Abstract

Antimicrobial peptides are ubiquitous molecules that form the innate immune system of organisms across all kingdoms of life. Despite their prevalence and early origins, they continue to remain potent natural antimicrobial agents. Antimicrobial peptides are therefore promising drug candidates in the face of overwhelming multi-drug resistance to conventional antibiotics. Over the past few decades, thousands of antimicrobial peptides have been characterized in vitro, and their efficacy data are now available in a multitude of public databases. Computational antimicrobial peptide design attempts typically use such data. However, utilizing heterogenous data aggregated from different sources presents significant drawbacks. In this report, we present a uniform dataset containing 20 antimicrobial peptides assayed against 30 organisms of Gram-negative, Gram-positive, mycobacterial, and fungal origin. We also present circular dichroism spectra for all antimicrobial peptides. We draw simple inferences from this data, and we discuss what characteristics are essential for antimicrobial peptide efficacy. We expect our uniform dataset to be useful for future projects involving computational antimicrobial peptide design.

Highlights

  • Antimicrobial peptides (AMPs) are essential components of the innate immune systems of a variety of organisms ranging from microbes to humans

  • We present a dataset containing 600 minimum inhibitory concentration (MIC) values obtained from testing 20 peptides against 30 diverse pathogens

  • Our data is qualitatively superior to aggregated, multi-source heterogeneous data found on antimicrobial peptide databases [3,28,29,30], and should be more suitable for training future AMP design algorithms

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Summary

A Uniform In Vitro Efficacy Dataset to Guide

Deepesh Nagarajan 1 , Tushar Nagarajan 2 , Neha Nanajkar 1 and Nagasuma Chandra 1,3, *. Received: 16 December 2018; Accepted: 1 February 2019; Published: 10 February 2019

Introduction
Data Description
Identifying Effective Peptides Based on MIC Data
Positively Charged Residues Are Associated with Increased Peptide Activity
Apolar Residues Are Associated with Increased Peptide Activity
Helicity Is Not Essential for Peptide Activity
Discussion
Computational Design and Selection of Antimicrobial Peptides
Antimicrobial Susceptibility Assays
Findings
Circular Dichroism Experiments

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