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Jinghang Xie

Jinghang Xie

Assistant Professor, Molecular Physiology and Biological Physics

Primary Location
Sheridan G. Snyder Translational Research Building
480 Ray C. Hunt Dr
Charlottesville, VA 22903
Primary Phone Number

Bio & Overview

We forge collaborative efforts at the dynamic intersection of biology, chemistry, and medicine, propelling forward the boundaries of scientific exploration. Our work revolves around the development of cutting-edge imaging tools, empowering us to unravel the intricate mechanisms underlying immunological responses to vaccines and therapies. Through our innovative approaches, we enable visualization and delve deep into the core of these phenomena, shedding light on their workings and opening new avenues for discovery and breakthroughs.

Academic Information

Department
Molecular Physiology and Biological Physics

Primary Education

  • PhD, Pharmaceutical and Chemical Sciences, University of the Pacific, 2014
  • Postdoc, Chemical Biology, Stanford University, 2022

Research Interests

Molecular Imaging; Cancer Immunology; Vaccines.

Research Disciplines

  • Biochemistry
  • Biophysics & Structural Biology
  • Biotechnology
  • Cancer Biology
  • Chemical Engineering
  • Immunology
  • Molecular Physiology and Biological Physics

Research Opportunities

  • Biochemistry
  • Biophysics & Structural Biology
  • Biotechnology
  • Cancer Biology
  • Cancer Immunology and Immunotherapy
  • Chemistry and Physics of Living Systems
  • Immunology
  • Infectious Diseases

PhD Programs

  • Biophysics
  • Physiology

Selected Publications

2023

Dai, T., Xie, J., Buonomo, J. A., Moreno, A., Banaei, N., Bertozzi, C. R., & Rao, J. (2023). Bioluminogenic Probe for Rapid, Ultrasensitive Detection of ?-Lactam-Resistant Bacteria. ANALYTICAL CHEMISTRY, 95(18), 7329-7335. doi:10.1021/acs.analchem.3c00478

Yin, Q., Luo, W., Mallajosyula, V., Bo, Y., Guo, J., Xie, J., . . . Davis, M. M. M. (2023). A TLR7-nanoparticle adjuvant promotes a broad immune response against heterologous strains of influenza and SARS-CoV-2. NATURE MATERIALS, 22(3), 380-+. doi:10.1038/s41563-022-01464-2

2022

Chen, M., Zhou, K., Dai, S. -Y., Tadepalli, S., Balakrishnan, P. B., Xie, J., . . . Rao, J. (2022). In vivo bioluminescence imaging of granzyme B activity in tumor response to cancer immunotherapy. CELL CHEMICAL BIOLOGY, 29(10), 1556-+. doi:10.1016/j.chembiol.2022.08.006

Xie, J., El Rami, F., Zhou, K., Simonetta, F., Chen, Z., Zheng, X., . . . Rao, J. (2022). Multiparameter Longitudinal Imaging of Immune Cell Activity in Chimeric Antigen Receptor T Cell and Checkpoint Blockade Therapies. ACS CENTRAL SCIENCE, 8(5), 590-602. doi:10.1021/acscentsci.2c00142

2021

Xie, J., Mu, R., Fang, M., Cheng, Y., Senchyna, F., Moreno, A., . . . Rao, J. (2021). A dual-caged resorufin probe for rapid screening of infections resistant to lactam antibiotics. CHEMICAL SCIENCE, 12(26), 9153-9161. doi:10.1039/d1sc01471d

Chen, M., Chen, Z., Castillo, J. B., Cui, L., Zhou, K., Shen, B., . . . Rao, J. (2021). [18F]-C-SNAT4: an improved caspase-3-sensitive nanoaggregation PET tracer for imaging of tumor responses to chemo- and immunotherapies. EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 48(11), 3386-3399. doi:10.1007/s00259-021-05297-0

