Orsolya Kiraly, PhD
- Research Affiliate, Engelward Laboratory
- Department of Biological Engineering
- Massachusetts Institute of Technology
- okiraly AT mit DOT edu
- Research Scientist, Singapore-MIT Alliance for Research and Technology
- 1 CREATE Way #03-12, Singapore 138602
- okiraly AT smart DOT mit DOT edu
Life scientist with 5+ years’ experience with cell-based assays and animal models, and the management of research projects across cultures and locations. Recognized for the ability to drive projects forward by efficient planning and coordination, anticipating problems, and skills in hands-on research work.
Proven record to improve processes and work independently and in teams to achieve expected results, demonstrated by developing and executing streamlined animal experimental protocol resulting in study finished 5 months ahead of time and at >50% reduced cost.
Research design, planning and execution
- Designed and successfully performed projects with bacterial, cell-based and animal models in 4 laboratories, resulting in 8 peer-reviewed scientific publications and 3 manuscripts in progress.
- Small animal handling & dosing, fluorescence microscopy, digital image processing & analysis, flow cytometry, recombinant DNA methods, protein expression & purification, cell culture and transfection, Western blotting, experimental design & data analysis, problem solving, accurate record keeping, laboratory management, teaching & mentoring, scientific writing, database management, goal oriented, strong organization, communication and time management skills, experienced with working under time pressure and fast-changing project priorities.
Teamwork, coordination and supervision
- Collaborated with engineers, technicians, clinical researchers, biologists, physicists, government lab administrators, financial administrators, and safety and animal facility personnel in a total of 8 projects
- Worked in teams ranging from 2 to 17 people from diverse backgrounds and cultures in Europe, the US and Asia
- Planned & coordinated 7 projects, 3 of them simultaneously
Communication, reporting and presentations
- Prepared written reports and research plans for principal investigator, funding agencies and collaborating laboratories
- Gave presentations to funding agencies, scientific audiences and the general public
Training and mentoring
- Trained coworkers in experimental & analysis methods which were adopted by animal research team
- Mentored an undergraduate student in research design and methods. The student was accepted into the graduate program of her choice and became a co-author on finished manuscript.
- Taught recombinant DNA technology at the undergraduate level in 20.109 Laboratory Fundamentals of Biological Engineering (core undergraduate course for bioengineering students at MIT). See some course material here.
- Teaching Certificate from the MIT Teaching and Learning Laboratory
Administration, record keeping and regulatory
- Developed SOPs for animal research team
- Planned, prepared and updated IACUC protocols. Animal study proceeded without delay throughout 5-year project.
- Successfully handled extensive administration load for repeated research runs at US government laboratory. All runs were completed within schedule and without problems.
My current work is about genome rearrangements (large-scale mutations), which can lead to cancer
Genome rearrangements are a hallmark of cancer cells. They can be deletions, inversions or duplications that can drive cancer by activating oncogenes or inactivating tumor suppressor genes. Rearrangements can form by homologous recombination (HR), which is an important DNA repair/tolerance mechanism but can lead to genetic changes.
Using a transgenic reporter mouse, we have found that the formation of HR-driven rearrangements is governed by an interplay of genes, environment and tissue physiology. This is an example of gene-environment interactions and may be used to identify people with a higher risk for cancer. Further, we found that inflammation, a major cancer risk factor, induces HR-driven rearrangements through increasing both DNA damage and regenerative proliferation.
These findings have led to the generation of an advanced reporter mouse for use in ongoing studies on HR-driven genetic changes, and a collaborative project at SMART developing mitigators of inflammation-induced tissue injury.
Functional effects of sequence variants in promoters, introns, and protein-coding regions
- In the laboratory of Miklos Sahin-Toth at Boston University, I determined the functional effects of patient-derived mutations in SPINK1, the pancreatic secretory trypsin inhibitor. Inhibition of trypsin activity by SPINK1 is important because trypsin activity can result in the activation of other digestive enzymes in a cascade reaction, which can lead to cell damage and pancreatic inflammation. We found that signal peptide mutations abolish the secretion of SPINK1 into pancreatic juice, and a set of coding region mutations cause misfolding of the protein which is then degraded intracellularly and is not secreted. In patients with these mutations, spontaneously activated trypsin is thus not inhibited by SPINK1, eventually resulting in autodigestion and inflammation.
