Our Group organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)
Google Scholar citation report
Citations : 3314

Journal of Biotechnology & Biomaterials received 3314 citations as per Google Scholar report

Indexed In
  • Index Copernicus
  • Google Scholar
  • Sherpa Romeo
  • Open J Gate
  • Genamics JournalSeek
  • Academic Keys
  • ResearchBible
  • China National Knowledge Infrastructure (CNKI)
  • Access to Global Online Research in Agriculture (AGORA)
  • Electronic Journals Library
  • RefSeek
  • Hamdard University
  • EBSCO A-Z
  • OCLC- WorldCat
  • SWB online catalog
  • Virtual Library of Biology (vifabio)
  • Publons
  • Geneva Foundation for Medical Education and Research
  • Euro Pub
  • ICMJE
Recommended Journals
Share This Page

Engineering bacteria for the discovery of potential therapeutic compounds against protein misfolding diseases

11th World Congress on Biotechnology and Biotech Industries Meet

Georgios Skretas

National Hellenic Research Foundation, Greece

ScientificTracks Abstracts: J Biotechnol Biomater

DOI: 10.4172/2155-952X.C1.052

Abstract
It has now been widely recognized that many incurable diseases with enormous socioeconomic impact such as Alzheimerâ??s disease, Parkinsonâ??s disease, type-2 diabetes etc., are initiated by a common mechanism; the misfolding of specific proteins. Here, we describe the use of engineered bacterial cells as a platform for the discovery of potential therapeutics against such protein misfolding diseases (PMDs). The topic of the described research is the application of molecular evolution approaches for the discovery of compounds that rescue the misfolding of PMD associated proteins. To achieve this, Escherichia coli cells are first engineered to biosynthesize large libraries of test compounds with high structural diversity. Then, the same cells are modified further so that they allow the identification of the rare molecules that correct the folding of particular misfoldingprone and PMD associated proteins (MisPs) with the use of a genetic screen. Lead compounds identified by this initial screen, are then subjected to more detailed evaluation by biochemical and biophysical methods of protein analysis and their ability to inhibit MisP induced pathogenicity is tested using appropriate human cell assays or in vivo models of the disease of interest. The molecules capable of rescuing the misfolding of the target MisP and of antagonizing its associated pathogenicity become drug candidates against the specific disease. We will describe our efforts to identify such â??pharmacological chaperonesâ? against the misfolding of the amyloid ?² (A?²) peptide and of certain carcinogenic misfolded variants of human p53, with the aim of developing potentially therapeutic compounds against Alzheimerâ??s disease and cancer, respectively.
Biography

Georgios Skretas was graduated from the School of Chemical Engineering of the National Technical University of Athens, Greece in 1998 and received his PhD in Chemical Engineering from Princeton University, USA in 2006. He has then joined the University of Texas at Austin, USA to carry out Postdoctoral research training under the guidance of Professor George Georgiou. Since 2009, he has been the Principal Investigator of the Laboratory of Enzyme & Synthetic Biotechnology at the Institute of Biology, Medicinal Chemistry & Biotechnology of the National Hellenic Research Foundation, Greece, where he currently holds the rank of Research Assistant Professor.

Email: gskretas@eie.gr

Top