The Sea Anemone Neurotoxins Modulating Sodium Channels: An Insight at Structure and Functional Activity after Four Decades of Investigation

Many human cardiovascular and neurological disorders (such as ischemia, epileptic seizures, traumatic brain injury, neuropathic pain, etc.) are associated with the abnormal functional activity of voltage-gated sodium channels (VGSCs/Na<sub>V</sub>s). Many natural toxins, including the se...

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Main Authors: Margarita Mikhailovna Monastyrnaya, Rimma Sergeevna Kalina, Emma Pavlovna Kozlovskaya
Format: Article
Language:English
Published: MDPI AG 2022-12-01
Series:Toxins
Subjects:
Online Access:https://www.mdpi.com/2072-6651/15/1/8
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author Margarita Mikhailovna Monastyrnaya
Rimma Sergeevna Kalina
Emma Pavlovna Kozlovskaya
author_facet Margarita Mikhailovna Monastyrnaya
Rimma Sergeevna Kalina
Emma Pavlovna Kozlovskaya
author_sort Margarita Mikhailovna Monastyrnaya
collection DOAJ
description Many human cardiovascular and neurological disorders (such as ischemia, epileptic seizures, traumatic brain injury, neuropathic pain, etc.) are associated with the abnormal functional activity of voltage-gated sodium channels (VGSCs/Na<sub>V</sub>s). Many natural toxins, including the sea anemone toxins (called neurotoxins), are an indispensable and promising tool in pharmacological researches. They have widely been carried out over the past three decades, in particular, in establishing different Na<sub>V</sub> subtypes functional properties and a specific role in various pathologies. Therefore, a large number of publications are currently dedicated to the search and study of the structure-functional relationships of new sea anemone natural neurotoxins–potential pharmacologically active compounds that specifically interact with various subtypes of voltage gated sodium channels as drug discovery targets. This review presents and summarizes some updated data on the structure-functional relationships of known sea anemone neurotoxins belonging to four structural types. The review also emphasizes the study of type 2 neurotoxins, produced by the tropical sea anemone <i>Heteractis crispa</i>, five structurally homologous and one unique double-stranded peptide that, due to the absence of a functionally significant Arg14 residue, loses toxicity but retains the ability to modulate several VGSCs subtypes.
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spelling doaj.art-d21ca994c3bd431bae08ad52371c2c7d2023-12-01T00:56:22ZengMDPI AGToxins2072-66512022-12-01151810.3390/toxins15010008The Sea Anemone Neurotoxins Modulating Sodium Channels: An Insight at Structure and Functional Activity after Four Decades of InvestigationMargarita Mikhailovna Monastyrnaya0Rimma Sergeevna Kalina1Emma Pavlovna Kozlovskaya2G.B. Elyakov Pacific Institute of Bioorganic Chemistry, Far Eastern Branch of the Russian Academy of Science, 690022 Vladivostok, RussiaG.B. Elyakov Pacific Institute of Bioorganic Chemistry, Far Eastern Branch of the Russian Academy of Science, 690022 Vladivostok, RussiaG.B. Elyakov Pacific Institute of Bioorganic Chemistry, Far Eastern Branch of the Russian Academy of Science, 690022 Vladivostok, RussiaMany human cardiovascular and neurological disorders (such as ischemia, epileptic seizures, traumatic brain injury, neuropathic pain, etc.) are associated with the abnormal functional activity of voltage-gated sodium channels (VGSCs/Na<sub>V</sub>s). Many natural toxins, including the sea anemone toxins (called neurotoxins), are an indispensable and promising tool in pharmacological researches. They have widely been carried out over the past three decades, in particular, in establishing different Na<sub>V</sub> subtypes functional properties and a specific role in various pathologies. Therefore, a large number of publications are currently dedicated to the search and study of the structure-functional relationships of new sea anemone natural neurotoxins–potential pharmacologically active compounds that specifically interact with various subtypes of voltage gated sodium channels as drug discovery targets. This review presents and summarizes some updated data on the structure-functional relationships of known sea anemone neurotoxins belonging to four structural types. The review also emphasizes the study of type 2 neurotoxins, produced by the tropical sea anemone <i>Heteractis crispa</i>, five structurally homologous and one unique double-stranded peptide that, due to the absence of a functionally significant Arg14 residue, loses toxicity but retains the ability to modulate several VGSCs subtypes.https://www.mdpi.com/2072-6651/15/1/8sea anemoneneurotoxins of types 1–4voltage-gated sodium channelselectrophysiologymolecular modeling
spellingShingle Margarita Mikhailovna Monastyrnaya
Rimma Sergeevna Kalina
Emma Pavlovna Kozlovskaya
The Sea Anemone Neurotoxins Modulating Sodium Channels: An Insight at Structure and Functional Activity after Four Decades of Investigation
Toxins
sea anemone
neurotoxins of types 1–4
voltage-gated sodium channels
electrophysiology
molecular modeling
title The Sea Anemone Neurotoxins Modulating Sodium Channels: An Insight at Structure and Functional Activity after Four Decades of Investigation
title_full The Sea Anemone Neurotoxins Modulating Sodium Channels: An Insight at Structure and Functional Activity after Four Decades of Investigation
title_fullStr The Sea Anemone Neurotoxins Modulating Sodium Channels: An Insight at Structure and Functional Activity after Four Decades of Investigation
title_full_unstemmed The Sea Anemone Neurotoxins Modulating Sodium Channels: An Insight at Structure and Functional Activity after Four Decades of Investigation
title_short The Sea Anemone Neurotoxins Modulating Sodium Channels: An Insight at Structure and Functional Activity after Four Decades of Investigation
title_sort sea anemone neurotoxins modulating sodium channels an insight at structure and functional activity after four decades of investigation
topic sea anemone
neurotoxins of types 1–4
voltage-gated sodium channels
electrophysiology
molecular modeling
url https://www.mdpi.com/2072-6651/15/1/8
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