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Molecular Evolution of a Peptide GPCR Ligand Driven by Artificial Neural Networks

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  • Sebastian Bandholtz
  • Jörg Wichard
  • Ronald Kühne
  • Carsten Grötzinger

Abstract

Peptide ligands of G protein-coupled receptors constitute valuable natural lead structures for the development of highly selective drugs and high-affinity tools to probe ligand-receptor interaction. Currently, pharmacological and metabolic modification of natural peptides involves either an iterative trial-and-error process based on structure-activity relationships or screening of peptide libraries that contain many structural variants of the native molecule. Here, we present a novel neural network architecture for the improvement of metabolic stability without loss of bioactivity. In this approach the peptide sequence determines the topology of the neural network and each cell corresponds one-to-one to a single amino acid of the peptide chain. Using a training set, the learning algorithm calculated weights for each cell. The resulting network calculated the fitness function in a genetic algorithm to explore the virtual space of all possible peptides. The network training was based on gradient descent techniques which rely on the efficient calculation of the gradient by back-propagation. After three consecutive cycles of sequence design by the neural network, peptide synthesis and bioassay this new approach yielded a ligand with 70fold higher metabolic stability compared to the wild type peptide without loss of the subnanomolar activity in the biological assay. Combining specialized neural networks with an exploration of the combinatorial amino acid sequence space by genetic algorithms represents a novel rational strategy for peptide design and optimization.

Suggested Citation

  • Sebastian Bandholtz & Jörg Wichard & Ronald Kühne & Carsten Grötzinger, 2012. "Molecular Evolution of a Peptide GPCR Ligand Driven by Artificial Neural Networks," PLOS ONE, Public Library of Science, vol. 7(5), pages 1-11, May.
  • Handle: RePEc:plo:pone00:0036948
    DOI: 10.1371/journal.pone.0036948
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    1. Midori Murakami & Tsutomu Kouyama, 2008. "Crystal structure of squid rhodopsin," Nature, Nature, vol. 453(7193), pages 363-367, May.
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