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==Contact Info==
=Welcome!=
[[Image:Profile_picture_OrsiKiraly.JPG|thumb|right|]]
[[Image:OKiraly_profile.jpg|thumb|230px|right|]]


*Orsolya Kiraly
==Orsolya Kiraly, PhD==
*Postdoctoral Associate, Engelward laboratory
*Department of Biological Engineering
*Massachusetts Institute of Technology
*77 Massachusetts Ave, Cambridge, MA
*Lab: 617-750-7335 (Room 16-760)
*[[Special:Emailuser/Orsolya Kiraly|Email me through OpenWetWare]]


==Education==
*'''Research Affiliate''', [http://web.mit.edu/engelward-lab/ Engelward Laboratory]
<!--Include info about your educational background-->
*[http://web.mit.edu/be/index.shtml Department of Biological Engineering]
* Ph.D., Pathobiochemistry,  [http://english.sote.hu/ Semmelweis University], [http://en.wikipedia.org/wiki/Budapest Budapest], Hungary, 2008
*[http://web.mit.edu/ Massachusetts Institute of Technology]
* B.S., Molecular Biology, [http://www.elte.hu/en Eötvös Loránd University], Budapest, Hungary, 2002
*okiraly AT mit DOT edu
 
*'''Research Scientist''', [http://smart.mit.edu/home.html Singapore-MIT Alliance for Research and Technology]
*1 CREATE Way #03-12, Singapore 138602
*okiraly AT smart DOT mit DOT edu
*http://sg.linkedin.com/in/okiraly
 
 
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 [http://openwetware.org/wiki/20.109%28F10%29 20.109 Laboratory Fundamentals of Biological Engineering] (core undergraduate course for bioengineering students at MIT). See some course material [http://openwetware.org/wiki/20.109%28F10%29:_Fall_2010_schedule here].
*Teaching Certificate from the [http://tll.mit.edu/ 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.
 
 
==Scientific projects==
[[Image:FYDR_pancreas_small.tif|thumb|300px|left|]]
 
===My current work is about genome rearrangements (large-scale mutations), which can lead to cancer===
 
I received my PhD for work on how mutations in [http://www.uniprot.org/uniprot/P00995 pancreatic trypsin inhibitor] cause inflammation.  In the [http://web.mit.edu/engelward-lab/ Engelward Lab], my work is aimed at [http://www.yourgenome.org/sis/gd/gd03.shtml genome rearrangements] in the pancreas ''in vivo''.


==Research interests==
Genome rearrangements are a hallmark of cancer cells. They can be [http://en.wikipedia.org/wiki/Deletion_%28genetics%29 deletions], [http://en.wikipedia.org/wiki/Chromosomal_inversion inversions] or [http://en.wikipedia.org/wiki/Gene_duplication duplications] that can drive cancer by activating [http://en.wikipedia.org/wiki/Oncogene oncogenes] or inactivating [http://en.wikipedia.org/wiki/Tumor_suppressor_gene tumor suppressor genes]. Rearrangements can form by [http://en.wikipedia.org/wiki/Homologous_recombination homologous recombination] (HR), which is [http://web.mit.edu/engelward-lab/hr_intro.htm an important DNA repair/tolerance mechanism] but [http://www.ncbi.nlm.nih.gov/pubmed/11250067 can lead to genetic changes].
'''My current work is about DNA damage and homologous recombination'''


I received my PhD for work on how rare mutations in [http://www.uniprot.org/uniprot/P00995 pancreatic trypsin inhibitor] contribute to chronic pancreatic inflammation. In the [http://web.mit.edu/engelward-lab/ Engelward lab], my current work is aimed at [http://en.wikipedia.org/wiki/Homologous_recombination homologous recombination] in the pancreas in vivo.
Using a [http://www.pnas.org/content/103/32/11862.long 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 [http://en.wikipedia.org/wiki/Gene%E2%80%93environment_interaction gene-environment interactions] and may be used to [http://www.ncbi.nlm.nih.gov/pubmed/9353182 identify people with a higher risk for cancer]. Further, we found that inflammation, [http://carcin.oxfordjournals.org/content/30/7/1073.long a major cancer risk factor], induces HR-driven rearrangements through increasing both [http://www.ncbi.nlm.nih.gov/pubmed/21387284 DNA damage] and [http://en.wikipedia.org/wiki/Regeneration_%28biology%29 regenerative proliferation].  


