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Dr Fernanda Cardoso
Dr

Fernanda Cardoso

Email: 
Phone: 
+61 7 344 33402

Overview

Background

Dr Fernanda Cardoso is a Brazil-born Australian researcher interested in venom peptide-based biodiscovery and therapeutics development. Cardoso was awarded an MSc in Molecular Pharmacology and a PhD with an emphasis in Biochemistry and Immunology and is part of the Institute for Molecular Bioscience, where she develops novel therapies for complex neurological diseases. Cardoso has interdisciplinary training in the fields of neuropharmacology, medicinal chemistry and chemical biology and a strong background in drug discovery, which provides the skills to identify naturally occurring or synthetic bioactive molecules and to study their effects in human physiology with applications in neurologic disorders such as chronic pain, irritable bowel syndrome (IBS), and motor neuron disease (MND). Please see Dr Cardoso’s Grants and Publications list for more details.

Before joining the University of Queensland, Dr Cardoso was part of the Queensland Institute for Medical Research, holding a prestigious CAPES Postdoctoral Fellowship. During this period, Cardoso developed unique high-throughput screen platforms for discovering protein and peptide targets of novel therapies to combat infectious diseases and novel helminth-derived bioactives with anti-inflammatory properties. Please see Dr Cardoso’s Publications list for more details.

Dr Cardoso is currently part of the Centre for Drug Discovery and manages several industry and academic projects studying ion channel modulators derived from natural repertoires, particularly venoms, and developing novel, effective drugs to treat neurological disorders.

Availability

Dr Fernanda Cardoso is:
Available for supervision
Media expert

Qualifications

  • Bachelor, Universidade Federal de Minas Gerais (UFMG)
  • Masters (Research) of Biological Sciences, Universidade Federal de Minas Gerais (UFMG)
  • Doctor of Philosophy, Universidade Federal de Minas Gerais (UFMG)

Research interests

  • Chronic pain - Mechanisms of pain and Therapeutics development, Visceral Pain, Irritable Bowel Syndrome

  • Neurodegeneration - Pathophysiology and Therapeutics development

  • Venomics and Pharmacology of Spiders, Cone snails and Snake venoms

  • Structure-function properties of venom peptides and proteins

  • Voltage-gated Ion Channels

Research impacts

Dr. Fernanda Cardoso's research has provided remarkable insights into the discovery and biology of new agents for therapeutical use in complex disorders such as chronic pain, irritable bowel syndrome and motor neuron disease, and vaccinology against tropical diseases. Her ongoing research in ion channel modulators has provided unique leads for treating neuropathic pain and neurodegenerative disorders, which could improve the lives of millions of individuals around the globe, and her past discoveries in vaccine research have the potential to improve the lives of millions of people in Africa, Asia and South America through a vaccine against schistosomiasis.

Works

Search Professor Fernanda Cardoso’s works on UQ eSpace

124 works between 2003 and 2024

81 - 100 of 124 works

2017

Journal Article

The structure, dynamics and selectivity profile of a NaV 1.7 potency-optimised huwentoxin-IV variant

Rahnama, Sassan, Deuis, Jennifer R., Cardoso, Fernanda C., Ramanujam, Venkatraman, Lewis, Richard J., Rash, Lachlan D., King, Glenn F., Vetter, Irina and Mobli, Mehdi (2017). The structure, dynamics and selectivity profile of a NaV 1.7 potency-optimised huwentoxin-IV variant. PLoS One, 12 (3) e0173551, e0173551. doi: 10.1371/journal.pone.0173551

The structure, dynamics and selectivity profile of a NaV 1.7 potency-optimised huwentoxin-IV variant

2017

Conference Publication

Discovery of novel CaV and NaV modulators in spider venoms and applications in the development of drugs to treat chronic pain.

Cardoso, Fernanda C., King, Glenn F. and Lewis, Richard J. (2017). Discovery of novel CaV and NaV modulators in spider venoms and applications in the development of drugs to treat chronic pain.. 19th World Congress of the International Society on Toxinology, Haikou City, Hainan Province, China, 24-31 October 2017.

Discovery of novel CaV and NaV modulators in spider venoms and applications in the development of drugs to treat chronic pain.

