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Discovery Early Career Researcher Award - Grant ID: DE180100194
Funder
Australian Research Council
Funding Amount
$374,200.00
Summary
Quantitative three-dimensional imaging of membrane proteins. This project aims to address the challenge of in-situ quantification of membrane proteins through the emerging field of antibody-imaging mass spectrometry. The project will develop new protocols for quantitative three-dimensional imaging that aim to negate histological artifacts created by freeze-thaw and cryo-sectioning. Membrane proteins are involved in numerous cellular functions and this project expects to increase our knowledge o ....Quantitative three-dimensional imaging of membrane proteins. This project aims to address the challenge of in-situ quantification of membrane proteins through the emerging field of antibody-imaging mass spectrometry. The project will develop new protocols for quantitative three-dimensional imaging that aim to negate histological artifacts created by freeze-thaw and cryo-sectioning. Membrane proteins are involved in numerous cellular functions and this project expects to increase our knowledge of these fundamental biological processes by providing new insights into the study of these essential biomolecules. Tracking protein heterogeneity in three-dimensions will provide significant benefits to our understanding of systems biology and will benefit numerous area, including the pharmaceutical industry.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE170100092
Funder
Australian Research Council
Funding Amount
$372,000.00
Summary
X-ray induced photoacoustic nanoprobe: Break depth dependency of bioimaging. This project aims to develop a nanoprobe using an X-ray excited luminescence “nanolaser” as the local light source to activate coupled responsive photoacoustic sensors. In-situ imaging of specific biomarkers at the molecular level is key to understanding their roles in physiological and pathological processes, but current imaging techniques using fluorescent probes cannot detect biomarkers in deep tissues due to shallow ....X-ray induced photoacoustic nanoprobe: Break depth dependency of bioimaging. This project aims to develop a nanoprobe using an X-ray excited luminescence “nanolaser” as the local light source to activate coupled responsive photoacoustic sensors. In-situ imaging of specific biomarkers at the molecular level is key to understanding their roles in physiological and pathological processes, but current imaging techniques using fluorescent probes cannot detect biomarkers in deep tissues due to shallow light penetration. By capitalising on the tissue penetrating property of X-rays and acoustic waves and collecting acoustic waves as the read-out signal, real-time monitoring of biomarkers in deep tissues could be achieved, advancing detection technology for deep-tissue biomarkers.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE220100311
Funder
Australian Research Council
Funding Amount
$383,982.00
Summary
Shining nanoparticles for single microRNA detection in microfluidics. This project aims to extensively study the interface between nanoparticles and nucleic acids. It sets out to produce a novel ultrasensitive high-performance biosensing platform that will combine luminescent nanoparticles with microfluidics in a digital assay. This portable platform will detect biological fingerprints, or microRNAs, at a single-molecule level, delivering unprecedented levels of sensitivity and specificity. The ....Shining nanoparticles for single microRNA detection in microfluidics. This project aims to extensively study the interface between nanoparticles and nucleic acids. It sets out to produce a novel ultrasensitive high-performance biosensing platform that will combine luminescent nanoparticles with microfluidics in a digital assay. This portable platform will detect biological fingerprints, or microRNAs, at a single-molecule level, delivering unprecedented levels of sensitivity and specificity. The multiplexed platform has the potential to benefit the biomedical research of microRNAs and opens up a genuine commercialisation potential for portable biosensing of nucleic acids.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE150101243
Funder
Australian Research Council
Funding Amount
$371,000.00
Summary
The molecular mechanisms of dual nucleic acid specificities of SFPQ. Dynamic interactions between proteins and nucleic acids are a fundamental process in gene regulation, where aberrant regulation leads to lethality or various diseases. This project aims to elucidate the underlying mechanisms of DNA-RNA interplay with a multifunctional nuclear protein, splicing factor proline/glutamine-rich (SFPQ) in gene regulation at the molecular level by characterising the interactions between SFPQ and nucle ....The molecular mechanisms of dual nucleic acid specificities of SFPQ. Dynamic interactions between proteins and nucleic acids are a fundamental process in gene regulation, where aberrant regulation leads to lethality or various diseases. This project aims to elucidate the underlying mechanisms of DNA-RNA interplay with a multifunctional nuclear protein, splicing factor proline/glutamine-rich (SFPQ) in gene regulation at the molecular level by characterising the interactions between SFPQ and nucleic acids. The results will provide a fundamental understanding of the molecular mechanisms of dual nucleic acid specificities of nuclear proteins in gene regulation, for which no structural information is currently available.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE180100080