While mitotic homologous  recombination is [http://web.mit.edu/engelward-lab/hr_intro.htm an important DNA repair/tolerance mechanism], it can result in sequence rearrangements that can contribute to cancer.  I am investigating the effects of DNA damaging chemicals, radiation, cell proliferation and DNA repair on homologous recombination in the pancreas.  
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 [http://smart.mit.edu/ SMART] developing mitigators of inflammation-induced tissue injury.


The next question in my project is whether homologous recombination is induced by inflammation, [http://carcin.oxfordjournals.org/content/30/7/1073.long which is a major risk factor for cancer].


==Past projects==
==Past projects==
'''Functional effects of sequence variants in promoters, introns, and protein-coding regions'''
[[Image:Bench_BU.jpg|thumb|420px|right|]]
 
===Functional effects of sequence variants in promoters, introns, and protein-coding regions===
 
*In the laboratory of [http://dentalschool.bu.edu/research/molecular/sahin-toth.htm Miklos Sahin-Toth] at Boston University, I determined the functional effects of patient-derived mutations in [http://www.ihop-net.org/UniPub/iHOP/gs/92355.html 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 [http://digestive.niddk.nih.gov/ddiseases/pubs/pancreatitis/ pancreatic inflammation]. We found that signal peptide mutations [http://www.ncbi.nlm.nih.gov/pubmed/17274009 abolish the secretion of SPINK1] into pancreatic juice, and a set of coding region mutations cause misfolding of the protein which is then [http://www.ncbi.nlm.nih.gov/pubmed/17525091 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.


In the lab of [http://dentalschool.bu.edu/research/molecular/sahin-toth.htm Miklos Sahin-Toth] at Boston University, I was investigating the functional effects of mutations in SPINK1, the pancreatic secretory trypsin inhibitor. This inhibitor is an important line of defense against trypsin activity in the pancreas. It is important to inhibit any trypsin activity in the pancreas 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.
*As side projects in the Sahin-Toth Lab, I initiated testing the functional effects of [http://www.ncbi.nlm.nih.gov/pubmed/18978175 intronic mutations in SPINK1], and also tested a patient-derived mutation in [http://www.ihop-net.org/UniPub/iHOP/gs/91370.html cationic trypsinogen]. Autoactivation of [http://en.wikipedia.org/wiki/Trypsinogen trypsinogen] had been [http://www.ncbi.nlm.nih.gov/pubmed/16791840 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 [http://www.ncbi.nlm.nih.gov/pubmed/16542853 developed a novel expression system], which has been included in [http://link.springer.com/protocol/10.1007%2F978-1-61737-967-3_10 Methods in Molecular Biology].
We found that signal peptide mutations [http://www.ncbi.nlm.nih.gov/pubmed/17274009 abolish the secretion of SPINK1] into pancreatic juice, and coding region mutations cause misfolding of the protein which is [http://www.ncbi.nlm.nih.gov/pubmed/17525091 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.