2017

Conference Publication

Defining ω-conotoxin binding site and delineating the role of the α2δ1 subunit in ω-conotoxin binding

Hassan, Mahadhi, Abraham, Nikita, Ragnarsson, Lotten K.N., Cardoso, Fernanda C. and Lewis, Richard J. (2017). Defining ω-conotoxin binding site and delineating the role of the α2δ1 subunit in ω-conotoxin binding. Venom to Drugs Conference 2017, Noosa Heads, QLD Australia, 9-14 October 2017.

Defining ω-conotoxin binding site and delineating the role of the α2δ1 subunit in ω-conotoxin binding

2017

Conference Publication

Nav modulators in spider venoms and applications in the development of novel therapies for neurological disorders

Cardoso, Fernanda C., Bellingham, Mark C., King, Glenn F. and Lewis, Richard J. (2017). Nav modulators in spider venoms and applications in the development of novel therapies for neurological disorders. Venom to Drugs Conference 2017, Noosa Heads, QLD Australia, 9-14 October 2017.

Nav modulators in spider venoms and applications in the development of novel therapies for neurological disorders

2017

Conference Publication

High-throughput cell-based assays for screening Cav3.2 modulators from venoms

Wang, D., Herzig, V., Dekan, Z., Ragnarsson, Lotten K. N., Cardoso, Fernanda C. and Lewis, Richard J. (2017). High-throughput cell-based assays for screening Cav3.2 modulators from venoms. Venom to Drugs Conference 2017, Noosa Heads, QLD, Australia, 9-14 October 2017.

High-throughput cell-based assays for screening Cav3.2 modulators from venoms

2016

Journal Article

Isolation and characterization of a structurally unique β-hairpin venom peptide from the predatory ant Anochetus emarginatus

Touchard, Axel, Brust, Andreas, Cardoso, Fernanda C., Chin, K.-Y., Herzig, Volker, Jin, Ai-Hua, Dejean, Alain, Alewood, Paul F., King, Glenn F., Orivel, Jérôme and Escoubas, Pierre (2016). Isolation and characterization of a structurally unique β-hairpin venom peptide from the predatory ant Anochetus emarginatus. Biochimica et Biophysica Acta, 1860 (11 Part A), 2553-2562. doi: 10.1016/j.bbagen.2016.07.027

Isolation and characterization of a structurally unique β-hairpin venom peptide from the predatory ant Anochetus emarginatus

2016

Conference Publication

The inhibition of neuronal calcium channels with aminobenzothiazole derivatives

Sairaman, Anjali, Cardoso, Fernanda Caldas , Lewis, Richard J., Kaliappana, Krishna P., Tuck, Kellie L. and Duggan, Peter J. (2016). The inhibition of neuronal calcium channels with aminobenzothiazole derivatives. RACI Medicinal Chemistry and Chemical Biology Conference 2016, Coogee Beach, NSW, Australia, 7-9 November 2016.

The inhibition of neuronal calcium channels with aminobenzothiazole derivatives

2015

Journal Article

The role of defensive ecological interactions in the evolution of conotoxins

Prashanth, J. R., Dutertre, S., Jin, A. H., Lavergne, V., Hamilton, B., Cardoso, F. C., Griffin, J., Venter, D. J., Alewood, P. F. and Lewis, R. J. (2015). The role of defensive ecological interactions in the evolution of conotoxins. Molecular Ecology, 25 (2), 598-615. doi: 10.1111/mec.13504

The role of defensive ecological interactions in the evolution of conotoxins

2015

Journal Article

Identification and characterization of ProTx-III [μ-TRTX-Tp1a], a new voltage-gated sodium channel inhibitor from venom of the tarantula Thrixopelma pruriens

Cardoso, Fernanda C., Deka, Zoltan, Rosengren, K. Johan, Erickson, Andelain, Vetter, Irina, Deuis, Jennifer R., Herzig, Volker, Alewood, Paul F., King, Glenn F. and Lewis, Richard J. (2015). Identification and characterization of ProTx-III [μ-TRTX-Tp1a], a new voltage-gated sodium channel inhibitor from venom of the tarantula Thrixopelma pruriens. Molecular Pharmacology, 88 (2), 291-303. doi: 10.1124/mol.115.098178

