Design of MHC I stabilizing peptides by agent-based exploration of sequence space

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Abstract

Identification of molecular features that determine peptide interaction with major histocompatibility complex I (MHC I) is essential for vaccine development. We have developed a concept for peptide design by combining an agent-based artificial ant system with artificial neural networks. A jury of feedforward networks classifies octapeptides that are recognized by mouse MHC I protein H-2Kb. Prediction accuracy yielded a correlation coefficient of 0.94. Peptides were designed in machina by the artificial ant system and tested in vitro for their MHC I stabilizing effect. The behavior of the search agents during the design process was controlled by the jury network. The experimentally determined prediction accuracy was 89% for the designed stabilizing and 95% for the non-stabilizing peptides. Novel H-2Kb stabilizing peptides were conceived that reveal extensions of known residue motifs. The combined network-agent system recognized context dependencies of residue positions. A diverse set of novel sequences exhibiting substantial activity was generated. © The Author 2007. Published by Oxford University Press. All rights reserved.

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Hiss, J. A., Bredenbeck, A., Losch, F. O., Wrede, P., Walden, P., & Schneider, G. (2007). Design of MHC I stabilizing peptides by agent-based exploration of sequence space. Protein Engineering, Design and Selection, 20(3), 99–108. https://doi.org/10.1093/protein/gzl054

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