We noted you are experiencing viewing problems
-
Check with your IT department that JWPlatform, JWPlayer and Amazon AWS & CloudFront are not being blocked by your network. The relevant domains are *.jwplatform.com, *.jwpsrv.com, *.jwpcdn.com, jwpltx.com, jwpsrv.a.ssl.fastly.net, *.amazonaws.com and *.cloudfront.net. The relevant ports are 80 and 443.
-
Check the following talk links to see which ones work correctly:
Auto Mode
HTTP Progressive Download Send us your results from the above test links at access@hstalks.com and we will contact you with further advice on troubleshooting your viewing problems. -
No luck yet? More tips for troubleshooting viewing issues
-
Contact HST Support access@hstalks.com
-
Please review our troubleshooting guide for tips and advice on resolving your viewing problems.
-
For additional help, please don't hesitate to contact HST support access@hstalks.com
We hope you have enjoyed this limited-length demo
This is a limited length demo talk; you may
login or
review methods of
obtaining more access.
Topics Covered
- Muscarinic acetylcholine receptors
- Neurological drug discovery
- Schizophrenia and Alzheimer’s disease
- Structure-based drug design
- Allosteric GPCR modulation
Biography
Prof. Andrew B. Tobin is Professor of Molecular Pharmacology at the Centre for Translational Pharmacology, School of Molecular Biosciences, University of Glasgow, UK, where he also serves as Director of the Advanced Research Centre. His research focuses on understanding how G protein-coupled receptors (GPCRs) function and how mechanisms such as receptor phosphorylation influence signalling and drug action.
He and his group apply genetic, proteomic and pharmacological approaches to probe GPCR biology and to inform the rational design of next-generation therapeutics. His work spans basic pharmacology, mouse models of disease and translational studies, including efforts targeting neurodegeneration and infectious diseases such as malaria.
Links
Series:
Categories:
Therapeutic Areas:
Talk Citation
Tobin, A.B. (2026, March 31). Muscarinic acetylcholine receptor modulation in neurological diseases [Audio file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved April 18, 2026, from https://doi.org/10.69645/ZJTL4168.Export Citation (RIS)
Publication History
- Published on March 31, 2026
Financial Disclosures
- Prof. Andrew B. Tobin has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
Other Talks in the Playlist: Research Interviews
Transcript
Please wait while the transcript is being prepared...
0:00
Interviewer: Muscarinic
acetylcholine receptors have
long been proposed as
promising targets for treating
neurological disorders such as
schizophrenia and
Alzheimer's disease.
But only recently, the
first drug targeting
these receptors has
received clinical approval.
In this interview, we are
joined by Prof. Andrew Tobin,
Director of the Advanced
Research Centre at
the University of Glasgow to
discuss ongoing challenges,
recent breakthroughs and the
potential for developing
additional novel therapies based
on our knowledge of
these receptors.
Prof. Tobin, thank you very
much for joining us today.
To kick things off, can you
please tell us a little bit
about why muscarinic
acetylcholine receptors,
particularly the M1
and the M4 subtypes
have been considered
promising targets for
neurological disorders
and what have been
the main barriers
to developing drugs
targeting them over
the past decades?
Prof. Tobin: Thank you
very much for the invitation
to speak to you today, and
this opportunity to talk about
my favorite subject which
is muscarinic receptors.
There has been a great deal of
interest in these receptors
for some decades now, and the
primary reason for that is
very early pharmacological
data and indeed genetic data
in mouse knockout studies
that have indicated that
certainly the M1
muscarinic receptor,
and indeed, the M4
muscarinic receptor,
as you all know, there
are five subtypes
of this G protein-coupled
receptor family,
M1 and M4 being
the primary targets of
interest for the treatment of
symptomatic memory loss
in Alzheimer's disease,
and subsequently, for
the correction of