Identification and characterization of ProTx-III [μ-TRTX-Tp1a], a new voltage-gated sodium channel inhibitor from venom of the tarantula Thrixopelma pruriens

2015

Conference Publication

Rational development of novel analgesics for the treatment of chronic pain: Structure-Function studies of an engineered Nav1.7 blocker

Rahnama, S., Lachlan, R., Cardoso, F. C., Smith, J., Deuis, J., Vetter, I., King, G. F. and Mobli, M. (2015). Rational development of novel analgesics for the treatment of chronic pain: Structure-Function studies of an engineered Nav1.7 blocker. The 40th Lorne Conference on Protein Structure and Function, Lorne VIC, Australia, 8-12 February 2015.

Rational development of novel analgesics for the treatment of chronic pain: Structure-Function studies of an engineered Nav1.7 blocker

2015

Conference Publication

Harnessing animal venoms in the discovery of potent Nav inhibitors through fluorescent and automated patch clamp assays

Cardoso, Fernanda Caldas , Herzig, Volker , King, Glenn F. and Lewis, Richard J. (2015). Harnessing animal venoms in the discovery of potent Nav inhibitors through fluorescent and automated patch clamp assays. 18th World Congress of the International Society on Toxinology, Oxford UK, 25-30 September 2015.

Harnessing animal venoms in the discovery of potent Nav inhibitors through fluorescent and automated patch clamp assays

2015

Journal Article

Antibody signatures reflect different disease pathologies in schistosomiasis japonica

Driguez, Patrick, Li, Yuesheng, Gaze, Soraya, Pearson, Mark S., Nakajima, Rie, Trieu, Angela, Doolan, Denise L., Felgner, Philip L., Hou, Xunya, Cardoso, Fernanda C., Jasinskas, Algis, Gobert, Geoffrey, Loukas, Alexander C. and McManus, Donald P. (2015). Antibody signatures reflect different disease pathologies in schistosomiasis japonica. Journal of Infectious Diseases, 213 (1), 122-130. doi: 10.1093/infdis/jiv356

Antibody signatures reflect different disease pathologies in schistosomiasis japonica

2015

Journal Article

Specific humoral response of hosts with variable schistosomiasis susceptibility

Driguez, Patrick, McWilliam, Hamish E. G., Gaze, Soraya, Piedrafita, David, Pearson, Mark S., Nakajima, Rie, Duke, Mary, Trieu, Angela, Doolan, Denise L., Cardoso, Fernanda C., Jasinskas, Algis, Gobert, Geoffrey N., Felgner, Philip L., Loukas, Alex, Meeusen, Els and McManus, Donald P. (2015). Specific humoral response of hosts with variable schistosomiasis susceptibility. Immunology and Cell Biology, 94 (1), 52-65. doi: 10.1038/icb.2015.61

Specific humoral response of hosts with variable schistosomiasis susceptibility

2015

Book Chapter

Does nature do ion channel drug discovery better than us?

Lewis, Richard J., Vetter, Irina, Cardoso, Fernanda C., Inserra, Marco and King, Glenn (2015). Does nature do ion channel drug discovery better than us?. Ion channel drug discovery. (pp. 297-313) edited by Brian Cox and Martin Gosling. Cambridge, United Kingdom: Royal Society of Chemistry. doi: 10.1039/9781849735087-00297

Does nature do ion channel drug discovery better than us?

2014

Journal Article

A multivalent chimeric vaccine composed of Schistosoma mansoni SmTSP-2 and Sm29 was able to induce protection against infection in mice

Pinheiro, Carina S., Ribeiro, Ana Paula Dias, Cardoso, Fernanda C., Martins, Vicente P., Figueiredo, Barbara C. P., Assis, Natan R. G., Morais, Suellen B., Caliari, Marcelo V., Loukas, Alex and Oliveira, Sergio C. (2014). A multivalent chimeric vaccine composed of Schistosoma mansoni SmTSP-2 and Sm29 was able to induce protection against infection in mice. Parasite Immunology, Accepted Article (7), 1-23. doi: 10.1111/pim.12118

