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      Biological and Proteolytic Variation in the Venom of Crotalus scutulatus scutulatus from Mexico

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          Abstract

          Rattlesnake venoms may be classified according to the presence/absence and relative abundance of the neurotoxic phospholipases A 2 s (PLA 2 s), such as Mojave toxin, and snake venom metalloproteinases (SVMPs). In Mexico, studies to determine venom variation in Mojave Rattlesnakes ( Crotalus scutulatus scutulatus) are limited and little is known about the biological and proteolytic activities in this species. Tissue (34) and venom (29) samples were obtained from C. s. scutulatus from different locations within their distribution in Mexico. Mojave toxin detection was carried out at the genomic (by PCR) and protein (by ELISA) levels for all tissue and venom samples. Biological activity was tested on representative venoms by measuring LD 50 and hemorrhagic activity. To determine the approximate amount of SVMPs, 15 venoms were separated by RP-HPLC and variation in protein profile and proteolytic activity was evaluated by SDS-PAGE ( n = 28) and Hide Powder Azure proteolytic analysis ( n = 27). Three types of venom were identified in Mexico which is comparable to the intraspecific venom diversity observed in the Sonoran Desert of Arizona, USA: Venom Type A (∼Type II), with Mojave toxin, highly toxic, lacking hemorrhagic activity, and with scarce proteolytic activity; Type B (∼Type I), without Mojave toxin, less toxic than Type A, highly hemorrhagic and proteolytic; and Type A + B, containing Mojave toxin, as toxic as venom Type A, variable in hemorrhagic activity and with intermediate proteolytic activity. We also detected a positive correlation between SVMP abundance and hemorrhagic and proteolytic activities. Although more sampling is necessary, our results suggest that venoms containing Mojave toxin and venom lacking this toxin are distributed in the northwest and southeast portions of the distribution in Mexico, respectively, while an intergradation in the middle of both zones is present.

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          Enzymatic toxins from snake venom: structural characterization and mechanism of catalysis.

          Snake venoms are cocktails of enzymes and non-enzymatic proteins used for both the immobilization and digestion of prey. The most common snake venom enzymes include acetylcholinesterases, l-amino acid oxidases, serine proteinases, metalloproteinases and phospholipases A(2) . Higher catalytic efficiency, thermal stability and resistance to proteolysis make these enzymes attractive models for biochemists, enzymologists and structural biologists. Here, we review the structures of these enzymes and describe their structure-based mechanisms of catalysis and inhibition. Some of the enzymes exist as protein complexes in the venom. Thus we also discuss the functional role of non-enzymatic subunits and the pharmacological effects of such protein complexes. The structures of inhibitor-enzyme complexes provide ideal platforms for the design of potent inhibitors which are useful in the development of prototypes and lead compounds with potential therapeutic applications. © 2011 The Authors Journal compilation © 2011 FEBS.
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            Cladistic biogeography of the Mexican transition zone

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              Key events in microvascular damage induced by snake venom hemorrhagic metalloproteinases.