[[Image:PIntE170K.jpg|thumb|140px|right|]]


At [http://english.sote.hu/ Semmelweis University] I was working in a team studying the functional effects of polymorphisms in the promoter of the D4 dopamine receptor gene. This gene was the first one to be investigated in psychiatric genetics association studies, and its polymorphisms are associated with several personality traits and disorders such as ADHD.
*At [http://english.sote.hu/ Semmelweis University] I was working in a team studying the [http://en.wikipedia.org/wiki/Dopamine_receptor_D4 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 [http://www.ncbi.nlm.nih.gov/pubmed/17171658 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 [http://www.ncbi.nlm.nih.gov/pubmed/17171658 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 [http://www.ncbi.nlm.nih.gov/pubmed/16723017 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 [http://en.wikipedia.org/wiki/Linkage_disequilibrium linkage disequilibrium] with the SNP.
However, the functional effects of promoter polymorphisms (and thus the molecular basis of these associations) was not clear. With a reporter gene assay, we found that [http://www.ncbi.nlm.nih.gov/pubmed/17171658 a duplication in the promoter decreases transcriptional efficiency], potentially influencing the number of receptor molecules and neurotransmission. However, the most widely studied SNP in the gene [http://www.ncbi.nlm.nih.gov/pubmed/16723017 had no effect on gene expression in our assay].  The apparent effect of this SNP in association studies is thus probably due to another variant which is in [http://en.wikipedia.org/wiki/Linkage_disequilibrium linkage disequilibrium] with the candidate SNP.


*My undergraduate thesis project at the [http://www.abc.hu/index.php?lang=en Agricultural Biotechnology Research Center] (in [http://en.wikipedia.org/wiki/G%C3%B6d%C3%B6ll%C5%91 Gödöllő], Hungary) was aimed at generating host factor independent mutants of the ''16-3'' phage [http://www.biomedsearch.com/nih/Phage-integrases-biology-applications/14687564.html integrase] by [http://en.wikipedia.org/wiki/Protein_engineering protein engineering]. Integrases catalyze [http://www.web-books.com/MoBio/Free/Ch8D7.htm site-specific recombination], which is harnessed in [http://en.wikipedia.org/wiki/Gene_targeting 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.


My undergraduate thesis project at the [http://www.abc.hu/index.php?lang=en Agricultural Biotechnology Research Center] (in [http://en.wikipedia.org/wiki/G%C3%B6d%C3%B6ll%C5%91 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.
This project and the excellent mentoring I received at ABC gave me strong foundations in laboratory techniques in molecular biology and an interest in DNA metabolism and recombination.


==Publications==
==Publications==
[[Image:Journals.jpg|thumb|320px|left|]]
===Research papers===
===Research papers===
See them [http://www.ncbi.nlm.nih.gov/pubmed?term=kiraly+o on PubMed]
See them [http://www.ncbi.nlm.nih.gov/pubmed?term=kiraly+o on PubMed]
Citation Index on [http://scholar.google.com.sg/citations?user=RJWT1hkAAAAJ&hl=en&oi=ao Google Scholar]


===Book chapters===
===Book chapters===
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, 2003, pp. 275-313.
Kiraly O, Guan L, Sahin-Toth M. [http://link.springer.com/protocol/10.1007%2F978-1-61737-967-3_10 '''Expression of Recombinant Proteins with Uniform N-Termini.'''] In: Ming-Qun X, Evans T  (Eds): [http://link.springer.com/book/10.1007/978-1-61737-967-3/page/1 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): [http://www.amazon.com/Chemical-Genomics-Series-Ferenc-Darvas/dp/0824754905 Chemical Genomics], Marcel Dekker Inc., New York, 2004, pp. 275-313.
 


