A soluble inorganic pyrophosphatase from the cattle tick Rhipicephalus microplus capable of hydrolysing polyphosphates. Issue 2 (22nd December 2017)

• Record Type: Journal Article
• Authors: Cruz, C. S.; Costa, E. P.; Machado, J. A.; Silva, J. N.; Romeiro, N. C.; Moraes, J.; Silva, J. R.; Fonseca, R. N.; Vaz, I. S.; Logullo, C.; Campos, E.
• Is Part Of: Insect molecular biology. Volume 27:Issue 2(2018)
• Page Start: 260
• Page End: 267
• Publication Date: 2017-12-22
• Subjects: Arthropod -- Metabolism -- kinetic parameters; Insects -- Molecular aspects -- Periodicals; 595.7
• DOI: 10.1111/imb.12369
• Languages: English
• ISSNs: 0962-1075

Abstract

Abstract: Polyphosphates have been found in all cell types examined to date and play diverse roles depending on the cell type. In eukaryotic organisms, polyphosphates have been investigated mainly in mammalian cells, and only a few studies have addressed arthropods. Pyrophosphatases have been shown to regulate polyphosphate metabolism. However, these studies were restricted to trypanosomatids. Here we focus on the tick Rhipicephalus microplus, a haematophagous ectoparasite that is highly harmful to cattle. We produced a recombinant R. microplus pyrophosphatase (rRmPPase) with the aim of investigating its kinetic parameters using polyphosphates as substrate. Molecular docking assays of RmPPase with polyphosphates were also carried out. The kinetic and Hill coefficient parameters indicated that rRmPPase has a greater affinity, higher catalytic efficiency and increased cooperativity for sodium phosphate glass type 15 (polyP15 ) than for sodium tripolyphosphate (polyP3 ). Through molecular docking, we found that polyP3 binds close to the Mg 2+ atoms in the catalytic region of the protein, participating in their coordination network, whereas polyP15 interactions involve negatively charged phosphate groups and basic amino acid residues, such as Lys56, Arg58 and Lys193; polyP15 has a more favourable theoretical binding affinity than polyP3, thus supporting the kinetic data. This study shows, for the first time in arthropods, a pyrophosphatase with polyphosphatase activity, suggesting its participation in polyphosphate metabolism.