Professor Megan O'Mara
Professor

Megan O'Mara

Email: 

Background

Megan O’Mara is a Professor and Group Leader at the Australian Institute for Bioengineering and Nanotechnology (AIBN), UQ. Her group uses multiscale modelling techniques to understand how changes in the biochemical environment of the cell membranes alters membrane properties and modulates the function of membrane proteins. She has research interests in multidrug resistance, computational drug design and delivery, biopolymers, and personalized medicine. Megan completed her PhD in biophysics at the Australian National University in 2005 before moving to the University of Calgary, Canada, to take up a Canadian Institutes of Health Research Postdoctoral Fellowship. In 2009, she returned to Australia to join University of Queensland’s School of Chemistry and Molecular Biosciences as a UQ Postdoctoral Fellow, before commencing an ARC DECRA in 2012 where she continued her computational work on membrane protein dynamics. In 2015, Megan joined the Research School of Chemistry, Australian National University in 2015 as Rita Cornforth Fellow and Senior Lecturer. In 2019 she was promoted to Associate Professor and was Associate Director (Education) of the Research School of Chemistry ANU in 2019-2021. In April 2022 she relocated to AIBN.

Availability

Professor Megan O'Mara is:
Available for supervision
Media expert

Fields of research

Biological Sciences Biological physics Biomedical and Clinical Sciences Biomolecular modelling and design Cell neurochemistry Characterisation of biological macromolecules Chemical Sciences Macromolecular and materials chemistry Medicinal and biomolecular chemistry Molecular medicine Physical Sciences Proteins and peptides Receptors and membrane biology Structural biology (incl. macromolecular modelling) Zoology

Qualifications

  • Bachelor, University of Canberra
  • Bachelor of Physical Sciences, Australian National University
  • Doctor of Philosophy of Physical Sciences, Australian National University
  • Associate Fellow, Australian National University, Australian National University

Research interests

  • computational drug design

    computational drug design, structure based drug design, structure activity relationships, computational fragment based drug design

  • membrane biophysics

    computational cell membrane biophysics, computational lipidomics, cell membrane properties in health, disease and senescence

  • multudrug resistance

    antimicrobial resistance, cancer chemotherapy resistance

  • polymer simulations

    biopolymers, self assembly, polymer properties

  • lipid delivery systems

    targeted lipid delivery systems, computational analysis, lipid formulations, LNP loading, computational simulations

  • computational structural biology

    membrane protein structure-function, computational biology, protein structure prediction

Research impacts

My research uses computational techniques and simulations to understand how the chemistry of biological and bioinspired systems influence their physical properties. My goal is to understand how biomolecules self-assemble and self-regulate in living cells. My work allows the rational design of new pharmaceuticals, drug and vaccine delivery systems and biocompatable materials, as well as understanding fundamental problems such as antibiotic resistance. My students gain skills in data science, computational chemistry, computational biology, high performance computing, rational drug design and research data management that are directly transferable to industry, government and policy development, as well as research. I collaborate broadly across UQ, Australia and internationally with researchers and industry.

Search Professor Megan O'Mara’s works on UQ eSpace

123 works between 2003 and 2024
All (123) Journal Article (100) Book Chapter (4) Conference Publication (19)

61 - 80 of 123 works

2017

Journal Article

Structure of a lipid A phosphoethanolamine transferase suggests how conformational changes govern substrate binding

Anandan, Anandhi, Evans, Genevieve L., Condic-Jurkic, Karmen, O'Mara, Megan L., John, Constance M., Phillips, Nancy J., Jarvis, Gary A., Wills, Siobhan S., Stubbs, Keith A., Moraes, Isabel, Kahler, Charlene M. and Vrielink, Alice (2017). Structure of a lipid A phosphoethanolamine transferase suggests how conformational changes govern substrate binding. Proceedings of the National Academy of Sciences of the United States of America, 114 (9), 2218-2223. doi: 10.1073/pnas.1612927114

Structure of a lipid A phosphoethanolamine transferase suggests how conformational changes govern substrate binding

