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1.
Biochimie ; 206: 105-115, 2023 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-36273763

RESUMO

Snake envenomation is an ongoing global health problem and tropical neglected disease that afflicts millions of people each year. The only specific treatment, antivenom, has several limitations that affects its proper distribution to the victims and its efficacy against local effects, such as myonecrosis. The main responsible for this consequence are the phospholipases A2 (PLA2) and PLA2-like proteins, such as BthTX-I from Bothrops jararacussu. Folk medicine resorts to plants such as Tabernaemontana catharinensis to palliate these and other snakebite effects. Here, we evaluated the effect of its root bark extract and one of its isolated compounds, 12-methoxy-4-methyl-voachalotine (MMV), against the in vitro paralysis and muscle damage induced by BthTX-I. Secondary and quaternary structures of BthTX-I were not modified by the interaction with MMV. Instead, this compound interacted in an unprecedented way with the region inside the toxin hydrophobic channel and promoted a structural change in Val31, loop 58-71 and Membrane Disruption Site. Thus, we hypothesize that MMV inhibits PLA2-like proteins by preventing entrance of fatty acid into the hydrophobic channel. These data may explain the traditional use of T. catharinensis extract and confirm MMV as a promising candidate to complement antivenom or a structural guide to develop more effective inhibitors.


Assuntos
Bothrops , Venenos de Crotalídeos , Tabernaemontana , Animais , Antivenenos/farmacologia , Antivenenos/química , Tabernaemontana/metabolismo , Fosfolipases A2/química , Venenos de Serpentes , Venenos de Crotalídeos/química , Bothrops/metabolismo
3.
Nat Methods ; 10(11): 1099-101, 2013 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-24037245

RESUMO

We describe an algorithm for phasing protein crystal X-ray diffraction data that identifies, retrieves, refines and exploits general tertiary structural information from small fragments available in the Protein Data Bank. The algorithm successfully phased, through unspecific molecular replacement combined with density modification, all-helical, mixed alpha-beta, and all-beta protein structures. The method is available as a software implementation: Borges.


Assuntos
Cristalografia/métodos , Dobramento de Proteína , Estrutura Terciária de Proteína , Algoritmos , Bases de Dados de Proteínas , Modelos Moleculares
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