Venom-derived peptide inhibitors of voltage-gated potassium channels.

作者: Raymond S. Norton , K. George Chandy

DOI: 10.1016/J.NEUROPHARM.2017.07.002

关键词:

摘要: Voltage-gated potassium channels play a key role in human physiology and pathology. Reflecting their importance, numerous channelopathies have been characterised that arise from mutations these or autoimmune attack on the channels. are also target of broad range peptide toxins venomous organisms, including sea anemones, scorpions, spiders, snakes cone snails; many peptides bind to with high potency selectivity. In this review we describe various classes block illustrate three-dimensional structures support channel blockade. The therapeutic opportunities afforded by highlighted. This article is part Special Issue entitled 'Venom-derived Peptides as Pharmacological Tools.'

参考文章(241)
Hai M. Nguyen, Eva M. Grössinger, Makoto Horiuchi, Kyle W. Davis, Lee-Way Jin, Izumi Maezawa, Heike Wulff, Differential Kv1.3, KCa3.1, and Kir2.1 expression in “classically” and “alternatively” activated microglia Glia. ,vol. 65, pp. 106- 121 ,(2017) , 10.1002/GLIA.23078
Fábio A. Nascimento, Danielle M. Andrade, Myoclonus epilepsy and ataxia due to potassium channel mutation (MEAK) is caused by heterozygous KCNC1 mutations Epileptic Disorders. ,vol. 18, pp. 135- 138 ,(2016) , 10.1684/EPD.2016.0859
Mark A. Corbett, Susannah T. Bellows, Melody Li, Renée Carroll, Silvana Micallef, Gemma L. Carvill, Candace T. Myers, Katherine B. Howell, Snezana Maljevic, Holger Lerche, Elena V. Gazina, Heather C. Mefford, Melanie Bahlo, Samuel F. Berkovic, Steven Petrou, Ingrid E. Scheffer, Jozef Gecz, Dominant KCNA2 mutation causes episodic ataxia and pharmacoresponsive epilepsy Neurology. ,vol. 87, pp. 1975- 1984 ,(2016) , 10.1212/WNL.0000000000003309
Ameet A. Chimote, Peter Hajdu, Alexandros M. Sfyris, Brittany N. Gleich, Trisha Wise-Draper, Keith A. Casper, Laura Conforti, Kv1.3 channels mark functionally competent CD8+ tumor infiltrating lymphocytes in head and neck cancer Cancer Research. ,vol. 77, pp. 53- 61 ,(2017) , 10.1158/0008-5472.CAN-16-2372
Elena Parrini, Carla Marini, Davide Mei, Anna Galuppi, Elena Cellini, Daniela Pucatti, Laura Chiti, Domenico Rutigliano, Claudia Bianchini, Simona Virdò, Dalila De Vita, Stefania Bigoni, Carmen Barba, Francesco Mari, Martino Montomoli, Tiziana Pisano, Anna Rosati, Clinical Study Group, Renzo Guerrini, None, Diagnostic Targeted Resequencing in 349 Patients with Drug‐Resistant Pediatric Epilepsies Identifies Causative Mutations in 30 Different Genes Human Mutation. ,vol. 38, pp. 216- 225 ,(2017) , 10.1002/HUMU.23149
Austin B. Schwartz, Anshika Kapur, Wentao Wang, Zhenbo Huang, Erminia Fardone, Goutam Palui, Hedi Mattoussi, Debra Ann Fadool, Margatoxin‐bound quantum dots as a novel inhibitor of the voltage‐gated ion channel Kv1.3 Journal of Neurochemistry. ,vol. 140, pp. 404- 420 ,(2017) , 10.1111/JNC.13891
Xénia Latypova, Naomichi Matsumoto, Cécile Vinceslas-Muller, Stéphane Bézieau, Bertrand Isidor, Noriko Miyake, Novel KCNB1 mutation associated with non-syndromic intellectual disability Journal of Human Genetics. ,vol. 62, pp. 569- 573 ,(2017) , 10.1038/JHG.2016.154
Karine Poirier, Géraldine Viot, Laura Lombardi, Clémence Jauny, Pierre Billuart, Thierry Bienvenu, Loss of Function of KCNC1 is associated with intellectual disability without seizures European Journal of Human Genetics. ,vol. 25, pp. 560- 564 ,(2017) , 10.1038/EJHG.2017.3
Hai M. Nguyen, Linda V. Blomster, Palle Christophersen, Heike Wulff, Potassium channel expression and function in microglia: Plasticity and possible species variations. Channels. ,vol. 11, pp. 305- 315 ,(2017) , 10.1080/19336950.2017.1300738
Tanima Bose, Ryan Lee, Aihua Hou, Louis Tong, K George Chandy, None, Tissue resident memory T cells in the human conjunctiva and immune signatures in human dry eye disease. Scientific Reports. ,vol. 7, pp. 45312- ,(2017) , 10.1038/SREP45312