Király O, Guan L, Sahin-Tóth M. Expression of recombinant proteins with uniform N termini using intein technology and aminopeptidase deficient Escherichia coli. In: Ming-Qun X, Evans T  (eds): Heterologous Protein Expression in E. coli, Methods in Molecular Biology, Springer/Humana Press, in press
==Education==
* Postdoc, [http://web.mit.edu/ MIT]
* Ph.D., Biochemistry,  [http://www.nytimes.com/2013/08/12/world/europe/medical-students-head-to-eastern-Europe.html?pagewanted=all&_r=0 Semmelweis University], [http://en.wikipedia.org/wiki/Budapest Budapest], Hungary, 2008; Thesis: [http://phd.sote.hu/mwp/phd_live/vedes/export/kiralyorsolya.e.pdf Pathobiochemistry of Pancreatic Secretory Tryprin Inhibitor (SPINK1)]; Thesis research at [http://www.bu.edu/ Boston University]
* B.S., Biology, [http://www.elte.hu/en ELTE], Budapest, Hungary, 2002; Thesis: Engineering the ''16-3'' Phage Integrase for Gene Targeting Applications; Thesis research at [http://www.abc.hu/en/ Agricultural Biotechnology Center]
* I was shaped greatly by an education at [http://www.apaczai.elte.hu/?fomenu=iskolankrol&cikk=bemutatkozas_en ELTE Apaczai High School]




==Bookmarks==
==Bookmarks==
[[Image:BNL_cartoon.jpg|thumb|300px|left|Just another lab door at [http://www.bnl.gov/world/ Brookhaven National Lab], where I was a user of the [http://www.bnl.gov/medical/nasa/nsrl_description.asp NASA Space Radiation Lab]]]
===Laboratory tools and resources===
*[http://www.qiagen.com/literature/benchguide/bg_pls_lit.aspx Qiagen bench guide]


===Laboratory tools and resources===
*[http://www.djblabcare.co.uk/djb/info/6/User_Tools Centrifuge calculator]
[http://www.qiagen.com/literature/benchguide/bg_pls_lit.aspx Qiagen bench guide]


[http://www.djblabcare.co.uk/djb/info/6/User_Tools Centrifuge calculator]
*[[Berglund:PCR_Additives]] A good list of PCR additives


[[Berglund:PCR_Additives]] A good list of PCR additives
*[http://www.genecards.org/ GeneCards]


[http://www.genecards.org/ GeneCards]
*[http://www.ihop-net.org/UniPub/iHOP/ Information Hyperlinked over Proteins]


[http://www.ihop-net.org/UniPub/iHOP/ Information Hyperlinked over Proteins]
*[http://vassarstats.net/index.html VassarStats: Online stats tool]


===Useful links===
===Useful links===
[http://monographs.iarc.fr/ENG/Classification/index.php Classification of carcinogens] according to the [http://www.iarc.fr/ International Agency for Research on Cancer]
*[http://cehs.mit.edu/ MIT Center for Environmental Health Sciences]
 
*[http://monographs.iarc.fr/ENG/Classification/index.php Classification of carcinogens] according to the [http://www.iarc.fr/ International Agency for Research on Cancer]
 
*[http://www.ewg.org/search Environmental Working Group]
 
*[http://ctd.mdibl.org/ The Comparative Toxicogenomics Database]
 
*[http://www.aacr.org/ American Association for Cancer Research]
 
*[http://odge.mit.edu/development/prodepot/ MIT Professional Development Video Portal]


[http://www.ewg.org/search Environmental Working Group]
*[http://web.mit.edu/mitpostdocs/resources.html MIT Postdoc Resources]


[http://ctd.mdibl.org/ The Comparative Toxicogenomics Database]
*[http://techtv.mit.edu/ MIT Tech TV]


[http://www.aacr.org/ American Association for Cancer Research]


===Good books===
===Good books===
[http://books.google.com/books?id=WYCJBzTxPywC&printsec=frontcover&dq=suffering+gene&hl=en&ei=0ciBTL3nG4P98Ab2vb2aAg&sa=X&oi=book_result&ct=result&resnum=1&ved=0CCUQ6AEwAA#v=onepage&q&f=false The Suffering Gene] is a very readable book about the various environmental exposures that can damage DNA
[[Image:Books_Central_Sq.jpg|thumb|200px|right|Books in [http://en.wikipedia.org/wiki/Central_Square_%28Cambridge%29 Central Square], [http://en.wikipedia.org/wiki/Cambridge,_Massachusetts Cambridge], my home for 7 years]]
 
