Přehled o publikaci
2021
Stabilization of Haloalkane Dehalogenase Structure by Interfacial Interaction with Ionic Liquids
SHAPOSHNIKOVA, Anastasiia; Michal KUTY; Radka CHALOUPKOVÁ; Jiří DAMBORSKÝ; Ivana KUTA SMATANOVA et al.Basic information
Original name
Stabilization of Haloalkane Dehalogenase Structure by Interfacial Interaction with Ionic Liquids
Authors
SHAPOSHNIKOVA, Anastasiia; Michal KUTY; Radka CHALOUPKOVÁ; Jiří DAMBORSKÝ; Ivana KUTA SMATANOVA; Babak MINOFAR and Tanyana PRUDNIKOVA
Edition
Crystals, MDPI, 2021, 2073-4352
Other information
Language
English
Type of outcome
Article in a journal
Country of publisher
Switzerland
Confidentiality degree
is not subject to a state or trade secret
References:
Marked to be transferred to RIV
Yes
RIV identification code
RIV/00216224:14310/21:00122906
Organization
Přírodovědecká fakulta – Repository – Repository
UT WoS
EID Scopus
Keywords in English
haloalkane dehalogenase (HLD); ionic liquids (ILs); molecular dynamics (MD) simulations; protein stability; 2-hydroxyethylammonium acetate ([ETA][ACC]); 1-butyl-3-methylimidazolium methyl sulfate ([EMIM][CHS])
Links
LM2015047, research and development project. LM2018140, research and development project. RECETOX RI, large research infrastructures.
Changed: 9/6/2025 00:50, RNDr. Daniel Jakubík
Abstract
In the original language
Ionic liquids attracted interest as green alternatives to replace conventional organic solvents in protein stability studies. They can play an important role in the stabilization of enzymes such as haloalkane dehalogenases that are used for biodegradation of warfare agents and halogenated environmental pollutants. Three-dimensional crystals of haloalkane dehalogenase variant DhaA80 (T148L+G171Q+A172V+C176F) from Rhodococcus rhodochrous NCIMB 13064 were grown and soaked with the solutions of 2-hydroxyethylammonium acetate and 1-butyl-3-methylimidazolium methyl sulfate. The objective was to study the structural basis of the interactions between the ionic liquids and the protein. The diffraction data were collected for the 1.25 angstrom resolution for 2-hydroxyethylammonium acetate and 1.75 angstrom resolution for 1-butyl-3-methylimidazolium methyl sulfate. The structures were used for molecular dynamics simulations to study the interactions of DhaA80 with the ionic liquids. The findings provide coherent evidence that ionic liquids strengthen both the secondary and tertiary protein structure due to extensive hydrogen bond interactions.