2017

Journal Article

Location of contact residues in pharmacologically distinct drug binding sites on P-glycoprotein

Mittra, Rituparna, Pavy, Megan, Subramanian, Nanditha, George, Anthony M., O'Mara, Megan L., Kerr, Ian D. and Callaghan, Richard (2017). Location of contact residues in pharmacologically distinct drug binding sites on P-glycoprotein. Biochemical Pharmacology, 123, 19-28. doi: 10.1016/j.bcp.2016.10.002

Location of contact residues in pharmacologically distinct drug binding sites on P-glycoprotein

2017

Book Chapter

Thylakoid ultrastructure: visualizing the photosynthetic machinery

Steinbeck, Janina, O’Mara, Megan L., Ross, Ian L., Stahlberg, Henning and Hankamer, Ben (2017). Thylakoid ultrastructure: visualizing the photosynthetic machinery. Chlamydomonas: Biotechnology and Biomedicine. (pp. 149-191) edited by Michael Hippler. Cham, Switzerland: Springer International Publishing. doi: 10.1007/978-3-319-66360-9_7

Thylakoid ultrastructure: visualizing the photosynthetic machinery

2017

Journal Article

Synthetically controlling dendrimer flexibility improves delivery of large plasmid DNA

Kretzmann, Jessica A., Ho, Diwei, Evans, Cameron W., Plani-Lam, Janice H. C., Garcia-Bloj, Benjamin, Mohamed, A. Elaaf, O'Mara, Megan L., Ford, Ethan, Tan, Dennis E. K., Lister, Ryan, Blancafort, Pilar, Norret, Marck and Iyer, K. Swaminathan (2017). Synthetically controlling dendrimer flexibility improves delivery of large plasmid DNA. Chemical Science, 8 (4), 2923-2930. doi: 10.1039/c7sc00097a

Synthetically controlling dendrimer flexibility improves delivery of large plasmid DNA

2017

Journal Article

Simple design of an enzyme-inspired supported catalyst based on a catalytic triad

Nothling, Mitchell D., Ganesan, Aravindhan, Condic-Jurkic, Karmen, Pressly, Eric, Davalos, Ashley, Gotrik, Michael R., Xiao, Zeyun, Khoshdel, Ezat, Hawker, Craig J., O'Mara, Megan L., Coote, Michelle L. and Connal, Luke A. (2017). Simple design of an enzyme-inspired supported catalyst based on a catalytic triad. Chem, 2 (5), 732-745. doi: 10.1016/j.chempr.2017.04.004

Simple design of an enzyme-inspired supported catalyst based on a catalytic triad

2017

Journal Article

Erratum: Simple Design of an Enzyme-Inspired Supported Catalyst Based on a Catalytic Triad (Chem (2017) 2(5) (732–745) (S2451929417301705) (10.1016/j.chempr.2017.04.004))

Nothling, Mitchell D., Ganesan, Aravindhan, Condic-Jurkic, Karmen, Pressly, Eric, Davalos, Ashley, Gotrik, Michael R., Xiao, Zeyun, Khoshdel, Ezat, Hawker, Craig J., O'Mara, Megan L., Coote, Michelle L. and Connal, Luke A. (2017). Erratum: Simple Design of an Enzyme-Inspired Supported Catalyst Based on a Catalytic Triad (Chem (2017) 2(5) (732–745) (S2451929417301705) (10.1016/j.chempr.2017.04.004)). Chem, 2 (6), 893-894. doi: 10.1016/j.chempr.2017.05.015

Erratum: Simple Design of an Enzyme-Inspired Supported Catalyst Based on a Catalytic Triad (Chem (2017) 2(5) (732–745) (S2451929417301705) (10.1016/j.chempr.2017.04.004))

2016

Journal Article

Rangefinder: a semisynthetic FRET sensor design algorithm

Mitchell, Joshua A., Whitfield, Jason H., Zhang, William H., Henneberger, Christian, Janovjak, Harald, O'Mara, Megan L. and Jackson, Colin J. (2016). Rangefinder: a semisynthetic FRET sensor design algorithm. ACS Sensors, 1 (11), 1286-1290. doi: 10.1021/acssensors.6b00576