*[http://books.google.com/books?id=WYCJBzTxPywC&printsec=frontcover&dq=suffering+gene&hl=en&ei=0ciBTL3nG4P98Ab2vb2aAg&sa=X&oi=book_result&ct=result&resnum=1&ved=0CCUQ6AEwAA#v=onepage&q&f=false The Suffering Gene] is a very readable book about the various environmental exposures that can damage DNA
 
*[http://books.google.com/books?id=5ziWNCqD7OEC&printsec=frontcover&dq=cancer+evolutionary&hl=en&ei=I8mBTPKHGoOC8gbav6H3AQ&sa=X&oi=book_result&ct=result&resnum=5&ved=0CEIQ6AEwBA Cancer, the Evolutionary Legacy] describes why we are susceptible to cancer even without environmental exposures
 
*[http://books.google.com/books?id=WGmVPGh7AOMC&printsec=frontcover&dq=correcting+the+blueprint+of+life&source=bl&ots=6XcQhpeXhL&sig=6B-9fzLtn4vZO6swtR-WTc8TgnA&hl=en&ei=IjmCTNCRJ8P-8Aa_hPWBAg&sa=X&oi=book_result&ct=result&resnum=1&ved=0CBIQ6AEwAA#v=onepage&q&f=false Correcting the Blueprint of Life: An Historical Account of the Discovery of DNA Repair Mechanisms] by [http://en.wikipedia.org/wiki/Errol_Friedberg Errol Friedberg] is a fascinating story of scientific discovery, great scientist personalities and the unpredictability of research


[http://books.google.com/books?id=5ziWNCqD7OEC&printsec=frontcover&dq=cancer+evolutionary&hl=en&ei=I8mBTPKHGoOC8gbav6H3AQ&sa=X&oi=book_result&ct=result&resnum=5&ved=0CEIQ6AEwBA Cancer, the Evolutionary Legacy] describes why we are susceptible to cancer even without environmental exposures
*[http://archive.org/details/artofscientifici00beve The Art of Scientific Investigation] by W.I.B. Beveridge, [http://mitpress.mit.edu/books/advice-young-investigator Advice for a Young Investigator] by [http://en.wikipedia.org/wiki/Santiago_Ram%C3%B3n_y_Cajal Santiago Ramon y Cajal], and [http://books.google.com.sg/books/about/From_Dream_to_Discovery.html?id=PD9DAAAAIAAJ&redir_esc=y From Dream to Discovery] by [http://en.wikipedia.org/wiki/Hans_Selye Hans Selye] are all excellent books on research


[http://books.google.com/books?id=WGmVPGh7AOMC&printsec=frontcover&dq=correcting+the+blueprint+of+life&source=bl&ots=6XcQhpeXhL&sig=6B-9fzLtn4vZO6swtR-WTc8TgnA&hl=en&ei=IjmCTNCRJ8P-8Aa_hPWBAg&sa=X&oi=book_result&ct=result&resnum=1&ved=0CBIQ6AEwAA#v=onepage&q&f=false Correcting the Blueprint of Life: An Historical Account of the Discovery of DNA Repair Mechanisms] by [http://en.wikipedia.org/wiki/Errol_Friedberg Errol C. Friedberg] is a fascinating story of scientific discovery, great scientist personalities and the unpredictability of research
*[http://books.google.com/books?id=8dSSt6Mrn6sC&printsec=frontcover&dq=at+the+end+of+an+age&source=bl&ots=QynHJAmmSs&sig=6TM1lalB77xQB69lGqQ7leewnU8&hl=en&ei=5jqCTMmMGYSclgfD_Yn5Dw&sa=X&oi=book_result&ct=result&resnum=2&sqi=2&ved=0CCIQ6AEwAQ#v=onepage&q&f=false At the End of an Age] by historian [http://en.wikipedia.org/wiki/John_Lukacs 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 [http://www.theamericanscholar.org/putting-man-before-descartes/ here]