              Hemorrhage is one of the most significant effects in envenomings induced by viperid snakebites. Damage to the microvasculature, induced by snake venom metalloproteinases (SVMPs), is the main event responsible for this effect. The precise mechanism by which SVMPs disrupt the microvasculature has remained elusive, although recent developments provide valuable clues to deciphering the details of this pathological effect. The main targets of hemorrhagic SVMPs are components of basement membrane (BM) and surrounding extracellular matrix (ECM), which provide mechanical stability to capillaries. P-III SVMPs, comprising disintegrin-like and cysteine-rich domains in addition to the catalytic domain, are more potent hemorrhagic toxins than P-I SVMPs, constituted only by the metalloproteinase domain. This is likely due to the presence of exosites in the additional domains, which contribute to the binding of SVMPs to relevant targets in the microvasculature. Recent in vivo studies have shown that P-III SVMPs are preferentially located in microvessels. On the other hand, the structural determinants responsible for the different hemorrhagic potential of P-I SVMPs remain largely unknown, although backbone flexibility in a loop located near the active site is likely to play a role. Moreover, hemorrhagic and non-hemorrhagic SVMPs differ in their capacity to hydrolyze in vivo key BM proteins, such as type IV collagen and perlecan, as well as other ECM proteins, like types VI and XV collagens, which play a critical role by connecting BM components to perivascular fibrillar collagens. The evidence gathered support a two-step model for the pathogenesis of SVMP-induced hemorrhage: initially, hemorrhagic SVMPs bind to and hydrolyze components of the BM and associated extracellular matrix proteins that play a key role in the mechanical stability of BM. In conditions of normal blood flow in the tissues, such cleavage results in the weakening, distension and eventual disruption of capillary wall due to the action of biophysical forces operating in vivo. Copyright © 2011 Elsevier B.V. All rights reserved.
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                Author and article information

                Journal
                Toxins (Basel)
                Toxins (Basel)
                toxins
                Toxins
                MDPI
                2072-6651
                08 January 2018
                January 2018
                : 10
                : 1
                : 35
                Affiliations
                [1 ]Facultad de Ciencias Biológicas, Universdad Juárez del Estado de Durango, Av. Universidad s/n. Fracc. Filadelfia, C.P. 35010 Gómez Palacio, Dgo., Mexico; alessandro_53@ 123456hotmail.com (M.B.); gamaliel.cg@ 123456gmail.com (G.C.-G.); jjcg00@ 123456gmail.com (J.C.-G.)
                [2 ]Facultad de Ciencias Químicas, Universidad Juárez del Estado de Durango, Av. Artículo 123 s/n. Fracc. Filadelfia, Apartado Postal No. 51, C.P. 35010 Gómez Palacio, Dgo., Mexico
                [3 ]Instituto de Biotecnología, Universidad Nacional Autónoma de Mexico, Avenida Universidad 2001, Chamilpa, C.P. 62210 Cuernavaca, Mor., Mexico; neri@ 123456ibt.unam.mx (E.N.-C.); joserobertoponcelopez21@ 123456gmail.com (R.P.-L.); aolvera@ 123456ibt.unam.mx (A.O.-R.); alagon@ 123456ibt.unam.mx (A.A.)
                [4 ]Department of Biology, University of Central Florida, 4000 Central Florida Blvd., Orlando, FL 32816, USA; Jason.Strickland@ 123456ucf.edu
                [5 ]Department of Biological Sciences and Department of Forestry and Environmental Conservation, Clemson University, 190 Collings St., Clemson, SC 29634, USA; viper@ 123456clemson.edu
                [6 ]Instituto Clodomiro Picado, Facultad de Microbiología, Universidad de Costa Rica, San José 11501, Costa Rica; bruno.lomonte@ 123456ucr.ac.cr
                Author notes
                [* ]Correspondence: rebecapms@ 123456ujed.mx ; Tel.: +52-871-7158810
                Author information
                https://orcid.org/0000-0003-4098-7279
                https://orcid.org/0000-0003-1551-4584
                https://orcid.org/0000-0002-1927-7259
                https://orcid.org/0000-0002-2020-6992
                https://orcid.org/0000-0003-2419-6469
                Article
                toxins-10-00035
                10.3390/toxins10010035
                5793122
                29316683
                394947b9-5f9f-4991-b114-5fa2c0879b7e
                © 2018 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 (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 20 November 2017
                : 04 January 2018
                Categories
                Article

                Molecular medicine
                mojave rattlesnakes,mojave toxin,pla2s,svmps,venom phenotypes,hemorrhagic activity,crotalus scutulatus scutulatus individuals with type a, type a + b, and type b venoms were confirmed in mexico. proteolytic and biological activity shows high variation among individuals with a specific geographic pattern.

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