About
My research interests encompass molecular biology, protein biochemistry, and structural biology, with a focus on understanding protein degradation mechanisms, particularly within the Proteasome Degradation machinery. I specialize in investigating degradation kinetics, substrate recognition, ubiquitination, and proteolysis, alongside the regulatory role of post-translational modifications in protein turnover. Proficient in molecular cloning, protein purification, immuno-blotting, and multi-angle light scattering, I have recently expanded into cryo-electron microscopy (cryoEM) for unraveling the structural intricacies of the 26S proteasome. Committed to promoting scientific collaboration and open access, I actively engage in conferences, workshops, and collaborative projects to foster knowledge exchange within the scientific community, maintaining an updated ORCID record to reflect my contributions and achievements accurately
Employment
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NCI-NIH Postdoc Fellow2021 - Present
Education
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National Centre for Biological Sciences Doctoral2015 - 2021
Projects & Funding
Projects & funding information is unavailable.
Publications (11)
- Investigating Enzyme-Substrate Interactions in the Assembly of K48/K63 Heterotypic Ubiquitin Chains Save
- Proteasome activity maintains cell-type-specific gene expression Save
- Structures of dynamic interactors at native proteasomes by PhIX-MS and cryoelectron microscopy Save
- An adaptive peptide-binding site in ubiquitin receptor hRpn13 revealed by structural studies. Save
- CD28 hinge used in chimeric antigen receptor (CAR) T-cells exhibits local structure and conformational exchange amidst global disorder. Save
- Plasticity of the proteasome-targeting signal Fat10 enhances substrate degradation Save
- An engineered cell line with a hRpn1-attached handle to isolate proteasomes Save
- A novel polyubiquitin chain linkage formed by viral Ubiquitin is resistant to host deubiquitinating enzymes Save
- The Viral SUMO–Targeted Ubiquitin Ligase ICP0 is Phosphorylated and Activated by Host Kinase Chk2 Save
- A five-residue motif for the design of domain swapping in proteins Save