A multivalent chimeric vaccine composed of Schistosoma mansoni SmTSP-2 and Sm29 was able to induce protection against infection in mice

2014

Journal Article

An immunomics approach to schistosome antigen discovery: antibody signatures of naturally resistant and chronically infected individuals from endemic areas

Gaze, Soraya, Driguez, Patrick, Pearson, Mark S., Mendes, Tiago, Doolan, Denise L., Trieu, Angela, McManus, Donald P., Gobert, Geoffrey N., Periago, Maria Victoria, Correa Oliveira, Rodrigo, Cardoso, Fernanda C., Oliveira, Guilherme, Nakajima, Rie, Jasinskas, Al, Hung, Chris, Liang, Li, Pablo, Jozelyn, Bethony, Jeffrey M., Felgner, Philip L. and Loukas, Alex (2014). An immunomics approach to schistosome antigen discovery: antibody signatures of naturally resistant and chronically infected individuals from endemic areas. PLoS Pathogens, 10 (3) e1004033, e1004033.1-e1004033.16. doi: 10.1371/journal.ppat.1004033

An immunomics approach to schistosome antigen discovery: antibody signatures of naturally resistant and chronically infected individuals from endemic areas

2014

Conference Publication

Discovery of voltage-gated sodium channel inhibitors from tarantula venoms

Cardoso, F. C., Dekan, Z., Anangi, R., Rosengren, K. J., Erickson, A., Vetter, I., Herzig, V., Alewood, P., King, G. F. and Lewis, R. J. (2014). Discovery of voltage-gated sodium channel inhibitors from tarantula venoms. Venom to Drugs Conference 2014, Kingscliffe, NSW, Australia, 19-23 October 2014.

Discovery of voltage-gated sodium channel inhibitors from tarantula venoms

2014

Conference Publication

Optimizing the potency and selectivity of a spider-venom peptide that inhibitis the analgesic target Nav1.7.

Erickson, A., Cardoso, F. C., Lewis, R. J. and King, G. F. (2014). Optimizing the potency and selectivity of a spider-venom peptide that inhibitis the analgesic target Nav1.7.. Venom to Drugs Conference 2014, Kingscliffe, NSW, Australia, 19-23 October 2014.

Optimizing the potency and selectivity of a spider-venom peptide that inhibitis the analgesic target Nav1.7.

2014

Conference Publication

Unique evolution of D-conotoxins for defence

Prashanth, J. R., Dutertre, S., Jean, A., Lavergne, V., Hamilton, B., Cardoso, F. C., Griffin, J., Venter, D. J., Alewood, P. F. and Lewis, R. J. (2014). Unique evolution of D-conotoxins for defence. Venom to Drugs Conference 2014, Kingscliffe, NSW, Australia, 19-23 August 2014.

Unique evolution of D-conotoxins for defence

2013

Conference Publication

Discovery of novel spider peptides blocking hNav1.7

Cardoso, F. C., Herzig, V., Hauke, T., Lewis, R. J. and King, G. F. (2013). Discovery of novel spider peptides blocking hNav1.7. 3rd Annual Conference of the Toxinological Society of India and 1st International Conference on “Biology of Natural Toxins”, Goa, India, 19-21 December, 2013.

Discovery of novel spider peptides blocking hNav1.7

Funding

Current funding

  • 2023 - 2026
    Peptide Inhibitors Targeting Sodium Channels to Treat Amyotrophic Lateral Sclerosis
    United States Congressionally Directed Medical Research Programs - Amyotrophic Lateral Sclerosis Research Program
    Open grant

Past funding

  • 2020 - 2023
    Novel multifunctional analgesic sodium channel inhibitors
    NHMRC IDEAS Grants
    Open grant
  • 2018 - 2019
    Development of dual Nav1.1/1.7 inhibitors for the treatment of IBS-related pain
    UniQuest Pty Ltd
    Open grant

Supervision

Availability

Dr Fernanda Cardoso is:
Available for supervision

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

Available projects

  • We are seeking enthusiastic students to join our Lab! Please get in touch with us if you want to learn from our fantastic team at the Institute for Molecular Biosciences!