Rangefinder: a semisynthetic FRET sensor design algorithm

2016

Journal Article

Hydrophobic shielding drives catalysis of hydride transfer in a family of F420H2-dependent enzymes

Mohamed, A. Elaaf, Condic-Jurkic, Karmen, Ahmed, F. Hafna, Yuan, Peng, O'Mara, Megan L., Jackson, Colin J. and Coote, Michelle L. (2016). Hydrophobic shielding drives catalysis of hydride transfer in a family of F420H2-dependent enzymes. Biochemistry, 55 (49), 6908-6918. doi: 10.1021/acs.biochem.6b00683

Hydrophobic shielding drives catalysis of hydride transfer in a family of F420H2-dependent enzymes

2016

Journal Article

Rv2074 is a novel F420H2-dependent biliverdin reductase in Mycobacterium tuberculosis

Ahmed, F. Hafna, Mohamed, A. Elaaf, Carr, Paul D., Lee, Brendon M., Condic-Jurkic, Karmen, O'Mara, Megan L. and Jackson, Colin J. (2016). Rv2074 is a novel F420H2-dependent biliverdin reductase in Mycobacterium tuberculosis. Protein Science, 25 (9), 1692-1709. doi: 10.1002/pro.2975

Rv2074 is a novel F420H2-dependent biliverdin reductase in Mycobacterium tuberculosis

2016

Journal Article

Correction: Identification of a 3rd Na+ binding site of the glycine transporter, GlyT2

Subramanian, Nandhitha, Scopelliti, Amanda J., Carland, Jane E., Ryan, Renae M., O'Mara, Megan L. and Vandenberg, Robert J. (2016). Correction: Identification of a 3rd Na+ binding site of the glycine transporter, GlyT2. PLoS One, 11 (7) e0159896, e0159896. doi: 10.1371/journal.pone.0159896

Correction: Identification of a 3rd Na+ binding site of the glycine transporter, GlyT2

2016

Journal Article

Identification of a 3rd Na+ binding site of the glycine transporter, GlyT2

Subramanian, Nandhitha, Scopelitti, Amanda J., Carland, Jane E., Ryan, Renae M., O'Mara, Megan L. and Vandenberg, Robert J. (2016). Identification of a 3rd Na+ binding site of the glycine transporter, GlyT2. PLoS ONE, 11 (6) e0157583, e0157583. doi: 10.1371/journal.pone.0157583

Identification of a 3rd Na+ binding site of the glycine transporter, GlyT2

2016

Journal Article

Structural and dynamic perspectives on the promiscuous transport activity of P-glycoprotein

Subramanian, Nandhitha, Condic-Jurkic, Karmen and O'Mara, Megan L. (2016). Structural and dynamic perspectives on the promiscuous transport activity of P-glycoprotein. Neurochemistry International, 98, 146-152. doi: 10.1016/j.neuint.2016.05.005

Structural and dynamic perspectives on the promiscuous transport activity of P-glycoprotein

2016

Journal Article

Understanding the accumulation of P-glycoprotein substrates within cells: The effect of cholesterol on membrane partitioning

Subramanian, Nandhitha, Schumann-Gillett, Alexandra, Mark, Alan E. and O'Mara, Megan L. (2016). Understanding the accumulation of P-glycoprotein substrates within cells: The effect of cholesterol on membrane partitioning. Biochimica et Biophysica Acta: Biomembranes, 1858 (4), 776-782. doi: 10.1016/j.bbamem.2015.12.025

Understanding the accumulation of P-glycoprotein substrates within cells: The effect of cholesterol on membrane partitioning

