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Printable Handouts
Navigable Slide Index
- Introduction
- Lipids regulate cellular communication
- The phosphoinositide polyphosphates
- Signaling as viewed from Salt Lake City
- PI localization in membrane trafficking pathways
- Synthetic phosphoinositide probes
- Intracellular delivery of phosphoinositides (1)
- Intracellular delivery of phosphoinositides (2)
- Intracellular delivery of PI into NIH 3T3 fibroblasts
- Reconstruction of PI(3,4)P2-NBD and histone-TMR
- Ins(1,4,5)P3 and PtdIns(4,5)P2 stimulate Ca fluxes
- Calcium oscillations initiated by shuttled PI(4,5)P3
- Exogenous phosphoinositides elicit cell responses
- Neutrophils polarize and follow chemoattractants
- PtdIns(3,4,5)P3 induces polarization and migration
- PI 3-K and RhoGTPase required for polarization
- PI(4)P rescues recruitment of AP-1 to golgi
- PI(3,4,5)P3 causes GLUT4 incorporation
- Metabolically-stabilized phosphoinositides
- Phosphoinositides are remodeled by enzymes
- Phospholipase C-resistant PI(4,5)P2 analogs
- Synthesis of stabilized PtdIns(4,5)P2 analogs
- PLC-resistant PtdIns(4,5)P2 analogs
- PLC-resistant PtdIns(4,5)P2 - no Ca2+ release
- Phosphatase-resistant PtdIns(3)P analogs
- PI(3)P analogs bind to FYVE and PX domains
- Are ms-PI(3)Ps substrates for PIKfyve?
- Ms-PI(3)Ps are phosphorylated by PIKfyve
- Phosphatase-resistant PtdIns(3,4,5)P3 analogs
- New chemistries for PIP tethering
- Synthetic two-headed lipids: PE and PIP heads
- SPR: Grp1 binds biotinylated Hy-PIP4
- Hy-PIPn-TMR self-shuttles to plasma membrane
- Head group spin-labeled Hy-PI(3)P
- Fluorescent Hy-PIPsTM in plasma membrane
- Hy-PIPsTM: better than acyl-modified PIPs
- PolyPIPosomesTM: polymerized PIPn-liposomes
- Comparing binding kinetics by SPR
- Tethers compared: global SPR analysis
- Relative affinities from SPR
- The PHD finger of RAG2 modulates V(D)J
- PolyPIPosomesTM: advantages
- Fishing with tethered IPs and PIPs
- Functional lipidomics: the next frontier
- Different baits catch different fish
- ING2 first isolated as a PI(3,4,5)P3 binding protein
- ING2 PHD binds PI(5)P selectively
- Nuclear ING2 lipid-Zn finger complex
- Co-localization of ING2 PHD and TR-PI(5)P
- Mining for signaling by functional proteomics
- Mass spec identifies protein complexes
- Functional proteolipidome
- Anti-PIP antibodies
- Anti-PI(3,4,5)P3 immunogen: a tool to detect PIP4
- PIP3 and PIP2 in PDGF-stimulated 3T3 fibroblasts
- PI(4,5)P2 co-localizes with nuclear markers
- Insulin and leptin activate PI3-K
- Anti-PI(4,5)P2 co-localizes with PLCd PH domain
- Defective signaling leads to excess PIP4
- Lipid signaling oncogenes in ovarian cancer
- Immunodetection of PI(3,4,5)P3 in tissues
- Visualizing PLA2 and PLD activity
- Fluorogenic substrates to measure PLA activity
- DBPC and BBPC fluorogenic cleavage by sPLA3
- cPLA2 activity in living MDCK-D1 cells
- Detection of iPLA2 activity in cancer cells
- Oxo-M stimulates fatty acid release via cPLA3
- Enzyme-assisted fluorogenic substrates synthesis
- Head group selectivity of PLA hydrolysis
- Fluorogenic assay for PLD activity
- Enzyme-assisted synthesis of PLD substrates
- Dimethyl analog with Strep. chromofuscus PLD
- Summary
- Acknowledgements (1)
- Acknowledgements (2)
- Utah (1)
- Utah (2)
Topics Covered
- Making and using phosphoinositide phosphate (PIP) affinity probes
- Effects of exogenous PIPs
- Metabolically-stabilized PIPs
- New tethering strategies
- Signaling proteomics
- Antibodies to PIPs
- Visualizing phospholipase A and D activity with fluorogenic probes
Talk Citation
Prestwich, G. (2022, April 12). Visualizing and manipulating phosphoinositide and phospholipid signaling [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 22, 2024, from https://doi.org/10.69645/KSIA4542.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Glenn Prestwich has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
Visualizing and manipulating phosphoinositide and phospholipid signaling
A selection of talks on Biochemistry
Transcript
Please wait while the transcript is being prepared...
0:00
Hello, this is Glenn Prestwich,
I'm a professor of medicinal chemistry
at the University of Utah, and
I'm going to be talking today about the
use of chemical probes for visualizing and
manipulating phosphoinositide and
phospholipid signaling in cells.
0:14
Lipids are important mediators
of cellular communication,
they can occur both outside the cells in
the extracellular medium, or inside cells.
The external messengers, such as
lysophosphatidic acid are important cell
mitogens and control cell migration and
proliferation,
whereas messengers that are inside the
cells, such as the phosphoinositides and
other phospholipids on the inner leaflet,
recruit proteins and
the complexes then end up controlling
cell shape, cytoskeletal rearrangements,
cell survival, cell differentiation and
metabolic events within the cell.
0:47
The poly-phosphoinositides
occur in eight chemical forms.
There is the phosphatidylinositol itself,
with no additional phosphates on
the myo-inositol head group attached
through a phosphodiester bond to
a diacylglycerol moiety, or
you can have a single phosphate,
as in the phosphomonoesters PI(3)P,
PI(4)P and PI(5)P.
You can have three different forms of
phosphoinositide bisphosphates such as
PI(4,5)P2, PI(3,4)P2 and PI(3,5)P2, or
a single trisphosphate PI(3,4,5)P3.
For additional information on the
synthesis of the native phosphoinositides
and their affinity probes, and for
the uses of these, I would refer
the listener to review articles as
shown in the bottom of the slide.
1:34
In Salt Lake City we view phosphoinositide
signaling in a slightly different way,
we view it in three dimensions, where the
phosphoinositide energy requiring kinase
is using ATP to put additional phosphates
onto the phosphoinositide head-group and
ultimately getting to
Mount Supreme up there.
PIP3 is the most highly phosphorylated and
most highly interactive phosphoinositide,
giving rise to mitogenic effects
in cell growth, carcinogenesis,
abnormal as well as normal responses in
inflammatory and immune response, and
in normally controlling
the insulin response.
In addition to the kinases
there are phosphatases which
remove phosphate groups,
as well as phospholipases.
We'll talk more about these and how to
manipulate those later on in this talk.
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