Brown Spider Venom Phospholipase-D Activity upon Different Lipid Substrates
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Data
2023-02-01
Autores
Chaves-Moreira, Daniele
Gremski, Luiza Helena
de Moraes, Fábio Rogério [UNESP]
Vuitika, Larissa
Wille, Ana Carolina Martins
Hernández González, Jorge Enrique [UNESP]
Chaim, Olga Meiri
Senff-Ribeiro, Andrea
Arni, Raghuvir Krishnaswamy [UNESP]
Veiga, Silvio Sanches
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Resumo
Brown spider envenomation results in dermonecrosis, characterized by an intense inflammatory reaction. The principal toxins of brown spider venoms are phospholipase-D isoforms, which interact with different cellular membrane components, degrade phospholipids, and generate bioactive mediators leading to harmful effects. The Loxosceles intermedia phospholipase D, LiRecDT1, possesses a loop that modulates the accessibility to the active site and plays a crucial role in substrate. In vitro and in silico analyses were performed to determine aspects of this enzyme’s substrate preference. Sphingomyelin d18:1/6:0 was the preferred substrate of LiRecDT1 compared to other Sphingomyelins. Lysophosphatidylcholine 16:0/0:0 was preferred among other lysophosphatidylcholines, but much less than Sphingomyelin d18:1/6:0. In contrast, phosphatidylcholine d18:1/16:0 was not cleaved. Thus, the number of carbon atoms in the substrate plays a vital role in determining the optimal activity of this phospholipase-D. The presence of an amide group at C2 plays a key role in recognition and activity. In silico analyses indicated that a subsite containing the aromatic residues Y228 and W230 appears essential for choline recognition by cation-π interactions. These findings may help to explain why different cells, with different phospholipid fatty acid compositions exhibit distinct susceptibilities to brown spider venoms.
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brown spider, Loxosceles intermedia, phospholipase-D substrate, phospholipids, recombinant toxin, venom
Como citar
Toxins, v. 15, n. 2, 2023.