2016

Conference Publication

Going downstream - how does GH binding activate JAK2

Brooks, Andrew, Dai, W., O'Mara, M. L., Abankwa, D., Chhabra, Y., Pelekanos, R. A., Gardon, O., Tunny, K. A., Blucher, K. M., Morton, C. J., Parker, M. W., Sierecki, E., Gambin, Y., Gomez, G. A., Alexandrov, K., Wilson, I. A., Doxastakis, M., Mark, A. E. and Waters, M. J. (2016). Going downstream - how does GH binding activate JAK2. Annual Scientific Meeting of the Endocrine Society of Australia, Adelaide, Australia, 23-26 August, 2015. Chichester, West Sussex, United Kingdom: Wiley-Blackwell Publishing. doi: 10.1111/cen.13010

Going downstream - how does GH binding activate JAK2

2016

Conference Publication

Mechanism of JAK2 Activation by the Archetype Class I Cytokine Receptor, the Growth Hormone Receptor

Brooks, Andrew J., O’Mara, Megan L., Dai, Wei, Abankwa, Daniel, Chhabra, Yash, Tunny, Kathryn A., Parker, Michael W., Sierecki, Emma, Gambin, Yann, Gomez, Guillermo A., Haxholm, Gitte W., Nikolajsen, Louise F., Doxastakis, Manolis, Mark, Alan E. and Waters, Michael J. (2016). Mechanism of JAK2 Activation by the Archetype Class I Cytokine Receptor, the Growth Hormone Receptor. Biophysical Meeting, Los Angeles, CA, United States, 27 February - 2 March 2016. CAMBRIDGE: CELL PRESS. doi: 10.1016/j.bpj.2015.11.233

Mechanism of JAK2 Activation by the Archetype Class I Cytokine Receptor, the Growth Hormone Receptor

2015

Journal Article

Characterizing the conformational dynamics of metal-free PsaA usingmolecular dynamics simulations and electron paramagnetic resonance spectroscopy

Deplazes, Evelyne, Begg, Stephanie L., van Wonderen, Jessica H., Campbell, Rebecca, Kobe, Bostjan, Paton, James C., MacMillan, Fraser, McDevitt, Christopher A. and O'Mara, Megan L. (2015). Characterizing the conformational dynamics of metal-free PsaA usingmolecular dynamics simulations and electron paramagnetic resonance spectroscopy. Biophysical Chemistry, 207, 51-60. doi: 10.1016/j.bpc.2015.08.004

Characterizing the conformational dynamics of metal-free PsaA usingmolecular dynamics simulations and electron paramagnetic resonance spectroscopy

2015

Journal Article

Molecular basis for the interaction of the mammalian amino acid transporters B0AT1 and B0AT3 with their ancillary protein collectrin

Fairweather, Stephen J., Broeer, Angelika, Subramanian, Nandhitha, Turner, Ennrah, Cheng, Qi, Schmoll, Dieter, O'Mara, Megan L. and Broeer, Stefan (2015). Molecular basis for the interaction of the mammalian amino acid transporters B0AT1 and B0AT3 with their ancillary protein collectrin. Journal of Biological Chemistry, 290 (40), 24308-24325. doi: 10.1074/jbc.M115.648519

Molecular basis for the interaction of the mammalian amino acid transporters B0AT1 and B0AT3 with their ancillary protein collectrin

2015

Journal Article

Identification of possible binding sites for morphine and nicardipine on the multidrug transporter P-Glycoprotein using umbrella sampling techniques

Subramanian, Nandhitha, Condic-Jurkic, Karmen, Mark, Alan E. and O'Mara, Megan L. (2015). Identification of possible binding sites for morphine and nicardipine on the multidrug transporter P-Glycoprotein using umbrella sampling techniques. Journal of Chemical Information and Modeling, 55 (6), 1202-1217. doi: 10.1021/ci5007382

Identification of possible binding sites for morphine and nicardipine on the multidrug transporter P-Glycoprotein using umbrella sampling techniques

2015

Journal Article

Dysregulation of transition metal ion homeostasis is the molecular basis for cadmium toxicity in Streptococcus pneumoniae

