Esterase 2 as a fluorescent biosensor for the detection of organophosphorus compounds: docking and electronic insights from molecular dynamics

ABSTRACT Organophosphorus compounds (OP) are mainly used in agriculture as pesticides. Unfortunately, each year many rural workers are intoxicated by these compounds and, many times, the diagnosis of the exact molecule causing the intoxication can be tardy, exposing the patients to a huge risk of death. One way of preventing this delay is the use of enzymatic biosensors like the enzyme Esterase 2 from Alicyclobacillus acidocaldarius (AaEST2), which is an efficient fluorescent biosensor for OP identification. However, although this enzyme has been well studied experimentally, the complete understanding of the energy transfer processes that occur between AaEST2 and OPs is still obscure, making it difficult the accurate identification of the OP. In order to better understand this process, we applied in this work molecular docking and molecular dynamics studies, together with the Förster fluorescence resonance energy transfer (FRET) theory, to achieve a better understanding of the fluorescence profiles that are described in the literature and correlate them to individual OPs. Our results suggest that the pesticides chlorpyrifos, diazinon, parathion and paraoxon are all capable of quenching the residue Trp85 from AaEST2, triggering fluorescence. This supports our hypothesis that AaEST2 can be used as a fluorescent biosensor for the detection of organophosphorus compounds.

[1]  Th. Förster Energiewanderung und Fluoreszenz , 1946 .

[2]  G. Weber,et al.  Ultraviolet fluorescence of the aromatic amino acids. , 1957, The Biochemical journal.

[3]  H. Berendsen,et al.  Molecular dynamics with coupling to an external bath , 1984 .

[4]  Rahman,et al.  Molecular-dynamics study of atomic motions in water. , 1985, Physical review. B, Condensed matter.

[5]  D. Quinn,et al.  Acetylcholinesterase: enzyme structure, reaction dynamics, and virtual transition states , 1987 .

[6]  T. Darden,et al.  Particle mesh Ewald: An N⋅log(N) method for Ewald sums in large systems , 1993 .

[7]  Berk Hess,et al.  LINCS: A linear constraint solver for molecular simulations , 1997 .

[8]  T. N. Bhat,et al.  The Protein Data Bank , 2000, Nucleic Acids Res..

[9]  G. Manco,et al.  The crystal structure of a hyper-thermophilic carboxylesterase from the archaeon Archaeoglobus fulgidus. , 2001, Journal of molecular biology.

[10]  Wilfred F. van Gunsteren,et al.  An improved GROMOS96 force field for aliphatic hydrocarbons in the condensed phase , 2001, J. Comput. Chem..

[11]  Gerrit Groenhof,et al.  GROMACS: Fast, flexible, and free , 2005, J. Comput. Chem..

[12]  René Thomsen,et al.  MolDock: a new technique for high-accuracy molecular docking. , 2006, Journal of medicinal chemistry.

[13]  M. Parrinello,et al.  Canonical sampling through velocity rescaling. , 2007, The Journal of chemical physics.

[14]  Eric Jakobsson,et al.  An improved united atom force field for simulation of mixed lipid bilayers. , 2009, The journal of physical chemistry. B.

[15]  Michael Hamel-Green,et al.  Organization for the Prohibition of Chemical Weapons , 2010 .

[16]  Pramod C. Nair,et al.  An Automated Force Field Topology Builder (ATB) and Repository: Version 1.0. , 2011, Journal of chemical theory and computation.

[17]  L. Perezgasga,et al.  Substitution of the Catalytic Metal and Protein PEGylation Enhances Activity and Stability of Bacterial Phosphotriesterase , 2012, Applied Biochemistry and Biotechnology.

[18]  K. Kuča,et al.  First principles calculations of thermodynamics and kinetic parameters and molecular dynamics simulations of acetylcholinesterase reactivators: can mouse data provide new insights into humans? , 2012, Journal of biomolecular structure & dynamics.

[19]  V. Vasić,et al.  Send Orders of Reprints at Reprints@benthamscience.net Acetylcholinesterase Inhibitors: Pharmacology and Toxicology , 2022 .

[20]  Sang J. Chung,et al.  Intrinsic Tryptophan Fluorescence in the Detection and Analysis of Proteins: A Focus on Förster Resonance Energy Transfer Techniques , 2014, International journal of molecular sciences.

[21]  Ferdinando Febbraio,et al.  Fluorescence Spectroscopy Approaches for the Development of a Real-Time Organophosphate Detection System Using an Enzymatic Sensor , 2015, Sensors.

[22]  K. Kuča,et al.  Computational Enzymology and Organophosphorus Degrading Enzymes: Promising Approaches Toward Remediation Technologies of Warfare Agents and Pesticides. , 2016, Current medicinal chemistry.

[23]  S. Caprasecca,et al.  Photoprotection and triplet energy transfer in higher plants: the role of electronic and nuclear fluctuations. , 2015, Physical chemistry chemical physics : PCCP.

[24]  K. Kuča,et al.  Organophosphorus degrading enzymes : Molecular basis and perspectives for enzymatic bioremediation of agrochemicals , 2017 .

[25]  Kamil Kuča,et al.  Enzimas degradantes de organofosforados: Base molecular e perspectivas para biorremediação enzimática de agroquímicos , 2017 .

[26]  Eugenio Vilanova,et al.  New insights on molecular interactions of organophosphorus pesticides with esterases. , 2017, Toxicology.

[27]  C. Curutchet,et al.  Can Förster Theory Describe Stereoselective Energy Transfer Dynamics in a Protein-Ligand Complex? , 2017, The journal of physical chemistry. B.