journal = "IEEE/ACM Transactions on Computational Biology and
Bioinformatics",
title = "Improving Recognition of Antimicrobial Peptides and
Target Selectivity through Machine Learning and Genetic
Programming",
year = "2015",
abstract = "Growing bacterial resistance to antibiotics is
spurring research on using naturally-occurring
antimicrobial peptides (AMPs) as templates for novel
drug design. While experimentalists mainly focus on
systematic point mutations to measure the effect on
antibacterial activity, the computational community
seeks to understand what determines such activity in a
machine learning setting. The latter seeks to identify
the biological signals or features that govern
activity. In this paper, we advance research in this
direction through a novel method that constructs and
selects complex sequence-based features which capture
information about distal patterns within a peptide.
Comparative analysis with state-of-the-art methods in
AMP recognition reveals our method is not only among
the top performers, but it also provides transparent
summaries of antibacterial activity at the sequence
level. Moreover, this paper demonstrates for the first
time the capability not only to recognise that a
peptide is an AMP or not but also to predict its target
selectivity based on models of activity against only
Gram-positive, only Gram-negative, or both types of
bacteria. The work described in this paper is a step
forward in computational research seeking to facilitate
AMP design or modification in the wet laboratory.",