Scientific Interests

Key Skills and Knowledge Areas

Medicinal Chemistry
  • Therapeutics development via Organic Chemistry (specialty in radioprosthetic, chelator, amino acid and nucleotide development)
  • Synthetic route design and optimization
  • Bioconjugation (small molecules payloads, linkers, oligonucleotides, peptides, antibodies)
  • Solid phase peptide synthesis (standard and custom amino acids, manual and automatic, linear and cyclic)
  • Biomolecule library development through computational modelling, databases and structural activity relationship (SAR)
  • Validation via mass spectroscopy (MS, including MALDI), inductively coupled plasma (ICP-MS, ICP-OES), high performance liquid chromatography (HPLC, including LC-MS), nuclear magnetic spectroscopy (NMR), surface plasmon resonance (SPR), infra-red spectroscopy (FTIR-ATR), X-ray crystallography (XRD)
  • I also teach some of these topics in UBC Chemistry course CHEM461+561.
Radiochemistry
  • Radioisotopes: 18F, 32P, 68Ga, 111In, 161Tb, 177Lu, and more
  • Protein (including antibodies) and peptide radioconjugates (includes chelators)
  • Oligonucleotide and nucleotide chelator radioconjugates (includes chelators)
  • Radiobiocatalysis (specialty in oligonucleotide biochemistry)
  • Labeling conditions and assay development
  • Quality control data and troubleshoot radiosyntheses
  • Method development and optimization
  • Inventory, shipment, and containment management
Molecular Biology
  • Functional (biological) assay development (e.g. MTT/MTS, ELISA, lentivirus, binding assays)
  • Culturing (bacterial, mammalian) and sterile workflows
  • Enzymology (specialty in nucleic acid-modifying enzymes)
  • Oligonucleotide manipulation and purification (includes HPLC)
  • Microscopy
  • Lentivirus manipulation
  • I also teach some of these topics in UBC Biochemistry course BIOC301.
Pre-clinical Comparative Nuclear Medicine
  • Positron Emission Tomography (PET) scan processing and analysis
  • Rodent restraint
  • Subcutaneous and intraperitoneal injections
  • Biodistribution analysis
Academic Communication
  • Scientific artwork (Adobe Illustrator + InDesign)
  • Webpage design (WordPress)
  • Technical writing
    • Peer-reviewed articles
    • Technology transfer documents
  • Scientific instruction at university level
Personal Attributes
  • Project leadership and collaboration across multi-disciplinary boundaries
  • Autonomous experimental design and execution
  • Robust collaboration, negotiation, and problem solving
  • Coaching and advising young scientists through facilitation
  • Fluency in English
Knowledge Areas
  • Chemical biology
  • Biochemistry
  • Pharmaceutical industry and business opportunity translation (specialty in radiopharmaceuticals)
  • Oncology (specialty in nuclear medicine)
  • Pharmacokinetics

As evidence of demonstrating these skills, the complete list of publications is available here.

Modification of Nucleotides for Biological Recognition

My research focuses on the chemical biology of nucleotides, exploring modifications to enhance their molecular targeting capacities and biological stability. This work is particularly relevant in advancing medical applications, as exemplified by approval of nucleic acid-based medicines such as vaccines, aptamer drugs, and nucleotide analogs.

Medical Imaging

My first leading-author publication on positron emission tomography (PET) targeting thymidine metabolism in colorectal cancer.

DNAzyme Selection

Modification of nucleotide triphosphates leads to selection of DNAzymes that cleaves specific RNA sequences.

Development of Peptide Inhibitor Theranostics for Pre-clinical Cancer Care

In response to the persistent public health challenge posed by cancer, our research team is developing peptide inhibitor radiopharmaceuticals by integrating diagnostic and therapeutic radioisotopes (i.e. theranostics). Building on the FDA approval of Prostate Membrane Specific Antigen (PSMA)-specific radiotracers, we aim to enhance the chemical libraries of PSMA and Fibroblast Activation Protein (FAP) inhibitors (FAPI) to optimize in vivo performance. This collaborative holds promising potential for translation to human clinical trials, such as prostate and colorectal cancer.

PSMA Analogs with clinically impactful biodistribution

Careful choice of amino acid in PSMA analogs reduces salivary gland uptake.

Novel Tricyclic FAPI Analogs

Exploring novel tricyclic FAPI analogs with sustained radiotracer tumor uptake.

Structural Activity Relationship of Small Molecule Inhibitors

My work delves into the structural activity relationship of small molecule inhibitors, with a focus on α-amanitin, a potent neurotoxin isolated from the death cap mushroom Amanita phalloides. Leveraging the first total synthesis of amanitin, I aim to explore its close analogs to identify more potent toxins for targeted cancer therapy, tapping into the immense potential of natural products as potent drugs.

Novel antibody-amanitin conjugates

By studying the hydroxy-proline residue, novel antibody-drug conjugates (ADCs) with synthetic amanitin analogs were tested in vitro for the first time.

Supratoxic analogs rival the natural product

Novel amanitin analogs were found more potent than the naturally found α-amanitin through modification of the eastern-ring.

Complete list of publications is available here.

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