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Mapping possible interaction sites for crotoxin in CNF, a gamma PLA 2 inhibitor from Crotalus durissus terrificus rattle snake, using SPOT synthesis.
- Source :
-
Toxicon : official journal of the International Society on Toxinology [Toxicon] 2023 Oct; Vol. 234, pp. 107267. Date of Electronic Publication: 2023 Sep 01. - Publication Year :
- 2023
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Abstract
- Phospholipases A <subscript>2</subscript> (PLA <subscript>2</subscript> s) are main components of snake venoms. Several snake species possess endogenous PLA <subscript>2</subscript> inhibitors in their circulating blood, which are generally known as sbPLIs (an acronym for snake blood phospholipase A <subscript>2</subscript> inhibitors). The sbPLIs are categorized in three classes (alpha, beta or gamma) depending on the existence of distinguishing protein domains in their structure. The Crotalus durrissus terrificus venom has a highly neurotoxic PLA <subscript>2</subscript> - crotoxin (CTX) - in its composition and the self-protection of the snake is mainly ensured by a sbĪ³PLI named CNF (standing for Crotalusneutralizing factor). In an attempt to find smaller molecules able to inhibit the catalytic activity of CTX, in the present study we used linear peptide arrays to identify CNF segments possibly involved in the interaction with the toxin. Five reacting segments were identified as possible interacting regions. The target peptides were synthesized and located in the in silico CNF structure. Although all of them are exposed to the solvent, high concentrations were needed to inhibit the PLA <subscript>2</subscript> activity of the whole venom or CTX. Limitations of the methodology employed and particular characteristics of CTX inhibition by CNF are discussed.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2023 Elsevier Ltd. All rights reserved.)
Details
- Language :
- English
- ISSN :
- 1879-3150
- Volume :
- 234
- Database :
- MEDLINE
- Journal :
- Toxicon : official journal of the International Society on Toxinology
- Publication Type :
- Academic Journal
- Accession number :
- 37661064
- Full Text :
- https://doi.org/10.1016/j.toxicon.2023.107267