Poster, 2017, ENG

Functional characterization of human phosphomannomutases by 31P-NMR

Andreotti G. 1, Liguori L. 1,3, Monticelli M. 1,2, Viscido G. 2, Cimmaruta C. 2, Citro V. 2, Cubellis M.V. 2

1 Institute of Biomolecular Chemistry - CNR, Pozzuoli-Naples, Italy (gandreotti@icb.cnr.it) 2 Department of Biology, University of Naples Federico II, Italy 3 Department of Environmental, Biological, and Pharmaceutical Sciences and Technologies, University of Campania "Luigi Vanvitelli", Italy

PMM2-CDG is caused by mutations in the gene PMM2 encoding phosphomannomutase2. Yet a paralogous enzyme exists in humans. PMM1 has an additional phosphatase activity and is able to hydrolyze glucose and mannose 1,6 bisphosphate. This latter activity is enhanced by increased concentrations of Inosine monophosphate (IMP). The specific role of the two enzymes in vivo is not fully understood and in particular the effect of PMM1 mutations on hypomorphic PMM2 has not been evaluated yet and IMP could play an important part. For this reason we believe that it is worth elucidating the functioning of PMM1. The first step towards protein N- or C-glycosylation requires the isomerization of mannose 6-phosphate into mannose 1-phosphate. In vitro however PMM1 and PMM2 are assayed measuring their phosphomutase activity in the opposite direction. Using 31P-NMR spectroscopy we tested both enzymes in the physiologically relevant direction, as well as the phosphatase activity of PMM1 in the presence or in the absence of IMP. We identified the residues which are responsible for the sensitivity of PMM1 to IMP and we modelled the interaction with the nucleotide using a docking program that consents full flexibility of the protein as well as the ligand.

Scientific CDG Symposium 2017, Leuven Institute for Irelan in Europe, 13-14/07/2017

Keywords

pmm2, congenital disorder glycosylation, 31P-NMR

CNR authors

Andreotti Giuseppina

CNR institutes

ICB – Istituto di chimica biomolecolare

ID: 379478

Year: 2017

Type: Poster

Creation: 2017-12-05 12:51:41.000

Last update: 2017-12-05 12:52:17.000

External links

OAI-PMH: Dublin Core

OAI-PMH: Mods

OAI-PMH: RDF

External IDs

CNR OAI-PMH: oai:it.cnr:prodotti:379478