
Overview
Background
Associate Professor Muttenthaler is a medicinal chemist working at the interface of chemistry and biology with a strong passion for translational research. His research focuses on bioactive peptides and exploring Nature's biodiversity to develop advanced molecular tools, diagnostics, and therapeutics. His background in drug discovery and development, as well as his interdisciplinary training in the fields of chemistry, molecular biology and pharmacology, assist him in characterising these often highly potent and selective compounds to study their interactions with human physiology for medical innovations in pain, cancer, gut disorders and neurological diseases.
Availability
- Associate Professor Markus Muttenthaler is:
- Available for supervision
- Media expert
Fields of research
Qualifications
- Bachelor of Science, Technische Universität Wien
- Masters (Coursework) of Science, Technische Universität Wien
- Doctor of Philosophy, The University of Queensland
Research interests
-
Neuropeptide Chemistry and Biology
-
Biological and Medicinal Chemistry
-
Peptide Drug Discovery and Development
-
Oxytocin and Vasopressin Research
-
Venom Peptide Drug Discovery
-
Gastrointestinal Disorders
-
Molecular Probe Development
-
Intranasal Peptide Delivery
-
Peptide Chemistry
-
Gastrointestinal wound healing
-
Breast Cancer
-
Multivalent Peptide Dendrimers
-
Selenochemistry
Research impacts
Peptides are key mediators in many biological functions and understanding of their interaction with target proteins is fundamental to unravel the underlying mechanism of diseases. Over the years, an increasing number of bioactive peptides from animals, plants, and bacteria have been characterised, with the overwhelming realisation that these molecules often show better therapeutic performance than their human counterparts, particularly in terms of in vivo stability. The main research efforts situated in this field of Chemical Biology focus on the exploration and translation of these vast and untapped natural libraries towards the development of useful research tools and therapeutics. Solid-phase peptide synthesis, the main tool to access these compounds, is a powerful technology for the assembly and chemical modification of these highly chiral and structurally complex peptides. This complexity is also responsible for their remarkable selectivity and potency as well as for their low side effect profile observed in the clinic.
Works
Search Professor Markus Muttenthaler’s works on UQ eSpace
2013
Journal Article
Evaluation of diverse peptidyl motifs for cellular delivery of semiconductor quantum dots Optical Nanosensing in Cells
Gemmill, Kelly Boeneman, Muttenthaler, Markus, Delehanty, James B., Stewart, Michael H., Susumu, Kimihiro, Dawson, Philip E. and Medintz, Igor L. (2013). Evaluation of diverse peptidyl motifs for cellular delivery of semiconductor quantum dots Optical Nanosensing in Cells. Analytical and Bioanalytical Chemistry, 405 (19), 6145-6154. doi: 10.1007/s00216-013-6982-2
2013
Conference Publication
Insights into the molecular evolution of oxytocin receptor ligand binding
Koehbach, Johannes, Stockner, Thomas, Bergmayr, Christian, Muttenthaler, Markus and Gruber, Christian W. (2013). Insights into the molecular evolution of oxytocin receptor ligand binding. London, United Kingdom: Portland Press. doi: 10.1042/BST20120256
2013
Conference Publication
Peptide-mediated cellular delivery of semiconductor quantum dots
Gemmill, K.B., Muttenthaler, M., Delehanty, J., Deschamps, J., Susumu, K., Stewart, M., Dawson, P., Huston, A. and Medintz, I. (2013). Peptide-mediated cellular delivery of semiconductor quantum dots. Conference on Sensing Technologies for Global Health, Military Medicine, and Environmental Monitoring III, Baltimore, United States, Apr 29-May 01, 2013. Bellingham, WA, United States: S P I E - International Society for Optical Engineering. doi: 10.1117/12.2015446
2012
Journal Article
Exploring bioactive peptides from natural sources for oxytocin and vasopressin drug discovery
Gruber, Christian W., Koehbach, Johannes and Muttenthaler, Markus (2012). Exploring bioactive peptides from natural sources for oxytocin and vasopressin drug discovery. Future Medicinal Chemistry, 4 (14), 1791-1798. doi: 10.4155/FMC.12.108
2012
Journal Article
Abundance and diversity of Conus species (Gastropoda: Conidae) at the northern tip of New Ireland province of Papua New Guinea
Muttenthaler, Markus, Dutertre, Sebastien, Wingerd, Joshua S., Aini, John W., Walton, Hugh, Alewood, Paul F. and Lewis, Richard J. (2012). Abundance and diversity of Conus species (Gastropoda: Conidae) at the northern tip of New Ireland province of Papua New Guinea. Nautilus, 126 (2), 47-56.
