Toxicon : official journal of the International Society on Toxinology · 2013
Venom toxins in the exploration of molecular, physiological and pathophysiological functions of acid-sensing ion channels.
СтатьяПоддержка исследования: вне правительства СШАОбзорНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Baron Anne, Diochot Sylvie, Salinas Miguel, Deval Emmanuel, Noël Jacques, Lingueglia Eric
Аннотация
Acid-sensing ion channels (ASICs) are voltage-independent proton-gated cation channels that are largely expressed in the nervous system as well as in some non-neuronal tissues. In rodents, six different isoforms (ASIC1a, 1b, 2a, 2b, 3 and 4) can associate into homo- or hetero-trimers to form a functional channel. Specific polypeptide toxins targeting ASIC channels have been isolated from the venoms of spider (PcTx1), sea anemone (APETx2) and snakes (MitTx and mambalgins). They exhibit different and sometimes partially overlapping pharmacological profiles and are usually blockers of ASIC channels, except for MitTx, which is a potent activator. This review focuses on the use of these toxins to explore the structure-function relationships, the physiological and the pathophysiological roles of ASIC channels, illustrating at the same time the therapeutic potential of some of these natural compounds.
Предметные рубрики MeSH
Acid Sensing Ion ChannelsAmino Acid SequenceAmygdalaAnimalsAnti-Anxiety AgentsAnti-Inflammatory AgentsAntidepressive AgentsGene Expression RegulationHumansHydrogen-Ion ConcentrationMolecular Sequence DataMuscle, Smooth, VascularNeuronsNeuroprotective AgentsPeptidesProtein ConformationRodentiaSea AnemonesSnakesSpidersStructure-Activity RelationshipToxins, BiologicalVasoconstrictionVenoms