Snake Venom: A Promising Source of Neurotoxins Targeting Voltage-Gated Potassium Channels

被引:7
作者
Alshammari, Altaf K. [1 ]
Abd El-Aziz, Tarek Mohamed [2 ,3 ]
Al-Sabi, Ahmed [1 ]
机构
[1] Amer Univ Middle East, Coll Engn & Technol, Egaila 54200, Kuwait
[2] Minia Univ, Fac Sci, Zool Dept, El Minia 61519, Egypt
[3] Univ Texas Hlth Sci Ctr San Antonio, Dept Cellular & Integrat Physiol, San Antonio, TX 78229 USA
关键词
BPTI-Kunitz polypeptides; CRISPs; dendrotoxins; Kv channels blockers; PLA(2) neurotoxins; presynaptic neurotoxins; SVSPs; snake venom; DORSAL-ROOT GANGLION; AMERICAN RATTLESNAKE VENOM; SITE-DIRECTED MUTAGENESIS; RICH SECRETORY PROTEIN; GREEN MAMBA VENOM; NAJA-ATRA VENOM; K+-CHANNEL; CRYSTAL-STRUCTURE; BETA-BUNGAROTOXIN; ALPHA-DENDROTOXIN;
D O I
10.3390/toxins16010012
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The venom derived from various sources of snakes represents a vast collection of predominantly protein-based toxins that exhibit a wide range of biological actions, including but not limited to inflammation, pain, cytotoxicity, cardiotoxicity, and neurotoxicity. The venom of a particular snake species is composed of several toxins, while the venoms of around 600 venomous snake species collectively encompass a substantial reservoir of pharmacologically intriguing compounds. Despite extensive research efforts, a significant portion of snake venoms remains uncharacterized. Recent findings have demonstrated the potential application of neurotoxins derived from snake venom in selectively targeting voltage-gated potassium channels (Kv). These neurotoxins include BPTI-Kunitz polypeptides, PLA2 neurotoxins, CRISPs, SVSPs, and various others. This study provides a comprehensive analysis of the existing literature on the significance of Kv channels in various tissues, highlighting their crucial role as proteins susceptible to modulation by diverse snake venoms. These toxins have demonstrated potential as valuable pharmacological resources and research tools for investigating the structural and functional characteristics of Kv channels.
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页数:35
相关论文
共 213 条
[1]   Snake Venoms in Drug Discovery: Valuable Therapeutic Tools for Life Saving [J].
Abd El-Aziz, Tarek Mohamed ;
Soares, Antonio Garcia ;
Stockand, James D. .
TOXINS, 2019, 11 (10)
[2]   A Rational Design of a Selective Inhibitor for Kv1.1 Channels Prevalent in Demyelinated Nerves That Improves Their Impaired Axonal Conduction [J].
Al-Sabi, Ahmed ;
Daly, Declan ;
Hoefer, Patrick ;
Kinsella, Gemma K. ;
Metais, Charles ;
Pickering, Mark ;
Herron, Caroline ;
Kaza, Seshu Kumar ;
Nolan, Kieran ;
Dolly, J. Oliver .
JOURNAL OF MEDICINAL CHEMISTRY, 2017, 60 (06) :2245-2256
[3]   Inhibition of the Nicotinic Acetylcholine Receptors by Cobra Venom α-Neurotoxins: Is There a Perspective in Lung Cancer Treatment? [J].
Alama, Angela ;
Bruzzo, Cristina ;
Cavalieri, Zita ;
Forlani, Alessandra ;
Utkin, Yuri ;
Casciano, Ida ;
Romani, Massimo .
PLOS ONE, 2011, 6 (06)
[4]   Fifty years of inactivation [J].
Aldrich, RW .
NATURE, 2001, 411 (6838) :643-644
[5]   THE CONCISE GUIDE TO PHARMACOLOGY 2021/22: Ion channels [J].
Alexander, Stephen P. H. ;
Mathie, Alistair ;
Peters, John A. ;
Veale, Emma L. ;
Striessnig, Jorg ;
Kelly, Eamonn ;
Armstrong, Jane F. ;
Faccenda, Elena ;
Harding, Simon D. ;
Pawson, Adam J. ;
Southan, Christopher ;
Davies, Jamie A. ;
Aldrich, Richard W. ;
Attali, Bernard ;
Baggetta, Austin M. ;
Becirovic, Elvir ;
Biel, Martin ;
Bill, Roslyn M. ;
Catterall, William A. ;
Conner, Alex C. ;
Davies, Paul ;
Delling, Markus ;
Di Virgilio, Francesco ;
Falzoni, Simonetta ;
Fenske, Stefanie ;
George, Chandy ;
Goldstein, Steve A. N. ;
Grissmer, Stephan ;
Ha, Kotdaji ;
Hammelmann, Verena ;
Hanukoglu, Israel ;
Jarvis, Mike ;
Jensen, AndersA ;
Kaczmarek, Leonard K. ;
Kellenberger, Stephan ;
Kennedy, Charles ;
King, Brian ;
Kitchen, Philip ;
Lynch, Joseph W. ;
Perez-Reyes, Edward ;
Plant, Leigh D. ;
Rash, Lachlan ;
Ren, Dejian ;
Salman, Mootaz M. ;
Sivilotti, Lucia G. ;
Smart, Trevor G. ;
Snutch, Terrance P. ;
Tian, Jinbin ;
Trimmer, James S. ;
Van den Eynde, Charlotte .
BRITISH JOURNAL OF PHARMACOLOGY, 2021, 178 :S157-S245
[6]   Snake Venom Peptides and Low Mass Proteins: Molecular Tools and Therapeutic Agents [J].
Almeida, J. R. ;
Resende, L. M. ;
Watanabe, R. K. ;
Carregari, V. C. ;
Huancahuire-Vega, S. ;
Caldeira, C. A. da S. ;
Coutinho-Neto, A. ;
Soares, A. M. ;
Vale, N. ;
Gomes, P. A. de C. ;
Marangoni, S. ;
Calderon, L. de A. ;
Da Silva, S. L. .
CURRENT MEDICINAL CHEMISTRY, 2017, 24 (30) :3254-3282
[7]   Harnessing snake venom phospholipases A2 to novel approaches for overcoming antibiotic resistance [J].
Almeida, Jose R. ;
Palacios, Antonio L. V. ;
Patino, Ricardo S. P. ;
Mendes, Bruno ;
Teixeira, Catia A. S. ;
Gomes, Paula ;
da Silva, Saulo L. .
DRUG DEVELOPMENT RESEARCH, 2019, 80 (01) :68-85
[8]  
Amir R, 1999, J NEUROSCI, V19, P8589
[9]   From Snake Venoms to Therapeutics: A Focus on Natriuretic Peptides [J].
Ang, Wei Fong ;
Koh, Cho Yeow ;
Kini, R. Manjunatha .
PHARMACEUTICALS, 2022, 15 (09)
[10]  
Armstrong Clay M, 2003, Sci STKE, V2003, pre10, DOI 10.1126/stke.2003.188.re10