2012
Journal Article
Discovery of defense- and neuropeptides in social ants by genome-mining
Gruber, Christian W. and Muttenthaler, Markus (2012). Discovery of defense- and neuropeptides in social ants by genome-mining. PloS One, 7 (3) e32559, e32559. doi: 10.1371/journal.pone.0032559
2012
Conference Publication
Novel sources for potent and selective GPCR modulators
Muttenthaler, M., Dawson, P. E., Gruber, C. W., Bergmayr, C., Freissmuth, M., Andersson, A., Vetter, I., Dutertre, S., Lewis, R. J. and Alewood, P. F. (2012). Novel sources for potent and selective GPCR modulators. 32nd European Peptide Symposium, Athens, Greece, 2-7 September 2012. Chichester, West Sussex United Kingdom: John Wiley & Sons. doi: 10.1002/psc.2447
2012
Conference Publication
Pharmacological characterization of circular plant peptides with oxytocin-like activity
Koehbach, J., O'Brien, M., Miazzo, M., Muttenthaler, M., Akcan, M., Smith, T. J., Craik, D. J., Freissmuth, M. and Gruber, C. W. (2012). Pharmacological characterization of circular plant peptides with oxytocin-like activity. 32nd European Peptide Symposium "Peptides 2012", Athens, Greece, 02-07 September 2012. West Sussex, United Kingdom: John Wiley and Sons. doi: 10.1002/psc.2449
2012
Conference Publication
Pharmacological applications of natural peptide libraries
Koehbach, Johannes, Muttenthaler, Markus, Gründemann, Carsten and Gruber, Christian W (2012). Pharmacological applications of natural peptide libraries. 18th Scientific Symposium of the Austrian Pharmacological Society (APHAR), Graz, Austria, 20-21 September, 2012. London, United Kingdom: Springer Nature. doi: 10.1186/2050-6511-13-s1-a31
2011
Journal Article
Site-specific pKa determination of selenocysteine residues in selenovasopressin using 77Se NMR
Mobli, Mehdi, Morgenstern, David, King, Glenn F., Alewood, Paul F. and Muttenthaler, Markus (2011). Site-specific pKa determination of selenocysteine residues in selenovasopressin using 77Se NMR. Angewandte Chemie (International Edition), 50 (50), 11952-11955. doi: 10.1002/anie.201104169
2011
Journal Article
Structure-activity studies on alpha-conotoxins
Muttenthaler, Markus, Akondi, Kalyana B. and Alewood, Paul F. (2011). Structure-activity studies on alpha-conotoxins. Current Pharmaceutical Design, 17 (38), 4226-4241. doi: 10.2174/138161211798999384
2011
Conference Publication
Conotoxins - blueprints for GPCR drug discovery?
Muttenthaler, M., Gruber, C. W., Andersson, A., Vetter, I., Nevin, S. T., Grishin, A. A., Dutertre, S., Daly, N. L., Craik, D. J., Adams, D. J., Lewis, R. J. and Alewood, P. F. (2011). Conotoxins - blueprints for GPCR drug discovery?. 22nd American Peptide Symposium, San Diego, CA, United States, 25-30 June 2011. Hoboken, NJ, United States: John Wiley & Sons.
2010
Journal Article
Modulating oxytocin activity and plasma stability by disulfide bond engineering
Muttenthaler, Markus, Andersson, Asa, Dantas de Araujo, Aline, Dekan, Zoltan, Lewis, Richard J. and Alewood, Paul F. (2010). Modulating oxytocin activity and plasma stability by disulfide bond engineering. Journal of Medicinal Chemistry, 53 (24), 8585-8596. doi: 10.1021/jm100989w
2010
Journal Article
Ligand-based peptide design and combinatorial peptide libraries to target G protein-coupled receptors
Gruber, Christian W., Muttenthaler, Markus and Freissmuth, Michael (2010). Ligand-based peptide design and combinatorial peptide libraries to target G protein-coupled receptors. Current Pharmaceutical Design, 16 (28), 3071-3088. doi: 10.2174/138161210793292474
2010
Journal Article
α-Conotoxin AuIB isomers exhibit distinct inhibitory mechanisms and differential sensitivity to stoichiometry of α3β4 nicotinic acetylcholine receptors
Grishin, Anton, Wang, Ching-I. A., Muttenthaler, Markus, Alewood, Paul F., Lewis, Richard J. and Adams, David J. (2010). α-Conotoxin AuIB isomers exhibit distinct inhibitory mechanisms and differential sensitivity to stoichiometry of α3β4 nicotinic acetylcholine receptors. Journal of Biological Chemistry, 285 (29), 22254-22263. doi: 10.1074/jbc.M110.111880
2010
Journal Article
Solving the alpha-conotoxin folding problem: Efficient selenium-directed on-resin generation of more potent and stable nicotinic acetylcholine receptor antaqonists
Muttenthaler, Marcus, Nevin, Simon T., Grishin, Anton A., Ngo, Shyuan T., Choy, Peng T., Daly, Norelle L., Hu, Shu-Hong, Armishaw, Christopher J., Wang, Ching-I. A., Lewis, Richard J., Martin, Jennifer L., Noakes, Peter G., Craik, David J., Adams, David J. and Alewood, Paul F. (2010). Solving the alpha-conotoxin folding problem: Efficient selenium-directed on-resin generation of more potent and stable nicotinic acetylcholine receptor antaqonists. Journal of the American Chemical Society, 132 (10), 3514-3522. doi: 10.1021/ja910602h
2010
Conference Publication
Oxytocin agonist design - A selenocysteine mimetic reveals a functional selectivity switch for the human oxytocin receptor
Muttenthaler, M. M., de Araujo, A. D., Andersson, A., Vetter, I., Gruber, C., Ramos, Y. Garcia, Feytens, D., Bergmayr, C., Freissmuth, M., Lewis, R. and Alewood, P. (2010). Oxytocin agonist design - A selenocysteine mimetic reveals a functional selectivity switch for the human oxytocin receptor. 31st European Peptide Symposium, Copenhagen, Denmark, 5-9 September 2010. Chichester, West Sussex, U.K.: John Wiley & Sons. doi: 10.1002/psc.1303
2010
Journal Article
p-Nitrobenzyl protection for cysteine and selenocysteine: A more stable alternative to the acetamidomethyl group
Muttenthaler, Markus, Ramos, Yesica Garcia, Feytens, Debby, Dantas de Araujo, Aline and Alewood, Paul F. (2010). p-Nitrobenzyl protection for cysteine and selenocysteine: A more stable alternative to the acetamidomethyl group. Biopolymers, 94 (4), 423-432. doi: 10.1002/bip.21502
2009
Other Outputs
Peptide engineering - controlling the folding of disulfide-rich peptides
Muttenthaler, Markus (2009). Peptide engineering - controlling the folding of disulfide-rich peptides. PhD Thesis, Institute for Molecular Bioscience, The University of Queensland.
