Scientific Program

Conference Series Ltd invites all the participants across the globe to attend 17th Euro Biotechnology Congress Berlin, Germany.

Day 2 :

Keynote Forum

Dong-Hun Woo

NEXEL Co. Ltd., South Korea

Keynote: Drug screening and discovery using human pluripotent stem cell derived cells

Time : 09:00-09:45

OMICS International Euro Biotechnology 2017 International Conference Keynote Speaker Dong-Hun Woo photo

Dong-Hun Woo is a Chief Technology Officer (CTO) at NEXEL Co., Ltd. He received his PhD in Stem Cell Biology from Korea University. During this time, he worked on tissue regeneration through directed differentiation of human pluripotent stem cells into target cell types of the liver, pancreas, and brain. After PhD course, he initially extended his research into cancer stem cells, studying the molecular mechanisms underlying tumorigenicity of cancer stem cells in glioblastoma at the Lerner Research Institute of Cleveland Clinic in Cleveland, OH, USA. Then, he has his expertise in stem cell biology human pluripotent cell fate specification by bringing genome editing strategies to bear on induced pluripotent stem (IPS) cell models of human genetic diseases at the University of Pennsylvania, PA, USA. His current project involves the generation of functional cells from human pluripotent stem cells for drug screening and toxicity tests as Head of research programs at NEXEL Co., Ltd.


Drug-induced toxicity is a main reason for withdrawals of new drugs in late clinical phases and post-launch of the drugs. Thus, development of predictive in vitro assay for early toxicity evaluation is important for drug discovery process. Here, we show various kind of cells derived from human pluripotent stem cells (hPSCs) that could be used for early toxicity evaluation of drug candidates. From our inducing differentiation technology, we have routinely produced highly pure population (≥98%) of hepatocytes and cardiomyocytes from human embryonic stem cells (hESCs) and human induced pluripotent stem cells (hiPSCs). Furthermore, we optimized a culture condition of hPSC-derived functional cells suitable for toxicity tests in vitro, and we demonstrated the efficacy of our optimized hPSC-derived cell model for predicting toxicity against the several drugs. In conclusion, our hPSC-derived cell model could be a good alternative cell source for pre-clinical study such as predicting toxicity and efficacy test for the drugs, and translational research of disease cure.

Keynote Forum

Fuad Fares

University of Haifa, Israel

Keynote: Novel methods for designing long acting agonists and antagonists of glycoprotein hormones

Time : 09:45-10:30

OMICS International Euro Biotechnology 2017 International Conference Keynote Speaker Fuad Fares photo

Fuad Fares has completed his MSc and DSc studies at the Faculty of Medicine, Technion-Israel Institute of Technology, and Postdoctoral studies in Department of Molecular Biology and Pharmacology, School of Medicine, Washington University, St. Louis Missouri. He developed the Department of Molecular Genetics at Carmel Medical Center. He is an Associate Professor in Department of Human Biology, University of Haifa and Head of the Laboratory of Molecular Genetics. He has published more than 90 manuscripts in reputed journals and serving as a member of the Israel Council for Higher Education from last 14 years. He is the inventor of designing long-acting recombinant proteins and the initiator of Prolor Biotech Ltd.


One major issue regarding the clinical use of many peptides is their short half-life due to the rapid clearance from the circulation. To overcome this problem, we succeeded to ligate the signal sequence of O-linked oligosaccharides to the coding sequence of the hormones. The cassette gene that has been used contains the sequence of the carboxyl-terminal peptide of human chorionic gonadotropin b subunit. The CTP contains 28 amino acids with four O-linked oligosaccharide recognition sites. It was postulated that O-linked oligosaccharides add flexibility, hydrophilicity and stability to the protein. On the other hand, it was suggested that the four O-linked oligosaccharides play a significant role in preventing plasma clearance and thus increasing the half-life of the protein in circulation. Using this strategy, we succeeded to ligate the CTP to the coding sequence of follitropin, thyrotropin, erythropoietin, growth hormone and thus to increase the longevity and bioactivity of these proteins in-vivo. Interestingly, the new analogs of FSH and GH were found not immunogenic in human and it is already passed successfully clinical trials phase III and phase II respectively. Moreover, FSH long acting (ELONVA) was approved by the European Commission for treatment of fertility since 2010. In addition, our results indicated that long acting GH is not toxic in monkeys and the results from clinical trials phase I and phase II seem to be promising. Designing long acting peptides will diminish the cost of these drugs and perhaps reduce the number of injections in the clinical protocols. On the other hand, we found that deletion of N-linked oligosaccharides from hTSH subunits resulted in significant decreased in the bioactivity. Moreover, de-glycosylated variants of TSH compete with normal hTSH and human thyroid stimulating immunoglobulin in a dose dependent manner. Thus, this variant, behaves as potential antagonist, that may offer a novel therapeutic strategy in the treatment of Grave’s disease, the most generic form of hyperthyroidism. In conclusion, it was found that addition of O-linked oligosaccharides or deletion of N-linked oligosaccharides could be interesting strategy for designing new analogs of glycoprotein hormones