Skip to Main content Skip to Navigation
Journal articles

Calibration of the dianionic phosphate group. Validation on the recognition site of the homodimeric enzyme phosphoglucose isomerase.

Abstract : We calibrate and validate the parameters necessary to represent the dianionic phosphate group (DPG) in molecular mechanics. DPG is an essential fragment of signaling biological molecules and protein‐binding ligands. It is a constitutive fragment of biosensors, which bind to the dimer interface of phosphoglucose isomerase (PGI), an intracellular enzyme involved in sugar metabolism, as well as an extracellular protein known as autocrine motility factor (AMF) closely related to metastasis formation. Our long‐term objective is to design DPG‐based biosensors with enhanced affinities for AMF/PGI cancer biomarker in blood. Molecular dynamics with polarizable potentials could be used toward this aim. This requires to first evaluate the accuracy of such potentials upon representing the interactions of DPG with its PGI ligands and tightly bound water molecules. Such evaluations are done by comparisons with high‐level ab initio quantum chemistry (QC) calculations. We focus on the Sum of Interactions Between Fragments Ab initio computed (SIBFA) polarizable molecular mechanics procedure. We present first the results of the DPG calibration. This is followed by comparisons between ΔE(SIBFA) and ΔE(QC) regarding bi‐molecular complexes of DPG with the main‐chain and side‐chain PGI residues, which bind to it in the recognition site. We then consider DPG complexes with an increasing number of PGI residues. The largest QC complexes encompass the entirety of the recognition site, with six structural water molecules totaling up to 211 atoms. A persistent and satisfactory agreement could be shown between ΔE(SIBFA) and ΔE(QC). These validations constitute an essential first step toward large‐scale molecular dynamics simulations of DPG‐based biosensors bound at the PGI dimer interface.
Document type :
Journal articles
Complete list of metadatas

https://hal.archives-ouvertes.fr/hal-02377726
Contributor : Jean-Philip Piquemal <>
Submitted on : Friday, November 27, 2020 - 8:33:54 AM
Last modification on : Friday, November 27, 2020 - 8:33:54 AM

Identifiers

Citation

M. Devillers, Jean-Philip Piquemal, L. Salmon, N. Gresh. Calibration of the dianionic phosphate group. Validation on the recognition site of the homodimeric enzyme phosphoglucose isomerase.. Journal of Computational Chemistry, Wiley, 2020, 41 (8), pp.839-854. ⟨10.1002/jcc.26134⟩. ⟨hal-02377726⟩

Share

Metrics

Record views

80