Literature DB >> 21939428

Venoms as a platform for human drugs: translating toxins into therapeutics.

Glenn F King1.   

Abstract

INTRODUCTION: An extraordinarily diverse range of animals have evolved venoms for predation, defence, or competitor deterrence. The major components of most venoms are peptides and proteins that are often protease-resistant due to their disulfide-rich architectures. Some of these toxins have become valuable as pharmacological tools and/or therapeutics due to their extremely high specificity and potency for particular molecular targets. There are currently six FDA-approved drugs derived from venom peptides or proteins. AREAS COVERED: This article surveys the current pipeline of venom-derived therapeutics and critically examines the potential of peptide and protein drugs derived from venoms. Emerging trends are identified, including an increasing industry focus on disulfide-rich venom peptides and the use of a broader array of molecular targets in order to develop venom-based therapeutics for treating a wider range of clinical conditions. EXPERT OPINION: Key technical advances in combination with a renewed industry-wide focus on biologics have converged to provide a larger than ever pipeline of venom-derived therapeutics. Disulfide-rich venom peptides obviate some of the traditional disadvantages of therapeutic peptides and some may be suitable for oral administration. Moreover, some venom peptides can breach the blood brain barrier and translocate across cell membranes, which opens up the possibility of exploiting molecular targets not previously accessible to peptide drugs.

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Year:  2011        PMID: 21939428     DOI: 10.1517/14712598.2011.621940

Source DB:  PubMed          Journal:  Expert Opin Biol Ther        ISSN: 1471-2598            Impact factor:   4.388


  153 in total

Review 1.  Latarcins: versatile spider venom peptides.

Authors:  Peter V Dubovskii; Alexander A Vassilevski; Sergey A Kozlov; Alexey V Feofanov; Eugene V Grishin; Roman G Efremov
Journal:  Cell Mol Life Sci       Date:  2015-08-19       Impact factor: 9.261

Review 2.  Peptide identification by tandem mass spectrometry with alternate fragmentation modes.

Authors:  Adrian Guthals; Nuno Bandeira
Journal:  Mol Cell Proteomics       Date:  2012-05-17       Impact factor: 5.911

3.  Proteomics and deep sequencing comparison of seasonally active venom glands in the platypus reveals novel venom peptides and distinct expression profiles.

Authors:  Emily S W Wong; David Morgenstern; Ehtesham Mofiz; Sara Gombert; Katrina M Morris; Peter Temple-Smith; Marilyn B Renfree; Camilla M Whittington; Glenn F King; Wesley C Warren; Anthony T Papenfuss; Katherine Belov
Journal:  Mol Cell Proteomics       Date:  2012-08-16       Impact factor: 5.911

4.  Fulditoxin, representing a new class of dimeric snake toxins, defines novel pharmacology at nicotinic ACh receptors.

Authors:  Chun Shin Foo; Chacko Jobichen; Varuna Hassan-Puttaswamy; Zoltan Dekan; Han-Shen Tae; Daniel Bertrand; David J Adams; Paul F Alewood; J Sivaraman; Selvanayagam Nirthanan; R Manjunatha Kini
Journal:  Br J Pharmacol       Date:  2020-02-09       Impact factor: 8.739

5.  Analgesic effect of novel Kunitz-type polypeptides of the sea anemone Heteractis crispa.

Authors:  V M Tabakmakher; O V Sintsova; O N Krivoshapko; E A Zelepuga; M M Monastyrnaya; E P Kozlovskaya
Journal:  Dokl Biochem Biophys       Date:  2015-05-05       Impact factor: 0.788

Review 6.  Trends in peptide drug discovery.

Authors:  Markus Muttenthaler; Glenn F King; David J Adams; Paul F Alewood
Journal:  Nat Rev Drug Discov       Date:  2021-02-03       Impact factor: 84.694

7.  Melt With This Kiss: Paralyzing and Liquefying Venom of The Assassin Bug Pristhesancus plagipennis (Hemiptera: Reduviidae).

Authors:  Andrew A Walker; Bruno Madio; Jiayi Jin; Eivind A B Undheim; Bryan G Fry; Glenn F King
Journal:  Mol Cell Proteomics       Date:  2017-01-27       Impact factor: 5.911

8.  Modulatory features of the novel spider toxin μ-TRTX-Df1a isolated from the venom of the spider Davus fasciatus.

Authors:  Fernanda C Cardoso; Zoltan Dekan; Jennifer J Smith; Jennifer R Deuis; Irina Vetter; Volker Herzig; Paul F Alewood; Glenn F King; Richard J Lewis
Journal:  Br J Pharmacol       Date:  2017-06-27       Impact factor: 8.739

Review 9.  The Molecular Basis of Toxins' Interactions with Intracellular Signaling via Discrete Portals.

Authors:  Adi Lahiani; Ephraim Yavin; Philip Lazarovici
Journal:  Toxins (Basel)       Date:  2017-03-16       Impact factor: 4.546

10.  The peptide Phα1β, from spider venom, acts as a TRPA1 channel antagonist with antinociceptive effects in mice.

Authors:  Raquel Tonello; Camilla Fusi; Serena Materazzi; Ilaria M Marone; Francesco De Logu; Silvia Benemei; Muryel C Gonçalves; Elisabetta Coppi; Celio J Castro-Junior; Marcus Vinicius Gomez; Pierangelo Geppetti; Juliano Ferreira; Romina Nassini
Journal:  Br J Pharmacol       Date:  2016-11-28       Impact factor: 8.739

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