  • Discovery and characterization of bio-active molecules from animal venoms

    We have open positions for Research Students to develop projects in discovery, characterization and structure-function studies of bio-active compounds in animal venoms and other natural repertoires. Students will develop skills in high throughput cellular assays using fluorescence imaging assays, manual and automated whole-cell patch clamp electrophysiology, high performance liquid chromatography, mass spectometry, recombinant expression, peptide synthesis, amongst other state-of-the-art methods and techiniques. Students will also co-author papers and be involved in writting and figures preparation for research publications from their work.

  • Therapeutics development

    We have open positions for Research Students to develop projects in therapies for treating Chronic Pain, Visceral Pain and Motor Neuron Disease. These novel therapies will be developed from bio-active compounds targeting voltage-gated sodium and/or calcium channels. Students will develop skills in manual and automated whole-cell patch clamp electrophysiology, high performance liquid chromatography, mass spectometry, recombinant expression, peptide synthesis, amongst other state-of-the-art methods and techiniques. Students will also co-author papers and be involved in writting and figures preparation for research publications from their work.

  • Other research projects in HDR

    On-going

    Isolation and characterisation of novel analgesic conotoxins - Tianjiao Zhao Doctor Philosophy — Associate Advisor

    Completed

    The unexplored pharmacopeia of Australian spiders: learning from the experts - Hayden Wirth (2022) Science Honours — Principal Advisor

    Peptides targeting sodium channels to treat Motor Neuron Disease - Charan Kotapati (2022) Biomedical Sciences Honours — Principal Advisor

    Structure-Function and Rational Design of a Newly Discovered Spider Venom Peptide Ssp1a at hNaV1.2, hNaV1.3 and hNaV1.7 Yashad Dongol (2020) Doctor Philosophy — Associate Advisor

    Spider-venom peptides targeting ion channels in chronic pain pathways - Amatulla Shakir Nashikwala (2022) Master Coursework — Principal Advisor

    In vitro assessment of human neuroblastoma cytotoxicity induced by snake venoms - Simon Kramer (2022) Summer Research project — Principal Advisor

    Molecular pharmacology and peripheral analgesia of omega-conotoxins- Mahadhi Hasan (2021) Doctor Philosophy — Associate Advisor

    Discovery and Characterisation of Venom Peptide and Small Molecule Modulators for T-type Calcium Channels - Dan Wang (2020) Doctor Philosophy — Associate Advisor

    Molecular interactions between spider peptides and the sodium channel Nav1.1 - Huyiu Hu (2019) Masters Coursework — Principal Advisor

    Structure-function relatioships of the multifunctional spider peptide Tap1a - Saja E Mawlawi (2019) Masters Coursework — Principal Advisor

    Novel ion channels modulators from Australian tarantula venoms - Phil M Choin (2015) Summer Research Project — Associate Advisor

    N-type calcium channels modulators from Australian tarantula venoms - Wan Nur Amalina (2015) Summer Research Project — Associate Advisor

    Isolation and characterization of novel spider venom peptides antagonizing voltage-gated calcium channels - Ching Koon Lim (2014) Masters Coursework — Associate Advisor

    Optimizing the potency and selectivity of a spider-venom peptide that inhibits the analgesic target Nav1.7 - Andelain Erickson (2014) Honours — Associated Advisor

Supervision history

Current supervision

  • Doctor Philosophy

    Selective inhibition of voltage gated sodium channels using ProTx-III spider venom peptide to treat motor neuron disease

    Principal Advisor

    Other advisors: Professor Glenn King

  • Doctor Philosophy

    Venom variation in New World pit vipers

    Associate Advisor

    Other advisors: Dr Andrew Walker, Professor Bryan Fry

Completed supervision

Media

Enquiries

Contact Dr Fernanda Cardoso directly for media enquiries about:

  • Analgesics
  • Bio-active peptides
  • Drug discovery
  • Ion channels
  • Irritable bowel syndrome
  • Motor Neuron Disease
  • Neurodegeneration
  • Neurological disorders
  • Pain
  • Snake
  • Spider
  • Toxins
  • Venoms

Need help?

For help with finding experts, story ideas and media enquiries, contact our Media team:

communications@uq.edu.au