4wtb Citations

Functional and structural studies of a Phospholipase A2-like protein complexed to zinc ions: Insights on its myotoxicity and inhibition mechanism.

Biochim Biophys Acta Gen Subj 1861 3199-3209 (2017)
Cited: 9 times
EuropePMC logo PMID: 27531710

Abstract

Background
Methods

Myographic and electrophysiological techniques were used to evaluate the inhibitory effect of zinc ions, isothermal titration calorimetry assays were used to measure the affinity between zinc ions and the toxin and X-ray crystallography was used to reveal details of this interaction.

Results

We demonstrated that zinc ions can effectively inhibit the toxin by the interaction with two different sites, which are related to two different mechanism of inhibition: preventing membrane disruption and impairing the toxin state transition. Furthermore, structural study presented here included an additional step in the current myotoxic mechanism improving the comprehension of the allosteric transition that PLA2-like proteins undergo to exert their function.

Conclusion

Our findings show that zinc ions are inhibitors of PLA2-like proteins and suggest two different mechanisms of inhibition for these ions.

Articles - 4wtb mentioned but not cited (3)

  1. Structural basis for phospholipase A2-like toxin inhibition by the synthetic compound Varespladib (LY315920). Salvador GHM, Gomes AAS, Bryan-Quirós W, Fernández J, Lewin MR, Gutiérrez JM, Lomonte B, Fontes MRM. Sci Rep 9 17203 (2019)
  2. PLA2-like proteins myotoxic mechanism: a dynamic model description. Borges RJ, Lemke N, Fontes MRM. Sci Rep 7 15514 (2017)
  3. Structural Basis of Lysosomal Phospholipase A2 Inhibition by Zn2. Bouley RA, Hinkovska-Galcheva V, Shayman JA, Tesmer JJG. Biochemistry 58 1709-1717 (2019)


Reviews citing this publication (1)

  1. Secreted Phospholipases A₂ from Animal Venoms in Pain and Analgesia. Zambelli VO, Picolo G, Fernandes CAH, Fontes MRM, Cury Y. Toxins (Basel) 9 E406 (2017)

Articles citing this publication (5)