| 词条 | Phosphatidylinositol |
| 释义 |
| verifiedrevid = 409517204 | ImageFile = Phosphatidylinositol.png | ImageSize = | IUPACName = | OtherNames = PI, PtdIns |Section1={{Chembox Identifiers | CASNo_Ref = {{cascite|correct|??}} | CASNo = | PubChem = | SMILES = }} |Section2={{Chembox Properties | Formula = C47H83O13P | MolarMass = 886.56 g/mol, neutral with fatty acid composition - 18:0, 20:4 | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = }} |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} }} Phosphatidylinositol consists of a family of lipids as illustrated on the right, a class of the phosphatidylglycerides. In such molecules the isomer of the inositol group is assumed to be the myo- conformer unless otherwise stated. Typically phosphatidylinositols form a minor component on the cytosolic side of eukaryotic cell membranes. The phosphate group gives the molecules a negative charge at physiological pH. The form of phosphatidylinositol comprising the isomer muco-inositol acts as a sensory receptor in the taste function of the sensory system. In this context it is often referred to as PtdIns, but that does not imply any molecular difference from phosphatidylinositols comprising the myo- conformers of inositol. The phosphatidylinositol can be phosphorylated to form phosphatidylinositol phosphate (PI-4-P, referred to as PIP in close context or informally), phosphatidylinositol bisphosphate (PIP2) and phosphatidylinositol trisphosphate (PIP3). All lipids based on phosphatidylinositol are known as inositides, or sometimes phosphoinositides. BiosynthesisThe synthesis of phosphatidylinositol in the laboratory is catalyzed by phosphatidylinositol synthase and involves CDP-diacylglycerol and L-myo-inositol.[1] ChemistryPI has a polar and non-polar region, making the lipid an amphiphile. Phosphatidylinositol is classified as a glycerophospholipid that contains a glycerol backbone, two non-polar fatty acid tails, a phosphate group substituted with an inositol polar head group. The most common fatty acids of phosphoinositides are stearic acid in the SN1 position and arachidonic acid, in the SN2 position. Hydrolysis of phosphoinositides yield one mole of glycerol, two moles of fatty acids, one mole of inositol and one, two, or three moles of phosphoric acids, depending on the number of phosphates on the inositol rings. Phosphoinositides are regarded as the most acidic phospholipids. The specific fatty acids of PtdIns, and their conformation, employed in the sensory neurons has not been elucidated. PhosphoinositidesPhosphorylated forms of phosphatidylinositol (PI) are called phosphoinositides and play important roles in lipid signaling, cell signaling and membrane trafficking. The inositol ring can be phosphorylated by a variety of kinases on the three, four and five hydroxyl groups in seven different combinations. However, the two and six hydroxyl groups are typically not phosphorylated due to steric hindrance. All seven variations of the following phosphoinositides have been found in animals: Phosphatidylinositol monophosphates:
Phosphatidylinositol bisphosphates:
Phosphatidylinositol trisphosphate:
These phosphoinositides are also found in plant cells, with the exception of PIP3.[2] See also{{commons category|Phosphatidylinositol}}
References1. ^1 {{cite book | title=Biochemistry Third Edition| last=Mathews| first=Chrisotphe K. |author2=van Holde, K.E. |author3=Ahern, Kevin G.| year=2005}} 2. ^{{cite book | title=Inositol Phospholipid Metabolism in Arabidopsis. Characterized and Putative Isoforms of Inositol Phospholipid Kinase and Phosphoinositide-Specific Phospholipase C| last=Muller-Roeber B| first=Pical C|author2=,| year=2002}} Additional imagesExternal links
2 : Phospholipids|Membrane biology |
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