Structure, mechanism, and enantioselectivity shifting of lipase LipK107 with a simple way

Lujia Zhang, Bei Gao, Zuanning Yuan, Xiao He, Y. Adam Yuan, John Zhang, Dongzhi Wei

Research output: Contribution to journalArticle

Abstract

Because of the complex mechanisms of enzymatic reactions, no precise and simple method of understanding and controlling the chiral selectivity of enzymes has been developed. However, structure-based rational design is a powerful approach to engineering enzymes with desired catalytic activities. In this work, a simple, structure-based, large-scale in silico design and virtual screening strategy was developed and successfully applied to enzyme engineering. We first performed protein crystallization and X-ray diffraction to determine the structure of lipase LipK107, which is a novel family I.1 lipase displaying activity for both R and S isomers in chiral resolution reactions. The catalytic mechanism of family I.1, which includes LipK107, was ascertained first through comparisons of the sequences and structures of lipases from other families. The binding states of LipK107, including the energy and the conformation of complexes with the R and S enantiomers, have been evaluated by careful biocomputation to figure out the reason for the higher S selectivity. Based on this study, a simple strategy for manipulating the chiral selectivity by modulating a crucial distance in the enzyme-substrate complex and judging virtual mutations in silico is recommended. Then, a novel electrostatic interaction analysis protocol was used to design LipK107 mutants to validate our strategy. Both positive and negative mutations determined using this theoretical protocol have been implemented in wet experiments and were proved to produce the desired enantioselectivity, showing a 176% increase or 50% decrease in enantioselectivity as desired. Because of its accuracy and versatility, the strategy is promising for practical applications.

Original languageEnglish (US)
Pages (from-to)1183-1192
Number of pages10
JournalBiochimica et Biophysica Acta - Proteins and Proteomics
Volume1844
Issue number7
DOIs
StatePublished - 2014

Fingerprint

Enantioselectivity
Lipase
Enzymes
Computer Simulation
Mutation
Enantiomers
Crystallization
Coulomb interactions
Static Electricity
X-Ray Diffraction
Isomers
Conformations
Catalyst activity
Screening
X ray diffraction
Substrates
Proteins
Experiments

Keywords

  • Crystal structures
  • Enantiomer selectivity
  • Enzyme
  • LipK107
  • Rational design

ASJC Scopus subject areas

  • Biochemistry
  • Biophysics
  • Analytical Chemistry
  • Molecular Biology

Cite this

Structure, mechanism, and enantioselectivity shifting of lipase LipK107 with a simple way. / Zhang, Lujia; Gao, Bei; Yuan, Zuanning; He, Xiao; Adam Yuan, Y.; Zhang, John; Wei, Dongzhi.

In: Biochimica et Biophysica Acta - Proteins and Proteomics, Vol. 1844, No. 7, 2014, p. 1183-1192.

Research output: Contribution to journalArticle

Zhang, Lujia ; Gao, Bei ; Yuan, Zuanning ; He, Xiao ; Adam Yuan, Y. ; Zhang, John ; Wei, Dongzhi. / Structure, mechanism, and enantioselectivity shifting of lipase LipK107 with a simple way. In: Biochimica et Biophysica Acta - Proteins and Proteomics. 2014 ; Vol. 1844, No. 7. pp. 1183-1192.
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