Post Doctoral Associate
University of Pittsburgh
Postdoctoral Associate Molecular/structural Biology, GPCR Biology, Organoids, RNA-seq, and AI ML /DL-driven Drug Discovery Recruitment focus: molecular biology, structural pharmacology by cryo-EM and X-ray crystallography, baculovirus/Sf9 expression of GPCRs, RNA-sequencing, kidney organoids, SQSTM1/p62-targeted drug MOA studies in multiple myeloma, cannabinoid receptor CB2 pharmacology, and AI/ML/DL approaches. Position Overview The Xie Laboratory at the University of Pittsburgh School of Pharmacy seeks a highly motivated Postdoctoral Associate or Lab Researcher (PhD or equivalent; exceptional MS-level candidates with relevant experience may also be considered) to join a multidisciplinary research program integrating molecular biology, structural pharmacology, receptor biology, organoid models, RNA-sequencing, and AI/ML-enabled drug discovery. The successful candidate will help advance the lab’s programs centered on cannabinoid receptor CB2 signaling and pharmacology, GPCR structural biology, SQSTM1/p62-targeted small-molecule drug mechanism-of-action studies for multiple myeloma, and kidney organoid models for translational research. The laboratory builds on its published work in the 3D cryo-EM structure of the human CB2-Gi signaling complex (Cell, 2020; PMID: 32004460) and generative AI modeling for drug design and discovery (Cells, 2022; PMID: 35269537). More information about the lab is available at CBIDDell22.pharmacy.pitt.edu Ideal Candidate Profile (in one of the fields)
- Strong training in molecular biology, biochemistry, biophysics, pharmacology, structural biology, bioinformatics, computational biology, AI/data science, or a closely related field.
- Hands-on experience with GPCR biology, receptor pharmacology, protein expression & purification, and cell-based functional assays is highly desirable.
- Experience in human organoid and disease-model research, for example in kidney or oncology organoid model development and translational pharmacology.
- Experience with cryo-electron microscopy, X-ray crystallography, or integrative structural pharmacology approaches is strongly preferred.
- Experience with baculovirus/Sf9 expression systems for GPCRs or other membrane proteins is a major advantage.
- Interest or experience in RNA-sequencing, single-cell or bulk transcriptomics, pathway analysis, and bioinformatics-driven mechanism-of-action studies is desirable.
- Interest or experience in human kidney organoids, disease modeling, fibrosis biology, or target-specific drug MOA validation is a plus.
- Ability to work independently while contributing effectively to a multidisciplinary team spanning experimental biology, computational modeling, and translational drug discovery.
- Molecular biology and cell signaling: Design and execute experiments involving cloning, site-directed mutagenesis, CRISPR/Cas9-based approaches, receptor signaling assays, binding assays, and cellular functional assays.
- Structural pharmacology: Support structural studies of GPCRs and signaling complexes using cryo-EM, X-ray crystallography, biochemical characterization, and structure-guided pharmacology.
- GPCR expression and purification: Develop and optimize baculovirus/Sf9 expression, membrane protein production, purification workflows, and quality-control assays for cannabinoid receptor CB2 and related GPCR targets.
- Human organoid and disease-model research: Contribute to kidney or oncology organoid model development and target-specific drug MOA studies relevant to fibrosis oncology translational pharmacology.
- Hematological malignancy drug MOA: I nvestigate SQSTM-1/p62-targeted small-molecule or antibody autophagy cell data, decision and cell signaling studies for mechanisms of action in acute myeloid leukemia (AML), multiple myeloma (MM), kidney fibrosis, Alzheimer’s disease, hematopoietic stem cells, and osteoporosis by using molecular, cellular, and omics-based approaches.
- RNA-seq and bioinformatics: Generate, analyze, and interpret bulk, single-cell, single-nucleus, or network RNA-seq data to define drug response, pathway modulation, and disease-relevant mechanisms.
- AI/ML/DL and computational drug discovery: Collaborate on AI, machine learning, deep learning, chemogenomics, graph neural networks, generative modeling, and structure-based drug-discovery workflows.
- Candidates with Web/mobile app development, data analytics, network information security, GUI design, proficiency in at least one object-oriented programming language (e.g., Java, C++, or C#), and scripting language (e.g., Python, PHP) will also be considered
- Communication and mentorship: Prepare manuscripts, grant materials, presentations, and research reports; maintain organized records; and assist the PI in mentoring graduate students and junior lab researchers.
- PhD or equivalent experience in molecular biology, biochemistry, biophysics, pharmacology, structural biology, bioinformatics, computational biology, AI/data science, computer science, or a related field.
- Demonstrated ability to conduct independent and innovative research, analyze data rigorously, and communicate findings clearly in written and oral formats.
- Strong scientific writing skills, attention to detail, and ability to prepare manuscripts, grant-related materials, and technical reports.
- Experience with BSL2 or BSL2+ cell culture, receptor pharmacology assays, protein-expression systems, or omics data analysis is preferred.
- Experience with Python, R, molecular modeling, structural analysis, or AI/ML/DL workflows is a plus.
- A collaborative mindset and strong interpersonal skills for working in an interdisciplinary academic and translational research environment.
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