Neural Regeneration Research · 2016 · 18 citations · 27 references
Life SciencesNeurosciencePharmacologyMolecular NeuroscienceMolecular PharmacologyNeurochemistryBlood-brain Barrier DysfunctionBlood-brain Barrier PharmacologyCalcium SignalingHypoxic-ischemic Brain InjuryIntracellular Calcium SignalingNeuroprotectionBlood-brain Barrier PermeabilityCalpain ActivityCalpain-mediated ProteolysisCysteine Protease MechanismCysteine ProteasesHypoxic Cellular InjuryHypoxic Neuronal InjuryStructure-activity Relationship Modeling
The neuroprotective property of quercetin is well reported against hypoxia and ischemia in past studies. This property of quercetin lies in its antioxidant property with blood-brain barrier permeability and anti-inflammatory capabilities. µ-Calpain, a calcium ion activated intracellular cysteine protease causes serious cellular insult, leading to cell death in various pathological conditions including hypoxia and ischemic stroke. Hence, it may be considered as a potential drug target for the treatment of hypoxia induced neuronal injury. As the inhibitory property of µ-calpain is yet to be explored in details, hence, in the present study, we investigated the interaction of quercetin with µ-calpain through a molecular dynamics simulation study as a tool through clarifying the molecular mechanism of such inhibition and determining the probable sites and modes of quercetin interaction with the µ-calpain catalytic domain. In addition, we also investigated the structure-activity relationship of quercetin with μ-calpain. Affinity binding of quercetin with µ-calpain had a value of -28.73 kJ/mol and a Ki value of 35.87 µM that may be a probable reason to lead to altered functioning of µ-calpain. Hence, quercetin was found to be an inhibitor of µ-calpain which might have a possible therapeutic role in hypoxic injury.
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Cross-Talk between Two Cysteine Protease Families
Toshiyuki Nakagawa, Junying Yuan · The Journal of Cell Biology · 2000 · 1.2K citations · Full text