User:Orsolya Kiraly: Difference between revisions

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


*Research Affiliate, [http://web.mit.edu/engelward-lab/ Engelward Laboratory]
==Orsolya Kiraly, PhD==
 
*'''Research Affiliate''', [http://web.mit.edu/engelward-lab/ Engelward Laboratory]
*[http://web.mit.edu/be/index.shtml Department of Biological Engineering]
*[http://web.mit.edu/be/index.shtml Department of Biological Engineering]
*[http://web.mit.edu/ Massachusetts Institute of Technology]
*[http://web.mit.edu/ Massachusetts Institute of Technology]
*77 Massachusetts Avenue 16-760, Cambridge, MA
*okiraly AT mit DOT edu
*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
*http://sg.linkedin.com/in/okiraly
http://www.linkedin.com/img/webpromo/btn_viewmy_160x25.png




==Education==
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.
<!--Include info about your educational background-->
 
* Ph.D., Biochemistry,  [http://english.sote.hu/ Semmelweis University], [http://en.wikipedia.org/wiki/Budapest Budapest], Hungary, 2008
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.
* B.S., Biology, [http://www.elte.hu/en ELTE], Budapest, Hungary, 2002
 
* I was shaped greatly by an education at [http://www.apaczai.elte.hu/?fomenu=iskolankrol&cikk=bemutatkozas_en ELTE Apaczai High School]
 
==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.




==Research interests==
==Scientific projects==
[[Image:MIT_origami.jpg|thumb|230px|left|]]
[[Image:FYDR_pancreas_small.tif|thumb|300px|left|]]


===My current work is about genome rearrangements (large-scale mutations), which can lead to cancer===
===My current work is about genome rearrangements (large-scale mutations), which can lead to cancer===
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==Past projects==
==Past projects==
[[Image:Bench_BU.jpg|thumb|300px|right|]]
[[Image:Bench_BU.jpg|thumb|420px|right|]]


===Functional effects of sequence variants in promoters, introns, and protein-coding regions===
===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 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 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.


*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].
*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].


[[Image:PIntE170K.jpg|thumb|120px|right|]]
[[Image:PIntE170K.jpg|thumb|140px|right|]]


*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 candidate SNP.
*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.


*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 [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.
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==Publications==
==Publications==
[[Image:Journals.jpg|thumb|320px|right|]]
[[Image:Journals.jpg|thumb|320px|left|]]


===Research papers===
===Research papers===
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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.
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://trove.nla.gov.au/work/16512919?q&versionId=21007644 Chemical Genomics], Marcel Dekker Inc., New York, 2003, pp. 275-313.
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.




==Teaching==
==Education==
 
* Postdoc, [http://web.mit.edu/ MIT]
*Lectures in [http://openwetware.org/wiki/20.109%28F10%29 20.109 Laboratory Fundamentals of Biological Engineering] (core undergraduate course for bioengineering students at 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]
*Teaching Certificate from the [http://tll.mit.edu/ MIT Teaching and Learning Laboratory]
* 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===
===Laboratory tools and resources===
[[Image:BNL_cartoon.jpg|thumb|280px|right|Just another lab door at Brookhaven National Lab]]
*[http://www.qiagen.com/literature/benchguide/bg_pls_lit.aspx Qiagen bench guide]
*[http://www.qiagen.com/literature/benchguide/bg_pls_lit.aspx Qiagen bench guide]


Line 100: Line 127:


*[http://techtv.mit.edu/ MIT Tech TV]
*[http://techtv.mit.edu/ MIT Tech TV]


===Good books===
===Good books===
[[Image:Books_Central_Sq.jpg|thumb|200px|right|Books in Central Square, Cambridge]]
[[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=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

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