1. Metabolic Enzyme/Protease
  2. Phospholipase
  3. Phosphatidylinositol 4,5-bisphosphate

Phosphatidylinositol 4,5-bisphosphate  (Synonyms: L-alpha-Phosphatidylinositol-4,5-bisphosphate; (PtdIns)-(4,5)-P2)

Cat. No.: HY-114457
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Phosphatidylinositol 4,5-bisphosphate (L-alpha-Phosphatidylinositol-4,5-bisphosphate) is a plasma membrane lipid that is enriched in the cytoplasmic leaflet of the plasma membrane. Phosphatidylinositol 4,5-bisphosphate serves as a substrate for phospholipase C and class I PI3K, generating diacylglycerol, inositol (1,4,5)-trisphosphate, and phosphatidylinositol (3,4,5)-trisphosphate. Phosphatidylinositol 4,5-bisphosphate contributes to lamellipodial protrusion, directional cell migration, focal adhesion lipid generation, and trafficking of the GABAA receptor. Phosphatidylinositol 4,5-bisphosphate can be used in research related to acute lung injury and pulmonary edema.

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Phosphatidylinositol 4,5-bisphosphate

Phosphatidylinositol 4,5-bisphosphate Chemical Structure

CAS No. : 245126-95-8

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Description

Phosphatidylinositol 4,5-bisphosphate (L-alpha-Phosphatidylinositol-4,5-bisphosphate) is a plasma membrane lipid that is enriched in the cytoplasmic leaflet of the plasma membrane. Phosphatidylinositol 4,5-bisphosphate serves as a substrate for phospholipase C and class I PI3K, generating diacylglycerol, inositol (1,4,5)-trisphosphate, and phosphatidylinositol (3,4,5)-trisphosphate. Phosphatidylinositol 4,5-bisphosphate contributes to lamellipodial protrusion, directional cell migration, focal adhesion lipid generation, and trafficking of the GABAA receptor. Phosphatidylinositol 4,5-bisphosphate can be used in research related to acute lung injury and pulmonary edema[1][2][3].

In Vitro

Phosphatidylinositol 4,5-bisphosphate (L-alpha-Phosphatidylinositol-4,5-bisphosphate) (10-25 μM, endogenous levels; 200-400 s, 250 s) and its water-soluble analog diC8-PI(4,5)P2 maintain the conductive state of wild-type mouse ANO1 channels in HEK cells by preventing Ca2+-induced inactivation and rescuing channel activity after PI(4,5)P2 depletion[2].
Phosphatidylinositol 4,5-bisphosphate (PI(4,5)P2) (10 μM) binds to specific residues in multiple sites on mouse ANO1 channels to regulate channel gating and prevent Ca2+-induced inactivation, with mutations in these sites eliminating or reducing PI(4,5)P2 sensitivity[2].
Phosphatidylinositol 4,5-bisphosphate (PI(4,5)P2) modulates the conformation of mouse ANO1 channels by inducing TM6 rotation, which prevents Ca2+-induced pore collapse and maintains the conductive channel state[2].
Phosphatidylinositol 4,5-bisphosphate constitutes 1-2 mol% of total mammalian plasma membrane lipid, with a specific stearic acid-arachidonic acid acyl chain profile, and is the most abundant cellular phosphoinositide[3].
Phosphatidylinositol 4,5-bisphosphate acts as a substrate for mammalian PLC isoforms, whose hydrolysis produces the second messengers IP3 and DAG to drive downstream Ca2+ and PKC signaling[3].
Phosphatidylinositol 4,5-bisphosphate dynamically regulates mammalian actin cytoskeleton dynamics by modulating the activity and localization of actin-binding proteins, including ERM proteins, cofilin, and N-WASP, with PLC-mediated PI(4,5)P2 depletion driving actin disassembly and cell migration in carcinoma cells[3].
Phosphatidylinositol 4,5-bisphosphate is essential for multiple steps of mammalian clathrin-mediated endocytosis, including AP2 activation, clathrin recruitment, membrane deformation, dynamin-mediated scission, and regulation of vesicle uncoating via localized production and degradation[3].
Phosphatidylinositol 4,5-bisphosphate directly regulates the activity and localization of multiple mammalian plasma membrane ion channels, maintaining Kir and KCNQ channels in an open state, inhibiting TRPV4 channels, and contributing to GABAA receptor membrane localization, with PLC-mediated PI(4,5)P2 depletion dynamically altering channel activity[3].
Phosphatidylinositol 4,5-bisphosphate forms nanoscale clusters (~65-73 nm) in the mammalian plasma membrane, with a portion bound to cytoskeletal proteins, and its local enrichment is regulated by lipid raft trapping, protein sequestration, and localized synthesis[3].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Phosphatidylinositol 4,5-bisphosphate (L-alpha-Phosphatidylinositol-4,5-bisphosphate) (150-750 μM; intrapulmonary instillation; single dose) dose-dependently stimulates alveolar fluid clearance in normal male and female Sprague Dawley rats via an amiloride/ENaC-dependent pathway, with an EC50 of 170 μM in males and ~93% increased clearance at 300 μM in both genders, and membrane residency is required for full stimulatory activity[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Sprague Dawley (male, 300-350 g; female, 275-325 g; ovariectomized female)[1]
Dosage: 150 μM; 300 μM; 750 μM
Administration: intrapulmonary instillation; single dose
Result: Dose-dependently increased alveolar fluid clearance relative to 0 μM control in male rats.
Reached an EC50 of 170 μM for stimulation of alveolar fluid clearance in male rats.
Did not produce additional alveolar fluid clearance stimulation beyond terbutaline alone when co-instilled with 10-4 M terbutaline at 300 μM dose.
Was not inhibited when co-instilled with 10-4 M propranolol at 300 μM dose.
Showed that its membrane-binding-deficient analog (300 μM phosphatidylinositol 4,5-bisphosphate amine) stimulated alveolar fluid clearance to an intermediate level between 300 μM phosphatidylinositol 4,5-bisphosphate and control, with absolute values of 6.8 in males and 6.2 in females.
Masse moléculaire

1047.09

Formule

C47H85O19P3

CAS No.
SMILES

O=P(O)(O)O[C@H]1[C@@H]([C@H]([C@@H](O)[C@@H](OP(OC[C@@H](COC(CCCCCCCCCCCCCCCCC)=O)OC(CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC)=O)(O)=O)[C@@H]1O)O)OP(O)(O)=O

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Nom du produit:
Phosphatidylinositol 4,5-bisphosphate
Cat. No.:
HY-114457
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