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Dr Vinayak Singh Senior Research Officer | TB and AMR BiologyVinayak (MSc-Biotechnology, PhD-Biochemistry) is an exceptionally skilled experimental biologist with >15 years of extensive drug discovery research experience. He has outstanding knowledge of the field of Microbiology, and of the related fields of Biochemistry as well as Microbial Genetics, Genomics and Physiology, especially as they apply to tuberculosis. Vinayak’s exceptional skills as a microbiologist with high-level expertise in antimicrobial drug discovery and development began from his experience at the CSIR-Central Drug Research Institute in Lucknow, India, where he completed a PhD degree in Biochemistry. Next, he joined the University of Cape Town (UCT) where he completed a very successful postdoctoral fellowship (2011-2016) in the lab of Prof. Valerie Mizrahi. He joined UCT’s Drug Discovery and Development Centre (H3D) in Jan 2017. He served as the lead researcher on studies that have been published in top international journals. Importantly, he has identified and validated >15 novel tuberculosis drug targets which have attracted significant interest in the global tuberculosis research community. His work is defined by the characteristics of scientific excellence and rigour as evidenced by his publications and awards. Being an artist of Molecular networks, Genomics and Metabolomics, his main interest is to deconvolute mechanism of action of potential compounds to fulfil a broad and acute interest in the discovery of new innovative drugs.
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Dr Kathryn J. Wicht Research Officer | Chemical Biology and Parasitology Kathryn received her Ph.D. in Chemistry from the University of Cape Town in 2015, where her research focused on high-throughput screening (HTS) for novel antimalarial compounds targeting the hemozoin formation pathway and medicinal chemistry optimization of the hit compounds. Computational modeling of the data, pooled with publically available HTS results, allowed for the development of Bayesian models to predict antiplasmodial activity and describe the common features of hemozoin inhibiting compounds. Synthesis and biological testing of the derivatives provided tool compounds for further understanding of the mechanism in which hemozoin inhibitors accumulate and result in the increase of free heme in the Plasmodium falciparum parasite’s digestive vacuole. |
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Dr John Woodland Research Officer | Chemical Biology and Medicinal Chemistry John is a chemical scientist with interdisciplinary research experience and a passionate interest in developing molecular strategies, such as treatments and tools, to tackle the scourge of infectious disease. His current role as a research officer at the Holistic Drug Discovery and Development (H3D) Centre, under the mentorship of Professor Kelly Chibale, involves conducting research in chemical biology and medicinal chemistry aspects of malaria drug discovery; specifically, mode-of-action studies and target deconvolution of hit compounds active against the human malaria parasite (Plasmodium falciparum), the medicinal chemistry optimisation of noncovalent and covalent inhibitors of Plasmodium kinases, and the integration of machine learning into workflows at the H3D Centre to reduce compound attrition rates.
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