Begg, Stephanie L., Eijkelkamp, Bart A., Luo, Zhenyao, Couñago, Rafael M., Morey, Jacqueline R., Maher, Megan J., Ong, Cheryl-lynn Y., McEwan, Alastair G., Kobe, Bostjan, O'Mara, Megan L., Paton, James C. and McDevitt, Christopher A. (2015). Dysregulation of transition metal ion homeostasis is the molecular basis for cadmium toxicity in Streptococcus pneumoniae. Nature Communications, 6 (6418) 6418, 1-11. doi: 10.1038/ncomms7418

Dysregulation of transition metal ion homeostasis is the molecular basis for cadmium toxicity in Streptococcus pneumoniae

2015

Conference Publication

Insights into the operations of a promiscuous drug trafficker: The story of P-glycoprotein

Condic-Jurkic, K., Subramanian, N., Mark, A. E. and O'Mara, M. (2015). Insights into the operations of a promiscuous drug trafficker: The story of P-glycoprotein. 10th European Biophysical Societies Association (EBSA) European Biophysics Congress, Dresden, Germany, 18-22 July 2015. Heidelberg, Germany: Springer. doi: 10.1007/s00249-015-1045-6

Insights into the operations of a promiscuous drug trafficker: The story of P-glycoprotein

Current funding

  • 2025 - 2027
    Quantum-Enabled Low-Field Magnetic Resonance Imaging for High-Performance Sport
    Queensland Government Department of Environment, Science and Innovation
    Open grant
  • 2023 - 2026
    Overcoming antiseptic and disinfectant resistance in staphylococci (NHMRC Ideas Grant administered by Flinders University)
    Flinders University
    Open grant

Past funding

  • 2022 - 2024
    Synthetic Biology for Synthesis of Novel Polymers Used in Energy Storage
    Commonwealth Defence Science and Technology Group
    Open grant
  • 2015
    Characterising new therapeutic targets in the fight against pneumococcal disease using computational simulations as an alternative to animal models
    The MAWA Trust
    Open grant
  • 2014
    A parallel computer facility for modelling and simulation
    UQ Major Equipment and Infrastructure
    Open grant
  • 2013 - 2015
    Membrane proteins: Understanding biological switches, motors and triggers.
    ARC Discovery Projects
    Open grant
  • 2013 - 2016
    Understanding multidrug resistance in cancer: identification of the substrate and inhibitor binding sites in P-glycoprotein
    NHMRC Project Grant
    Open grant
  • 2012
    ResTeach Funding 2012 0.05 FTE School of Math & Physics
    UQ ResTeach
    Open grant
  • 2012 - 2015
    Understanding multidrug resistance: identifying the molecular basis of substrate and inhibitor transport by P-glycoprotein
    ARC Discovery Early Career Researcher Award
    Open grant
  • 2012
    ResTeach Funding 2012 0.05 FTE School of Chemistry and Molecular Biosciences
    UQ ResTeach
    Open grant
  • 2010 - 2011
    ResTeach 2010 0.1 FTE School of Chemistry and Molecular Biosciences
    UQ ResTeach
    Open grant
  • 2010
    The mechanism of viral entry into cells: understanding how Glycoprotein 2 from Ebola initiates membrane fusion
    UQ Early Career Researcher
    Open grant
  • 2010 - 2012
    The role of glutamine transporter SNAT3 in ion transport, cell signalling and ammonia detoxification (NHMRC project grant administered by the Australian National University)
    Australian National University
    Open grant

Availability

Professor Megan O'Mara is:
Available for supervision

Before you email them, read our advice on how to contact a supervisor.

Available projects

  • Computational design of biocompatable delivery systems

    Biocompatible delivery systems allow enhanced delivery of pharmaceuticals, vaccines and other biological payload molecules, with varied effects including extending the pharmaceutical half-life of drugs, increasing adsorption and decreasing immunogenicity. While these agents have increased the efficacy of many biological therapies, very little work has been done on improving the targeting of these agents to the specific cell or receptor of interest. This project will examine strategies to increase the selectivity of biopolymer delivery systems to enhance the ability to target specific cell types or receptors, thereby reducing off target effects. This project will identify the chemical composition and biophysical characteristics of different cell membranes, and how this impacts their interaction with biopolymer delivery systems. The project requires good collaboration skills, an broad understanding of chemistry and biochemistry, and strong skills in multiscale modelling techniques, from QMMM to coarse grained molecular dynamics.

