Inositol trisphosphate receptor

Inositol trisphosphate receptor (InsP3R) is a membrane glycoprotein complex acting as a Ca²⁺ channel activated by inositol trisphosphate (InsP3). InsP3R is very diverse among organisms, and is necessary for the control of cellular and physiological processes including cell division, cell proliferation, apoptosis, fertilization, development, behavior, learning and memory.<ref name="pmid12442173">Template:Cite journal</ref> Inositol triphosphate receptor represents a dominant second messenger leading to the release of Ca²⁺ from intracellular store sites. There is strong evidence suggesting that the InsP3R plays an important role in the conversion of external stimuli to intracellular Ca²⁺ signals characterized by complex patterns relative to both space and time, such as Ca²⁺ waves and oscillations.<ref name="pmid9243320">Template:Cite journal</ref>

Discovery

The InsP3 receptor was first purified from rat cerebellum by neuroscientists Surachai Supattapone and Solomon Snyder at Johns Hopkins University School of Medicine.<ref name="pmid2826483">Template:Cite journal</ref>

The cDNA of the InsP3 receptor was first cloned in the laboratory of Katsuhiko Mikoshiba. The initial sequencing was reported as an unknown protein enriched in the cerebellum called P400.<ref name="pmid2762133">Template:Cite journal</ref> The large size of this open reading frame indicated a molecular weight similar to the protein purified biochemically, and soon thereafter it was confirmed that the protein p400 was in fact the inositol trisphosphate receptor.<ref name="pmid2554142">Template:Cite journal</ref>

Distribution

The receptor has a broad tissue distribution but is especially abundant in the cerebellum. Most of the InsP3Rs are found integrated into the endoplasmic reticulum.

Structure

Several X-ray crystallographic <ref>Template:Cite journal</ref><ref>Template:Cite journal</ref><ref>Template:Cite journal</ref> and electron cryomicroscopic (cryo-EM) <ref>Template:Cite journal</ref><ref>Template:Cite journal</ref><ref>Template:Cite journal</ref><ref>Template:Cite journal</ref><ref>Template:Cite journal</ref><ref>Template:Cite journal</ref><ref>Template:Cite journal</ref> structures of IP₃Rs from mouse, rat, and human have defined the overall architecture of the channel. The 1.2 MDa C4-symmetric assembly consists of an ER-embedded transmembrane domain (TMD) in a domain-swapped 6 transmembrane (6TM) cation channel fold that is capped by a large cytosolic domain (CD). In this manner, IP₃Rs share significant homology with the much larger and distantly-related RyRs.<ref>Template:Cite journal</ref> The CD contains all known ligand binding sites, including the IP₃ binding site, two Ca²⁺ binding sites, an adenine nucleotide binding site, and a C₂H₂ Zn²⁺ finger fold. A comprehensive Ca²⁺-dependent conformational landscape has been defined by cryo-EM.<ref>Template:Cite journal</ref>

See also

• Inositol
• Inositol phosphate
  • Inositol monophosphate
  • Inositol trisphosphate
  • Inositol pentakisphosphate
  • Inositol hexaphosphate
• MRVI1 associated through complex formation.

External links

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