Academic Journal

Docking Simulation of the Binding Interactions of Saxitoxin Analogs Produced by the Marine Dinoflagellate Gymnodinium catenatum to the Voltage-Gated Sodium Channel Nav1.4

التفاصيل البيبلوغرافية
العنوان: Docking Simulation of the Binding Interactions of Saxitoxin Analogs Produced by the Marine Dinoflagellate Gymnodinium catenatum to the Voltage-Gated Sodium Channel Nav1.4
المؤلفون: Lorena M. Durán-Riveroll, Allan D. Cembella, Christine J. Band-Schmidt, José J. Bustillos-Guzmán, José Correa-Basurto
المصدر: Toxins, Vol 8, Iss 5, p 129 (2016)
بيانات النشر: MDPI AG, 2016.
سنة النشر: 2016
المجموعة: LCC:Medicine
مصطلحات موضوعية: voltage-gated sodium channel, benzoyl saxitoxin analogs, molecular docking, binding affinity, Medicine
الوصف: Saxitoxin (STX) and its analogs are paralytic alkaloid neurotoxins that block the voltage-gated sodium channel pore (Nav), impeding passage of Na+ ions into the intracellular space, and thereby preventing the action potential in the peripheral nervous system and skeletal muscle. The marine dinoflagellate Gymnodinium catenatum produces an array of such toxins, including the recently discovered benzoyl analogs, for which the mammalian toxicities are essentially unknown. We subjected STX and its analogs to a theoretical docking simulation based upon two alternative tri-dimensional models of the Nav1.4 to find a relationship between the binding properties and the known mammalian toxicity of selected STX analogs. We inferred hypothetical toxicities for the benzoyl analogs from the modeled values. We demonstrate that these toxins exhibit different binding modes with similar free binding energies and that these alternative binding modes are equally probable. We propose that the principal binding that governs ligand recognition is mediated by electrostatic interactions. Our simulation constitutes the first in silico modeling study on benzoyl-type paralytic toxins and provides an approach towards a better understanding of the mode of action of STX and its analogs.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2072-6651
Relation: http://www.mdpi.com/2072-6651/8/5/129; https://doaj.org/toc/2072-6651
DOI: 10.3390/toxins8050129
URL الوصول: https://doaj.org/article/a9900e0fbff34a3ab5061165ecab4458
رقم الانضمام: edsdoj.9900e0fbff34a3ab5061165ecab4458
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20726651
DOI:10.3390/toxins8050129