Parallel Computations in the Development of Thermostable Lipase Mutants


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The advanced high performance computing methods are used to study the stability and conformational dynamics of the bacterial enzyme lipase LipA, its mutants, and the close homologous enzyme CLE whose substrate is polylactic acid-based plastics. From the analysis of the GPU molecular dynamics of native lipases and their mutants the amino acid residues whose point substitutions can markedly improve the thermostability of the enzymes under study without deteriorating their activity are determined.

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M. Kondratyev

Institute of Cell Biophysics

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Email: ma-ko@bk.ru
俄罗斯联邦, Pushchino

A. Kabanov

Institute of Cell Biophysics

Email: ma-ko@bk.ru
俄罗斯联邦, Pushchino

A. Samchenko

Institute of Cell Biophysics

Email: ma-ko@bk.ru
俄罗斯联邦, Pushchino

V. Komarov

Institute of Cell Biophysics

Email: ma-ko@bk.ru
俄罗斯联邦, Pushchino

N. Khechinashvili

Institute of Cell Biophysics

Email: ma-ko@bk.ru
俄罗斯联邦, Pushchino

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