A Machine Learning Study on the Thermostability Prediction of (R)-ω-Selective Amine Transaminase from Aspergillus terreus.

Artificial intelligence technologies such as machine learning have been applied to protein engineering, with unique advantages in protein structure, function prediction, catalytic activity, and other issues in recent years. Screening better mutants is still a bottleneck in protein engineering. In th...

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Publicado en:BioMed Research International pp. 1 - 8
Autores principales: Jia, Li-li, Sun, Ting-ting, Wang, Yan, Shen, Yu
Formato: equations & formulas research tables/charts Journal Article
Publicado: Wiley-Blackwell 8/17/2021
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 8/17/2021
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        10.1155/2021/2593748
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        atl: A Machine Learning Study on the Thermostability Prediction of (R)-ω-Selective Amine Transaminase from Aspergillus terreus.
      aug:
        au:
          Jia, Li-li
          Sun, Ting-ting
          Wang, Yan
          Shen, Yu
        affil: School of Science, School of Big Data, Zhejiang University of Science and Technology, Hangzhou 310008, China
      sug:
        subj:
          Machine Learning
          Aspergillus
          Aminotransferases
          Temperature
          Prediction Models
          Artificial Intelligence
          Sequence Analysis
          Mutation
          Signal Processing, Computer Assisted
          Enzymes
          Diffusion of Innovation
          Amino Acids
          Algorithms
      ab: Artificial intelligence technologies such as machine learning have been applied to protein engineering, with unique advantages in protein structure, function prediction, catalytic activity, and other issues in recent years. Screening better mutants is still a bottleneck in protein engineering. In this paper, a new sequence-activity relationship method was analyzed for its application in improving the thermal stability of Aspergillus terreus (R)-ω-selective amine transaminase. The experimental data from 6 single-point mutated enzymes were used as a learning dataset to build models and predict the thermostability of 26 mutants. Based on digital signal processing (DSP), this method digitized the amino acid sequence of proteins by fast Fourier transform (FFT) and then established the best model applying partial least squares regression (PLSR) to screen out all possible mutants, especially those with high performance. In protein engineering, the innovative sequence activity relationship (ISAR) method can make a reasonable prediction using limited experimental data and significantly reduce the experimental cost. The half-life ( T 1 / 2 ) of (R)-ω-transaminase was fitted with the amino acid sequence by the ISAR algorithm, resulting in an R 2 of 0.8929 and a cvRMSE of 4.89. At the same time, the mutants with higher T 1 / 2 than the existing ones were predicted, laying the groundwork for better (R)-ω-transaminase in the later stage. The ISAR algorithm is expected to provide a new technique for protein evolution and screening.
      pubtype: Academic Journal
      doctype:
        equations & formulas
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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