  • The impact of lipid modifications on cell membrane function

    Membrane lipid composition influences the localisation of membrane proteins and regulates their activity. The hundreds of chemically distinct lipids within cell membranes phase-separate to form microdomains that impact the localisation and interactions of membrane proteins. The composition of the cell membrane is tightly controlled in normal cellular function. There is now considerable evidence that altered cell homeostasis, ranging from inflammatory processes to cancer, cause alterations in metabolic pathways which impact membrane lipid distributions, cell biophysical properties and membrane protein function. This may have downstream impacts on the uptake and efficacy of a range of pharmaceuticals used to treat dysfunction. Using data derived from mass spectrometry and other experimental approaches, this project will use multiscale simulation techniques to examine how changes in lipid membrane composition in cancer and other disease states impacts drug uptake. This knowledge will provide a means to specifically target a given cell type through the drug delivery systems and targeted therapeutics.

  • Membrane mediated antimicrobial resistance

    Bacterial multidrug efflux pumps are the bacteria’s first line of defence against the action of antimicrobials. However, very little is currently known about the function and substrate range of these efflux pumps. This project will examine different multidrug efflux pumps to uncover the structural basis of substrate specificity and transport. It will examine the impact of bacterial membrane modifications on bacterial multidrug efflux pump function, and how peptide- and/or polymer-based antimicrobials inhibit multidrug efflux pumps and disrupt membrane integrity. Other avenues of investigation include characterising the effect of lipid modifications in antimicrobial resistance, and computational drug design of lead new candidates for antimicrobial design. This project uses a range of computational techniques, primarily multiscale molecular dynamics simulations.

  • Allosteric modulation of synaptic transmission by neurosteroids and oxysterols

    The development of effective therapeutics that target chronic pain in neurological diseases would significantly improve the quality of life for millions of people living with chronic pain. The glycinergic neuronal transport proteins are a promising target for the treatment of chronic pain. In neurons and other cells, the membrane lipid composition influences the localisation of membrane proteins and regulates their activity. The hundreds of chemically distinct lipids within cell membranes phase-separate to form microdomains that impact the localisation and interactions of membrane proteins. Oxidative stress is an early hallmark of inflammation and disease that causes chemical modifications to membrane lipids, proteins, and other biomolecules. This impacts their function and influences their biophysical properties. This project will examine the effect of oxysterols and neurosteroids on the inhibition of glycernergic synaptic membrane proteins for the development of targeted therapeutics for the treatment of chronic pain in specific disease states. This is a computational project. The direction of the project can be tailored to the interests of the student.

Supervision history

Current supervision

  • Doctor Philosophy

    Unravelling the Physicochemical Drivers of Biomolecular Self-Assembly though Multiscale Simulations

    Principal Advisor

    Other advisors: Professor David Ascher, Dr Evelyne Deplazes

  • Doctor Philosophy

    Computational design of targeted lipid technologies

    Principal Advisor

    Other advisors: Professor David Ascher

  • Doctor Philosophy

    Targeting alterations in cell membrane biophysics for disease intervention

    Principal Advisor

    Other advisors: Dr Evelyne Deplazes

  • Doctor Philosophy

    The effect of membrane composition on protein-ligand interactions in drug design and delivery

    Principal Advisor

    Other advisors: Professor Debra Bernhardt

  • Doctor Philosophy

    Investigation of the mechanisms of antimicrobial resistance and design of novel antimicrobials

    Principal Advisor

    Other advisors: Dr Evelyne Deplazes

Completed supervision

Enquiries

Contact Professor Megan O'Mara directly for media enquiries about:

  • biophysics
  • computational chemistry
  • drug design
  • supercomputers - applications
  • women in STEM

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