[http://books.google.com/books?id=8dSSt6Mrn6sC&printsec=frontcover&dq=at+the+end+of+an+age&source=bl&ots=QynHJAmmSs&sig=6TM1lalB77xQB69lGqQ7leewnU8&hl=en&ei=5jqCTMmMGYSclgfD_Yn5Dw&sa=X&oi=book_result&ct=result&resnum=2&sqi=2&ved=0CCIQ6AEwAQ#v=onepage&q&f=false At the End of an Age] by historian [http://en.wikipedia.org/wiki/John_Lukacs 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 [http://www.theamericanscholar.org/putting-man-before-descartes/ here]
*Also by Lukacs, [http://www.staugustine.net/Confessions%20of%20an%20original%20sinner.htm Confessions of an Original Sinner] is a rich account of a journey through very different places and times, full of sharp observations


===Miscellaneous===
===Miscellaneous===
[http://www.sciencedaily.com/news/plants_animals/new_species/ New animal species] are being discovered to this day, the latest being [http://news.nationalgeographic.com/news/2010/09/100901-tarzan-chameleon-tarzanville-forest-science-environment/ the Tarzan chameleon]
*[http://www.sciencedaily.com/news/plants_animals/new_species/ New animal species] are being discovered to this day!


Read about which [http://en.wikipedia.org/wiki/List_of_Hungarians#Scientists_and_inventors Hungarian or Hungarian-born scientists] gave the world the [http://en.wikipedia.org/wiki/L%C3%A1szl%C3%B3_B%C3%ADr%C3%B3 ballpoint pen], [http://en.wikipedia.org/wiki/Dennis_Gabor holography], [http://en.wikipedia.org/wiki/Andrew_Grove Intel], [http://en.wikipedia.org/wiki/Ern%C5%91_Rubik Rubik’s cube], [http://en.wikipedia.org/wiki/Albert_Szent-Gy%C3%B6rgyi vitamin C], [http://en.wikipedia.org/wiki/Hans_Selye stress], and the [http://en.wikipedia.org/wiki/Le%C3%B3_Szil%C3%A1rd nuclear chain reaction]
*Read about which [http://en.wikipedia.org/wiki/List_of_Hungarians#Scientists_and_inventors Hungarian or Hungarian-born scientists] gave the world the [http://en.wikipedia.org/wiki/L%C3%A1szl%C3%B3_B%C3%ADr%C3%B3 ballpoint pen], [http://en.wikipedia.org/wiki/Dennis_Gabor holography], [http://en.wikipedia.org/wiki/Andrew_Grove Intel], [http://en.wikipedia.org/wiki/Ern%C5%91_Rubik Rubik’s cube], [http://en.wikipedia.org/wiki/Albert_Szent-Gy%C3%B6rgyi vitamin C], [http://en.wikipedia.org/wiki/Hans_Selye stress], and the [http://en.wikipedia.org/wiki/Le%C3%B3_Szil%C3%A1rd nuclear chain reaction]

Revision as of 21:28, 4 April 2014

Welcome!

Orsolya Kiraly, PhD


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.


Scientific projects

My current work is about genome rearrangements (large-scale mutations), which can lead to cancer

I received my PhD for work on how mutations in pancreatic trypsin inhibitor cause inflammation. In the Engelward Lab, my work is aimed at genome rearrangements in the pancreas in vivo.

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.


Past projects

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.


Publications

Research papers

See them on PubMed

Citation Index on Google Scholar

Book chapters

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.


Education


Bookmarks

Just another lab door at Brookhaven National Lab, where I was a user of the NASA Space Radiation Lab

Laboratory tools and resources

Useful links


Good books

Books in Central Square, Cambridge, my home for 7 years
  • The Suffering Gene is a very readable book about the various environmental exposures that can damage DNA
  • 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

Miscellaneous