Toxins 2013, 5(6), 1202-1218; doi:10.3390/toxins5061202

Computational Design of Peptide Ligands for Ochratoxin A

email, email and * email
Received: 2 May 2013; in revised form: 13 June 2013 / Accepted: 13 June 2013 / Published: 21 June 2013
(This article belongs to the Special Issue Recent Advances in Ochratoxins Research)
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: In this paper, we describe a peptide library designed by computational modelling and the selection of two peptide sequences showing affinity towards the mycotoxin, ochratoxin A (OTA). A virtual library of 20 natural amino acids was used as building blocks to design a short peptide library against ochratoxin A template using the de novo design program, LeapFrog, and the dynamic modelling software, FlexiDock. Peptide sequences were ranked according to calculated binding scores in their capacity to bind to ochratoxin A. Two high scoring peptides with the sequences N'-Cys-Ser-Ile-Val-Glu-Asp-Gly-Lys-C' (octapeptide) and N'-Gly-Pro-Ala-Gly-Ile-Asp-Gly-Pro-Ala-Gly-Ile-Arg-Cys-C' (13-mer) were selected for synthesis from the resulting database. These synthesized peptides were characterized using a microtitre plate-based binding assay and a surface plasmon resonance biosensor (Biacore 3000). The binding assay confirmed that both de novo designed peptides did bind to ochratoxin A in vitro. SPR analysis confirmed that the peptides bind to ochratoxin A, with calculated KD values of ~15.7 μM (13-mer) and ~11.8 μM (octamer). The affinity of the peptides corresponds well with the molecular modelling results, as the 13-mer peptide affinity is about 1.3-times weaker than the octapeptide; this is in accordance with the binding energy values modelled by FlexiDock. This work illustrates the potential of using computational modelling to design a peptide sequence that exhibits in vitro binding affinity for a small molecular weight toxin.
Keywords: ochratoxin A; mycotoxins; peptide; computational modelling; surface plasmon resonance; biosensor
PDF Full-text Download PDF Full-Text [782 KB, uploaded 21 June 2013 13:34 CEST]

Export to BibTeX |

MDPI and ACS Style

Heurich, M.; Altintas, Z.; Tothill, I.E. Computational Design of Peptide Ligands for Ochratoxin A. Toxins 2013, 5, 1202-1218.

AMA Style

Heurich M, Altintas Z, Tothill IE. Computational Design of Peptide Ligands for Ochratoxin A. Toxins. 2013; 5(6):1202-1218.

Chicago/Turabian Style

Heurich, Meike; Altintas, Zeynep; Tothill, Ibtisam E. 2013. "Computational Design of Peptide Ligands for Ochratoxin A." Toxins 5, no. 6: 1202-1218.

Toxins EISSN 2072-6651 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert