Open AccessStudy of intra–inter species protein–protein interactions for potential drug targets identification and subsequent drug design for Escherichia coli O104:H4 C277-11
Author(s) -
Shakhinur Islam Mondal,
Zabed Mahmud,
Montasir Elahi,
Arzuba Akter,
Nurnabi Azad Jewel,
Md. Mofizul Islam,
Sabiha Ferdous,
Taisei Kikuchi
Publication year - 2017
Publication title -
in silico pharmacology
Language(s) - English
Resource type - Journals
ISSN - 2193-9616
DOI - 10.1007/s40203-017-0021-5
Subject(s) - drug , in silico , escherichia coli , docking (animal) , druggability , computational biology , drug target , biology , drug discovery , identification (biology) , pharmacology , biochemistry , medicine , botany , nursing , gene
Protein–protein interaction (PPI) and host–pathogen interactions (HPI) proteomic analysis has been successfully practiced for potential drug target identification in pathogenic infections. In this research, we attempted to identify new drug target based on PPI and HPI computation approaches and subsequently design new drug against devastating enterohemorrhagic Escherichia coli O104:H4 C277-11 (Broad), which causes life-threatening food borne disease outbreak in Germany and other countries in Europe in 2011. Our systematic in silico analysis on PPI and HPI of E. coli O104:H4 was able to identify bacterial d -galactose-binding periplasmic and UDP- N -acetylglucosamine 1-carboxyvinyltransferase as attractive candidates for new drug targets. Furthermore, computational three-dimensional structure modeling and subsequent molecular docking finally proposed [3-(5-Amino-7-Hydroxy-[1,2,3]Triazolo[4,5- d ]Pyrimidin-2-Yl)- N -(3,5-Dichlorobenzyl)-Benzamide)] and (6-amino-2-[(1-naphthylmethyl)amino]-3,7-dihydro-8 H -imidazo[4,5-g]quinazolin-8-one) as promising candidate drugs for further evaluation and development for E. coli O104:H4 mediated diseases. Identification of new drug target would be of great utility for humanity as the demand for designing new drugs to fight infections is increasing due to the developing resistance and side effects of current treatments. This research provided the basis for computer aided drug design which might be useful for new drug target identification and subsequent drug design for other infectious organisms.