- As side projects in the Sahin-Toth Lab, I initiated testing the functional effects of intronic mutations in SPINK1, and also tested a patient-derived mutation in cationic trypsinogen. Autoactivation of trypsinogen had been linked to pancreatic inflammation, and this mutation had been hypothesized to increase autoactivation. However, testing this hypothesis was challenging because we couldn’t express intact trypsinogen with the mutation. We therefore developed a novel expression system, which has been included in Methods in Molecular Biology.
- At Semmelweis University I was working in a team studying the D4 dopamine receptor gene. This gene was the first to be investigated in psychiatric genetics association studies, and its variants are associated with certain personality traits and disorders such as ADHD. However, the functional effects of these variants (and thus the molecular basis of phenotypic associations) were not clear. Using a reporter gene assay, we found that a duplication in the promoter decreases transcriptional efficiency, potentially influencing the abundance of receptor molecules and neurotransmission. However, the most widely studied SNP in the gene had no effect on gene expression in our assay. The apparent effect of this SNP in association studies may be due to another variant which is in linkage disequilibrium with the SNP.
- My undergraduate thesis project at the Agricultural Biotechnology Research Center (in Gödöllő, Hungary) was aimed at generating host factor independent mutants of the 16-3 phage integrase by protein engineering. Integrases catalyze site-specific recombination, which is harnessed in gene targeting. The excellent mentoring I received at ABC gave me a strong foundation in the laboratory techniques of molecular biology, and this project raised my interest in DNA metabolism and recombination.
See them on PubMed
Citation Index on Google Scholar
Kiraly O, Guan L, Sahin-Toth M. Expression of Recombinant Proteins with Uniform N-Termini. In: Ming-Qun X, Evans T (Eds): Heterologous Protein Expression in E. coli, Methods in Molecular Biology 705, Springer, Berlin, 2011, pp. 175-194.
Nemoda Z, Kiraly O, Barta C, Sasvari-Szekely M. Pharmacogenetic Aspects of Dopaminergic Neurotransmission-Related Gene Polymorphisms. In: Darvas F, Guttman A, Dormán G (Eds): Chemical Genomics, Marcel Dekker Inc., New York, 2004, pp. 275-313.
- Postdoc, MIT
- Ph.D., Biochemistry, Semmelweis University, Budapest, Hungary, 2008; Thesis: Pathobiochemistry of Pancreatic Secretory Tryprin Inhibitor (SPINK1); Thesis research at Boston University
- B.S., Biology, ELTE, Budapest, Hungary, 2002; Thesis: Engineering the 16-3 Phage Integrase for Gene Targeting Applications; Thesis research at Agricultural Biotechnology Center
- I was shaped greatly by an education at ELTE Apaczai High School
Laboratory tools and resources
- Berglund:PCR_Additives A good list of PCR additives
- The Suffering Gene is a very readable book about the various environmental exposures that can damage DNA
- Cancer, the Evolutionary Legacy describes why we are susceptible to cancer even without environmental exposures
- Correcting the Blueprint of Life: An Historical Account of the Discovery of DNA Repair Mechanisms by Errol Friedberg is a fascinating story of scientific discovery, great scientist personalities and the unpredictability of research
- The Art of Scientific Investigation by W.I.B. Beveridge, Advice for a Young Investigator by Santiago Ramon y Cajal, and From Dream to Discovery by Hans Selye are all excellent books on research
- At the End of an Age by historian John Lukacs is not a scientific book, but it contains a deeply informed reflection on the nature of historical and scientific knowledge. Read a shorter essay on this here
- Also by Lukacs, Confessions of an Original Sinner is a rich account of a journey through very different places and times, full of sharp observations
- New animal species are being discovered to this day!