2009
Book Chapter
Selenocystine peptides - synthesis, folding and applications
Muttenthaler, M. and Alewood, P. F. (2009). Selenocystine peptides - synthesis, folding and applications. Oxidative folding of peptides and proteins. (pp. 396-418) edited by Johannes Buchner. Cambridge , U.K.: Royal Society of Chemistry. doi: 10.1039/9781847559265-00396
Funding
Current funding
Supervision
Availability
- Associate Professor Markus Muttenthaler is:
- Available for supervision
Before you email them, read our advice on how to contact a supervisor.
Available projects
-
Oxytocin and Vasopressin Research
Please contact Dr Muttenthaler directly for further details
-
Venom peptide drug discovery
Please contact Dr Muttenthaler directly for further details.
-
Breast Cancer
Please contact Dr Muttenthaler directly for further details.
-
Ligand design and chemical synthesis
Project for interns or summer student.
Please contact Dr Muttenthaler directly for further details.
-
Gastrointestinal wound healing
Please contact Dr Muttenthaler directly for further details.
Supervision history
Current supervision
-
Doctor Philosophy
Medicinal chemistry strategies to remove bacterial biofilms associated with gastrointestinal disorders
Principal Advisor
Other advisors: Professor Mark Blaskovich
-
Doctor Philosophy
Targeting bacterial biofilms in patients with gastrointestinal disorders
Principal Advisor
Other advisors: Professor Mark Blaskovich
-
Doctor Philosophy
Venom-derived peptides to study heart function and treat cardiovasculardisease
Principal Advisor
Other advisors: Professor Nathan Palpant
-
Doctor Philosophy
Discovery and development of highly stable venom-derived peptide drug leads.
Principal Advisor
Other advisors: Associate Professor Johan Rosengren
-
Doctor Philosophy
Molecular probes to study the role of OTR in health and disease
Principal Advisor
-
Doctor Philosophy
Development of venom-derived blood-brain barrier shuttles
Principal Advisor
Other advisors: Associate Professor Johan Rosengren
Completed supervision
-
2023
Doctor Philosophy
Venom Components as Analgesics and Pharmacological Tools to Elucidate Mammalian Pain Signalling Pathways
Associate Advisor
Other advisors: Dr Fernanda Cardoso, Professor Glenn King
-
2021
Doctor Philosophy
Novel mechanistic insights into oxytocin receptor signalling in breast cancer
Associate Advisor
Other advisors: Professor David Fairlie
-
2021
Doctor Philosophy
Targeting the oxytocin receptor for breast cancer imaging
Associate Advisor
Other advisors: Professor David Fairlie
-
2020
Doctor Philosophy
Trefoil factor family: chemical synthesis, mechanisms of action and therapeutic potential for gastrointestinal disorders
Associate Advisor
-
2020
Doctor Philosophy
Mining for neuropeptides: A bioinformatic and biochemical approach to characterise neuropeptides in animal venoms
Associate Advisor
Other advisors: Professor David Craik
-
2020
Doctor Philosophy
Detecting Oxytocin: Mass spectrometry and PET-tracer development
Associate Advisor
Other advisors: Professor David Fairlie
-
2019
Doctor Philosophy
Investigation of the venom of the Estuarine Stonefish, Synanceia horrida
Associate Advisor
Media
Enquiries
Contact Associate Professor Markus Muttenthaler directly for media enquiries about:
- bioactive peptides
- chemical biology
- cone snails
- conotoxins
- drug discovery and development
- medicinal chemistry
- neuropeptides
- oxytocin
- peptide and protein synthesis
- vasopressin
- venoms
Need help?
For help with finding experts, story ideas and media enquiries, contact our Media team: