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Molecular Surface of JZTX-V (β-Theraphotoxin-Cj2a) Interacting with Voltage-Gated Sodium Channel Subtype Na(V)1.4

Voltage-gated sodium channels (VGSCs; Na(V)1.1–Na(V)1.9) have been proven to be critical in controlling the function of excitable cells, and human genetic evidence shows that aberrant function of these channels causes channelopathies, including epilepsy, arrhythmia, paralytic myotonia, and pain. The...

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Detalles Bibliográficos
Autores principales: Luo, Ji, Zhang, Yiya, Gong, Mengting, Lu, Shanshan, Ma, Yifeng, Zeng, Xiongzhi, Liang, Songping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113750/
https://www.ncbi.nlm.nih.gov/pubmed/25055801
http://dx.doi.org/10.3390/toxins6072177
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author Luo, Ji
Zhang, Yiya
Gong, Mengting
Lu, Shanshan
Ma, Yifeng
Zeng, Xiongzhi
Liang, Songping
author_facet Luo, Ji
Zhang, Yiya
Gong, Mengting
Lu, Shanshan
Ma, Yifeng
Zeng, Xiongzhi
Liang, Songping
author_sort Luo, Ji
collection PubMed
description Voltage-gated sodium channels (VGSCs; Na(V)1.1–Na(V)1.9) have been proven to be critical in controlling the function of excitable cells, and human genetic evidence shows that aberrant function of these channels causes channelopathies, including epilepsy, arrhythmia, paralytic myotonia, and pain. The effects of peptide toxins, especially those isolated from spider venom, have shed light on the structure–function relationship of these channels. However, most of these toxins have not been analyzed in detail. In particular, the bioactive faces of these toxins have not been determined. Jingzhaotoxin (JZTX)-V (also known as β-theraphotoxin-Cj2a) is a 29-amino acid peptide toxin isolated from the venom of the spider Chilobrachys jingzhao. JZTX-V adopts an inhibitory cysteine knot (ICK) motif and has an inhibitory effect on voltage-gated sodium and potassium channels. Previous experiments have shown that JZTX-V has an inhibitory effect on TTX-S and TTX-R sodium currents on rat DRG cells with IC(50) values of 27.6 and 30.2 nM, respectively, and is able to shift the activation and inactivation curves to the depolarizing and the hyperpolarizing direction, respectively. Here, we show that JZTX-V has a much stronger inhibitory effect on Na(V)1.4, the isoform of voltage-gated sodium channels predominantly expressed in skeletal muscle cells, with an IC(50) value of 5.12 nM, compared with IC(50) values of 61.7–2700 nM for other heterologously expressed Na(V)1 subtypes. Furthermore, we investigated the bioactive surface of JZTX-V by alanine-scanning the effect of toxin on Na(V)1.4 and demonstrate that the bioactive face of JZTX-V is composed of three hydrophobic (W5, M6, and W7) and two cationic (R20 and K22) residues. Our results establish that, consistent with previous assumptions, JZTX-V is a Janus-faced toxin which may be a useful tool for the further investigation of the structure and function of sodium channels.
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spelling pubmed-41137502014-07-29 Molecular Surface of JZTX-V (β-Theraphotoxin-Cj2a) Interacting with Voltage-Gated Sodium Channel Subtype Na(V)1.4 Luo, Ji Zhang, Yiya Gong, Mengting Lu, Shanshan Ma, Yifeng Zeng, Xiongzhi Liang, Songping Toxins (Basel) Article Voltage-gated sodium channels (VGSCs; Na(V)1.1–Na(V)1.9) have been proven to be critical in controlling the function of excitable cells, and human genetic evidence shows that aberrant function of these channels causes channelopathies, including epilepsy, arrhythmia, paralytic myotonia, and pain. The effects of peptide toxins, especially those isolated from spider venom, have shed light on the structure–function relationship of these channels. However, most of these toxins have not been analyzed in detail. In particular, the bioactive faces of these toxins have not been determined. Jingzhaotoxin (JZTX)-V (also known as β-theraphotoxin-Cj2a) is a 29-amino acid peptide toxin isolated from the venom of the spider Chilobrachys jingzhao. JZTX-V adopts an inhibitory cysteine knot (ICK) motif and has an inhibitory effect on voltage-gated sodium and potassium channels. Previous experiments have shown that JZTX-V has an inhibitory effect on TTX-S and TTX-R sodium currents on rat DRG cells with IC(50) values of 27.6 and 30.2 nM, respectively, and is able to shift the activation and inactivation curves to the depolarizing and the hyperpolarizing direction, respectively. Here, we show that JZTX-V has a much stronger inhibitory effect on Na(V)1.4, the isoform of voltage-gated sodium channels predominantly expressed in skeletal muscle cells, with an IC(50) value of 5.12 nM, compared with IC(50) values of 61.7–2700 nM for other heterologously expressed Na(V)1 subtypes. Furthermore, we investigated the bioactive surface of JZTX-V by alanine-scanning the effect of toxin on Na(V)1.4 and demonstrate that the bioactive face of JZTX-V is composed of three hydrophobic (W5, M6, and W7) and two cationic (R20 and K22) residues. Our results establish that, consistent with previous assumptions, JZTX-V is a Janus-faced toxin which may be a useful tool for the further investigation of the structure and function of sodium channels. MDPI 2014-07-23 /pmc/articles/PMC4113750/ /pubmed/25055801 http://dx.doi.org/10.3390/toxins6072177 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Luo, Ji
Zhang, Yiya
Gong, Mengting
Lu, Shanshan
Ma, Yifeng
Zeng, Xiongzhi
Liang, Songping
Molecular Surface of JZTX-V (β-Theraphotoxin-Cj2a) Interacting with Voltage-Gated Sodium Channel Subtype Na(V)1.4
title Molecular Surface of JZTX-V (β-Theraphotoxin-Cj2a) Interacting with Voltage-Gated Sodium Channel Subtype Na(V)1.4
title_full Molecular Surface of JZTX-V (β-Theraphotoxin-Cj2a) Interacting with Voltage-Gated Sodium Channel Subtype Na(V)1.4
title_fullStr Molecular Surface of JZTX-V (β-Theraphotoxin-Cj2a) Interacting with Voltage-Gated Sodium Channel Subtype Na(V)1.4
title_full_unstemmed Molecular Surface of JZTX-V (β-Theraphotoxin-Cj2a) Interacting with Voltage-Gated Sodium Channel Subtype Na(V)1.4
title_short Molecular Surface of JZTX-V (β-Theraphotoxin-Cj2a) Interacting with Voltage-Gated Sodium Channel Subtype Na(V)1.4
title_sort molecular surface of jztx-v (β-theraphotoxin-cj2a) interacting with voltage-gated sodium channel subtype na(v)1.4
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113750/
https://www.ncbi.nlm.nih.gov/pubmed/25055801
http://dx.doi.org/10.3390/toxins6072177
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