Cancer biology/bioinformatics, RNA Biology, Nuclear export pathways, Genomics, RNA-protein interaction, Molecular chaperones, Drug discovery, Infectious diseases, Molecular toxicology, Protein-protein interaction, Epigenetics
Analytical Research Scientist with many years of educational and hands-on experience in experimental research and data analysis. Detail-oriented and methodical professional successful in developing in-depth research projects. Hardworking professional with extensive training in cancer research, nucelear-cytoplasmic transport, RNA-protein interaction, genomics and protein-protein interaction. Reliable team player with excellent communication and problem-solving skills.
Cloning Immunofluorescence analysis RNA fluorescence in-situ hybridization (mRNA FISH) Cell/Tissue culture Cell transfection/transformation Protein purification and crystallization SDS-PAGE analysis and immunoblotting Nucleocytoplasmic Fractionation Luciferase reporter assay Cell viability assay Protein-protein interaction and immunoprecipitation PCR/RT-PCR
Cancer biology/bioinformatics, RNA Biology, Nuclear export pathways, Genomics, RNA-protein interaction, Molecular chaperones, Drug discovery, Infectious diseases, Molecular toxicology, Protein-protein interaction, Epigenetics
Doctoral fellow
Rhodes University, Grahamstown, South Africa : 2018-2022
Research tittle: The role of HOP/STIP1 in nuclear-cytoplasmic transport
Supervisor: Professor Adrienne Edkins
Postgraduate studies
Saarland University, Saarland Germany: 2014-2016
Identification of important physicochemical properties of antibiotics and antineoplastic drugs based on their gene ontology categories: a machine learning approach
Supervisor: Professor Dr. Volkhard Helms
Research Assistant
Chair of computational biology, University of Saarland: July-December,2016
Advisor Name: Professor Dr. Volkhard Helms
Project: Antineoplastics and Antibiotics drugs analysis in cancer
Student internship August-September, 2015
Dept. of Applied Bioinformatics, German Cancer Research Centre (DFKZ), Heidelberg, Germany
Advisor: Prof E. Adebiyi, Prof Benedikt Brors
Project: Assessment of plasmodium falciparum RNA pseudoridylate synthase (putative) as novel drug target
· Primer Design for PCR
· Cloning of Pseudouridylate synthase into peT28a plasmid vector
· Sequencing of cloned plasmid
Merck innovation center, Merck KGaA, Darmstadt, Germany June-December 2017
· Data gathering and resource person for the accelerator teams
Journal Publications
Workshop
•"Cancer Bioinformatics Tools," 9th December 2022 ICGEB course, Muğla Sıtkı Koçman University, Turkey
• Advanced Proteomics Workshop, 20th August 2018 – 22nd August 2018, at the University of the Witwatersrand (South Africa), by Prof Kathryn Lilley (University of Cambridge, UK), Prof Stephen Pennington (University College Dublin, Ireland), and Prof David Tabb (Stellenbosch)
• H3ABioNet Postgraduate Bioinformatics Workshop 21st April-26th May 2014, Covenant University Bioinformatics Research (CUBRe), Ota Nigeria
• "Applications of bioinformatics in modern molecular biology," 21st-25th October 2013: Organized by the International Centre For Genetic Engineering and Biotechnology(ICGEB), New Delhi, India
Antibacterial activity of excretions/secretions of Lucilia sericata against selected bacteria
Supervised by: Dr Helen Hopper, Northumbria University
Lucilia sericata is used for therapeutic purposes in the treatment of chronically infected wounds. The larva of this fly heals wounds via wound debridement, disinfection and stimulation of wound healing by excretion of antibacterial and growth-promoting substances. The project was aimed at studying the antibacterial properties of the excretions/secretions (ES) of L.sericata against Methicillin resistant staphylococcus aureus (MRSA), Escherichia coli, Bacillus cereus, Staphylococcus aureus, and Pseudomonas aeruginosa. Three bioassays were used: zone of inhibition, colony-forming unit, and turbidometric assay. ES was obtained using larvae that has been exposed to bacteria infested porcine tissue and also from larvae that had never been in contact with bacteria.
Determination of 3D-structure of C.japonicus Pectate Lyase10A by X-ray Crystallography
Supervised by: Prof Gary Black, Northumbria University
Cellvibrio japonicus is a good source of highly efficient Pel10A which are widely applied in industrial processes. E.coli is also an efficient expression host for production of large quantity of recombinant Pel10A. Application of X-ray crystallography in studying the 3D structure of the catalytic module of Pel10A provides more understanding of its catalytic features. This technique requires large amount of high-quality crystals of pel10A, and the experiment was aimed at expression, purification, characterization, and crystallization of the catalytic module of pel10A. E.coli was transformed with pET-28a plasmid containing Pectate lyase (Pel10A) gene. Biochemical assay, electrophoresis, and crystallization analysis were carried out on the expressed recombinant protein.
· Mentoring: Nine-Tenths Matric Mentoring Programme, Grahamstown, South Africa
· Newcastle city ambassador supporter for the London 2012 Olympics in Newcastle, United Kingdom