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.
Printable Handouts
Navigable Slide Index
- Introduction
- Talk outline
- The brain
- The synapse
- More about the synapse
- Excitatory and inhibitory synapses
- Postsynaptic scaffold proteins: gephyrin
- Postsynaptic scaffold proteins: collybistin
- Postsynaptic scaffold proteins: dystrophin
- Postsynaptic scaffold proteins at CNS
- Complexity at inhibitory and excitatory synapses
- Synaptic strength
- AMPA receptor trafficking
- AMPAR trafficking in synaptic plasticity
- Dendritic spines
- Spine shape influences diffusion
- Dendritic spines (2)
- Spines shrink and grow during plasticity
- PSD95, SHANK and GRIP
- GRIP (Glutamate Receptor Interacting Protein)
- GRIP family protein interactions
- Role of GRIP and interactors in AMPAR trafficking
- PSD-95
- PSD-95 - the “slot” hypothesis
- PSD-95 - lateral mobility
- Regulation of synaptic plasticity
- Internalization of AMPAR
- PSD-95 as a signaling scaffold
- PSD-95 as a signaling scaffold - Kalirin
- PSD-95 as a signaling scaffold - SynGAP & SPAR
- PSD-95 as a signaling scaffold - nNOS
- PSD-95 as a signaling scaffold - AKAP
- Shank proteins
- Shank protein-interaction sites
- Scaffolding proteins in neurological disease
- Alzheimer’s disease
- Autism spectrum disorders
- Schizophrenia
- Brain ischaemia (e.g. stroke)
- PSD-95 conclusions
- GRIP
- Summary
- Acknowledgements
Topics Covered
- Multi-domain structure of scaffold proteins allows multiple protein-protein interactions
- They localise important signaling proteins close to neurotransmitter receptor complexes
- Scaffold proteins at excitatory synapses underpin synaptic plasticity by regulating AMPA receptor trafficking and dendritic spine morphology
- Mutations in scaffold proteins underlie neuropsychiatric diseases such as autism and schizophrenia
- Other diseases including Alzheimer’s and stroke also involve mechanisms incorporating postsynaptic scaffold proteins
Links
Series:
Categories:
Therapeutic Areas:
Talk Citation
Hanley, J. (2014, April 2). Postsynaptic scaffold proteins in health and disease [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 3, 2024, from https://doi.org/10.69645/RZMZ2297.Export Citation (RIS)
Publication History
Financial Disclosures
- Dr. Jonathan Hanley has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
A selection of talks on Biochemistry
Transcript
Please wait while the transcript is being prepared...
0:00
Hello, my name is Jonathan Hanley.
I'm a senior lecturer in the
Department of Biochemistry
at the University of Bristol, and
my research focuses on neuronal cell
biology, in particular molecular
mechanisms that underlie changes
in synaptic strength, otherwise
known as synaptic plasticity,
which are thought to
underlie learning and memory
and are also proposed to
be involved in a number
of neurological diseases.
In this presentation, I will try
to give an overview of a number
of proteins whose major role
is to organize synapses,
or the so-called scaffold proteins.
As the name suggests,
a scaffold protein
provide structure to the
synapse and also acts
as a platform to bring numerous
specific protein components close
together to enhance signaling,
trafficking, or other cell
biological events that are crucial
for the function of the synapse.
0:49
I will start off by introducing
some basic concepts about synapses,
their plasticity, their
molecular organization.
Since the title of this presentation
covers a very broad topic,
I will not be able to discuss
all aspects in great detail,
so I will focus on
excitatory synapses,
and beyond that I will
focus mainly on three
multi-domain scaffold proteins
called GRIP, PSD-95, and SHANK.
I will describe their
normal synaptic function,
and finally, discuss their role
in some important neurological
diseases, Alzheimer's,
autism spectrum
disorders, or ASD, schizophrenia.
and brain ischemia.
1:28
The brain is the center
of the nervous system
and almost certainly the most
complex structure in biology.
All aspects of cognition
originate in the brain.
Thoughts, emotions,
memories, ideas, and dreams.
The brain also provides
us with the ability
to see, hear, taste,
smell, touch, and move.
It allows us to form words,
understand mathematics, communicate
with others, make decisions,
compose, and appreciate art.