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              Printable Handouts
Navigable Slide Index
- Introduction
 - The IP3 receptor
 - Types of the IP3-R throughout the evolution
 - mRNA isomers through the development
 - Expansion of a gene: importance of function
 - IP3-R isoforms potentially exist
 - The expression of the IP3-R throughtout the cell
 - Different IP3-R paralogs have different distributions
 - Organelles in the cell
 - IP3-R identified in the ER
 - The IP3-R model
 - Ankrin regulates channel activity and stability
 - Chromagranins (Cg): Ca binding proteins
 - The physiological link between the IP3-R and Cg
 - Cg has an inhibitory effect on IP3-R function
 - ERP44:IP3-R interaction
 - Conditions in which ERP44 regulates IP3-R
 - Proteins interaction with IP3-R lumenar regions
 - CAM binding peptides
 - CaBPs (calbindin): neuronal EF hand
 - CaBPs interact with IP3-R
 - RACK1 and the heterotrimeric G protein
 - IP3-R:RACK1 interaction
 - Human B-cells C825T mutation for G-beta-3
 - IRBIT binds IP3-R near the IP3-R binding pocket
 - IRBIT is sensitive to the IP3-R binding IP3
 - Proteins interact with IP3-R: myosin, IRAG, CARP
 - Myosin: IP3R modulate pharyngeal pumping
 - CARP: carbonic anhydrase-related protein
 - CARP binding sites in the IP3-R
 - IRAG: IP3-R associated cyclic GMP kinase
 - CGK1-beta
 - The C-terminus of IP3-R
 - Ca induced apoptosis and huntigton
 - PP1A regulates IP3-R phosphorylation by PKA
 - Mechanism for alterations: IP3-R phosphorylation
 - IP3-R as a cytoskeletal element
 - The 4.1N is critical for the basal-lateral targeting
 - A multitude functional proteins interact with IP3-R
 - IP3R in the Golgi apparatus
 - Cg, Cam and CaBPs interact with IP3-R
 - Sec 6/8 are active upstream of IP3 binding site
 - IP3-R and plasma membrane interaction
 - TRPC channels: Homer, Bank and Junctate
 - The model for IP3R-TRPC interactions
 - An Inhibitory effect of TRPC on IP3-R
 - Are TRPC channels coupled to the IP3-R?
 - The role of IP3-R in the TRPC activation
 - Junctate protein interacts with IP3-R
 - Junctate stimulates Ca release
 - Proteins involved in the IP3R-TRPC complex
 - BANK protein activity
 - Proper Ca signaling
 - IP3R affects the mitochondrial Ca homeostasis
 - Apoptotic and nonapoptotic proteins
 - IP3R is juxtaposed to mitochondria
 - Ca overload is the key to cytochrome C release
 - Caspase 3 and calpein in apoptosis
 - Bcl and Bcl-xl: anti-apoptotic proteins
 - Proteins interact with IP3-R during apoptosis
 - The nucleus
 - Nuclear Ca signals are induced by hepatocytic GF
 - Why is IP3R located in the nucleus?
 - IP3R in calciosomes
 - Calciosomes
 - Why are there 23,001 isomers of IP3R?
 - IP3R isomers are necessary for function specificity
 - Conclusions
 
Topics Covered
- Activation of the IP3-receptor (IP3R), a major endoplasmic Calcium release channel in many cells, is activated by the second messenger inositol 1,4,5-trisphosphate (IP3)
 - The IP3R is unique in that it can integrate signals from numerous cellular pathways via a myriad of inputs which include nucleotide binding, phosphorylation, Calcium binding and protein-protein interactions
 - A diverse range of cellular functions are modulated by the IP3R including contraction/excitation, secretion, gene expression, cell cycle, apoptosis and cellular growth
 - The nodal properties of the IP3R and the mechanisms by which this occurs
 
Talk Citation
Patterson, R. (2007, October 1). The molecular biology of the inositol trisphosphate receptor [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved November 4, 2025, from https://doi.org/10.69645/DOFE8213.Export Citation (RIS)
Publication History
Financial Disclosures
- Dr. Randen Patterson has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.