Funder
Australian Research Council
Funding Amount
$365,058.00
Summary
Examining lipid transport by direct visualisation and quantification. This project aims to investigate the least understood aspect of plasma triglyceride metabolism; mechanisms of transport across capillary endothelial cells. This transport regulates plasma triglyceride levels, which are an important factor in determining risk for coronary diseases. An improved understanding of these mechanisms will lead in the long term to better understandings of both heart failure and atherosclerotic heart di ....Examining lipid transport by direct visualisation and quantification. This project aims to investigate the least understood aspect of plasma triglyceride metabolism; mechanisms of transport across capillary endothelial cells. This transport regulates plasma triglyceride levels, which are an important factor in determining risk for coronary diseases. An improved understanding of these mechanisms will lead in the long term to better understandings of both heart failure and atherosclerotic heart diseases.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE150101863
Funder
Australian Research Council
Funding Amount
$372,000.00
Summary
Strained alkenes as chemical probes for cysteine sulfenic acid. This project aims to introduce strained alkenes as probes for cysteine sulfenic acid, a poorly understood biomarker for oxidative stress. This probe will enable rapid detection of cysteine sulfenic acid and meet an urgent need for tools to map cysteine redox signalling. Moreover, since many enzymes feature a cysteine sulfenic acid at their active site, the strained alkene probes will also serve as useful inhibitor probes of these en ....Strained alkenes as chemical probes for cysteine sulfenic acid. This project aims to introduce strained alkenes as probes for cysteine sulfenic acid, a poorly understood biomarker for oxidative stress. This probe will enable rapid detection of cysteine sulfenic acid and meet an urgent need for tools to map cysteine redox signalling. Moreover, since many enzymes feature a cysteine sulfenic acid at their active site, the strained alkene probes will also serve as useful inhibitor probes of these enzymes. Such inhibitor probes will provide critical information for potential therapeutic applications in human conditions associated with oxidative stress such as ageing, cancer, and heart disease.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE180100859
Funder
Australian Research Council
Funding Amount
$365,058.00
Summary
Phosphatidylserine: a regulator of muscle and mitochondrial biology? This project aims to characterise a novel pathway involved in regulating skeletal muscle mass through effects on mitochondrial function. This project will examine how degradation causes mitochondrial abnormalities leading to severe muscle wasting. This project is expected to advance understanding of how pathways interact, thus identifying novel mechanisms that impact on muscle structure and function. Understanding what makes mu ....Phosphatidylserine: a regulator of muscle and mitochondrial biology? This project aims to characterise a novel pathway involved in regulating skeletal muscle mass through effects on mitochondrial function. This project will examine how degradation causes mitochondrial abnormalities leading to severe muscle wasting. This project is expected to advance understanding of how pathways interact, thus identifying novel mechanisms that impact on muscle structure and function. Understanding what makes muscle vulnerable to atrophy is fundamental to developing strategies to counteract muscle wasting conditions. Methodologies developed will have broad application in the field of life sciences research.Read moreRead less
Discovery Early Career Researcher Award - Grant ID: DE170100058
Funder
Australian Research Council
Funding Amount
$372,000.00
Summary
Molecular reporters for measuring proteostasis capacity in cells. This project aims to develop fluorescent dyes to report on the change in unfolded protein load, which reflects the proteostasis status in real time in cells under stress conditions. Proteostasis is a housekeeping process cells undertake to maintain the proper folding and functions of proteins. Perturbation of proteostasis has been linked to neurodegenerative diseases, but chemical probes cannot measure the proteostasis capacity in ....Molecular reporters for measuring proteostasis capacity in cells. This project aims to develop fluorescent dyes to report on the change in unfolded protein load, which reflects the proteostasis status in real time in cells under stress conditions. Proteostasis is a housekeeping process cells undertake to maintain the proper folding and functions of proteins. Perturbation of proteostasis has been linked to neurodegenerative diseases, but chemical probes cannot measure the proteostasis capacity in cells. Intended outcomes include a mechanistic understanding of the relationship between protein misfolding, aggregation and proteostasis. This is expected to ultimately benefit the diagnosis of protein folding diseases, including dementia, and improve the quality of life.Read moreRead less