Research
    • Molecular Immunity Unit
    • Animal Research
      • Why is animal research needed?
      • Alternatives to using Animals in Research
      • Welfare and ethics
      • LMB Research Involving Animals
      • Biological Services Group
      • Concordat on Openness in Animal Research
      • Useful Links
  • Research Groups
    • A to G
    • H to M
    • N to S
    • T to Z
    • Emeritus
    • LMB Fellows
    • Molecular Immunity Unit
  • Students
    • International PhD Programme
      • Programme Overview
      • Projects
      • Student Testimonials
      • Entrance Requirements
      • Overview of admissions
      • Funding
      • How To Apply
      • Key Dates for Applicants
      • FAQs
      • Useful Links
      • How did you hear about us?
      • Contact Us
    • Graduate Student Association
    • Student Placement Scheme
    • Work Experience
  • Recruitment
    • Current Vacancies
    • Postdoctoral Opportunities
    • Students
  • Life at the LMB
    • Working Here
    • LMBees Blog
    • Living Socially
    • Equality, Diversity and Inclusion (EDI)
    • Group Leader Profiles
  • Achievements
    • LMB Nobel Prizes
    • Royal Society Awards
    • EMBO Awards
    • Academy of Medical Sciences
    • Perutz Student Prize
    • Joan A. Steitz Postdoc Prize
    • Technology Transfer
  • News & Events
    • Insight on Research
    • LMB News
    • LMB In The News
    • LMB Alumni News
    • LMB 365
    • Newspaper Archive
    • Scientific Glossary
    • Scientific Seminars
    • Scientific Training
    • Public Engagement
      • Supporting Education
      • LMB on the Road
      • Events at the LMB
      • Resources
      • LMB Science Stories
      • Contact Us
    • Information for Journalists
    • Photographs

Search

  • Privacy & Cookies
  • Contact Directory
  • Freedom of Information
  • Site Map
Find Us
©2025 MRC Laboratory of Molecular Biology,
Francis Crick Avenue, Cambridge Biomedical Campus, Cambridge CB2 0QH, UK. 01223 267000

The MRC is part of UK Research and Innovation

Contact Us

This site uses cookies. The LMB may use cookies to analyse how you use our website. We use external analysis systems which may set additional cookies to perform their analysis. These cookies (and any others in use) are detailed in our Privacy and Cookies Policy and are integral to our website. You can delete or disable these cookies in your web browser if you wish, but then our site may not work as it is designed. Ok