Peptides Selected Using Phage Library Variants, Effectively Inhibit Trypanosoma cruzi Infection


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Abstract

Four peptide sequences characterized by high content of hydrophobic, charged, and polar amino acids were obtained from 23 clones of M13 phage. Peptides P2 and P4 exhibited highest binding affinity for immobilized trypomastigotes. The inhibitory effects of peptides seemed to be due to blockade of certain epitopes on T. cruzi surface proteins responsible for interactions with the respective receptors of host cells.

About the authors

Yu. E. Kleshchenko

Department of Microbiology and Virology, Medical Institute, Peopleэs Friendship University of Russia

Author for correspondence.
Email: ykleschenko@gmail.com
Russian Federation, Moscow

A. V. Zhigunova

Department of Microbiology and Virology, Medical Institute, Peopleэs Friendship University of Russia

Email: ykleschenko@gmail.com
Russian Federation, Moscow

M. V. Dalin

Department of Microbiology and Virology, Medical Institute, Peopleэs Friendship University of Russia

Email: ykleschenko@gmail.com
Russian Federation, Moscow

V. Melnikov

Laboratory of Molecular Biology, School of Medicine, University of Colima

Email: ykleschenko@gmail.com
Mexico, Colima

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