Xie, J., Rice, M. A., Chen, Z., Cheng, Y., Hsu, E. -C., Chen, M., . . . Rao, J. (2021). In Vivo Imaging of Methionine Aminopeptidase II for Prostate Cancer Risk Stratification. CANCER RESEARCH, 81(9), 2510-2521. doi:10.1158/0008-5472.CAN-20-2969

2020

Cui, L., Gouw, A. M., LaGory, E. L., Guo, S., Attarwala, N., Tang, Y., . . . Rao, J. (2021). Mitochondrial copper depletion suppresses triple-negative breast cancer in mice. NATURE BIOTECHNOLOGY, 39(3), 357-367. doi:10.1038/s41587-020-0707-9

Dai, T., Xie, J., Zhu, Q., Kamariza, M., Jiang, K., Bertozzi, C. R., & Rao, J. (2020). A Fluorogenic Trehalose Probe for Tracking Phagocytosed Mycobacterium tuberculosis. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 142(36), 15259-15264. doi:10.1021/jacs.0c07700

Chen, Z., Chen, M., Cheng, Y., Kowada, T., Xie, J., Zheng, X., & Rao, J. (2020). Exploring the Condensation Reaction between Aromatic Nitriles and Amino Thiols To Optimize In Situ Nanoparticle Formation for the Imaging of Proteases and Glycosidases in Cells. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 59(8), 3272-3279. doi:10.1002/anie.201913314

2018

Cheng, Y., Xie, J., Lee, K. -H., Gaur, R. L., Song, A., Dai, T., . . . Rao, J. (2018). Rapid and specific labeling of single live Mycobacterium tuberculosis with a dual-targeting fluorogenic probe. SCIENCE TRANSLATIONAL MEDICINE, 10(454). doi:10.1126/scitranslmed.aar4470

2017

Song, A., Cheng, Y., Xie, J., Banaei, N., & Rao, J. (2017). Intramolecular substitution uncages fluorogenic probes for detection of metallo-carbapenemase-expressing bacteria. CHEMICAL SCIENCE, 8(11), 7669-7674. doi:10.1039/c7sc02416a

2016

Zheng, Y., Xie, J., Huang, X., Dong, J., Park, M. S., & Chan, W. K. (2016). Binding studies using Pichia pastoris expressed human aryl hydrocarbon receptor and aryl hydrocarbon receptor nuclear translocator proteins. PROTEIN EXPRESSION AND PURIFICATION, 122, 72-81. doi:10.1016/j.pep.2016.02.011

2015

Penchala, S. C., Miller, M. R., Pal, A., Dong, J., Madadi, N. R., Xie, J., . . . Alhamadsheh, M. M. (2015). A biomimetic approach for enhancing the in vivo half-life of peptides. NATURE CHEMICAL BIOLOGY, 11(10), 793-+. doi:10.1038/NCHEMBIO.1907

Lyu, F., Xu, M., Cheng, Y., Xie, J., Rao, J., & Tang, S. K. Y. (2015). Quantitative detection of cells expressing BlaC using droplet-based microfluidics for use in the diagnosis of tuberculosis. BIOMICROFLUIDICS, 9(4). doi:10.1063/1.4928879

2014

Xie, J., Huang, X., Park, M. S., Pham, H. M., & Chan, W. K. (2014). Differential suppression of the aryl hydrocarbon receptor nuclear translocator-dependent function by an aryl hydrocarbon receptor PAS-A-derived inhibitory molecule. BIOCHEMICAL PHARMACOLOGY, 88(2), 253-265. doi:10.1016/j.bcp.2014.01.021

2010

Park, M. S., Chu, F., Xie, J., Wang, Y., Bhattacharya, P., & Chan, W. K. (2011). Identification of cyclophilin-40-interacting proteins reveals potential cellular function of cyclophilin-40. ANALYTICAL BIOCHEMISTRY, 410(2), 257-265. doi:10.1016/j.ab.2010.12.007