Wikipedia

Ying Ge

Ying Ge is a Chinese-American chemist who is a Professor of Cell and Regenerative Biology at the University of Wisconsin–Madison. Her research considers the molecular mechanisms that underpin cardiac disease. She has previously served on the board of directors of the American Society for Mass Spectrometry. In 2020 Ge was named on the Analytical Scientist Power List.

Ying Ge
Alma materCornell University
University of Peking
Scientific career
InstitutionsUniversity of Wisconsin-Madison
Wyeth
ThesisTop down characterization of proteins by electron capture dissociation and blackbody infrared radiative dissociation mass spectrometry (2002)

Early life and education

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Ge was born in China. She attended Peking University for her undergraduate studies, where she studied chemistry.[1] After graduating in 1997 Ge moved to the United States, where she joined Cornell University as a doctoral student.[1] Here she started to work on mass spectrometry, using electron-capture dissociation to study proteins.[2] She worked under the supervision of Tadhg Begley and Fred McLafferty. After completing her doctorate, Ge worked as a research scientist at Wyeth.[citation needed]

Research and career

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Ge joined the University of Wisconsin–Madison as an assistant scientist, where she oversaw the mass spectrometry programme. She became an Associate Professor in 2015, and full Professor in 2019.[3]

Ge develops high-resolution mass spectrometry proteomics to better understand cardiac disease. To image the very large proteins of human heart tissue, Ge combines fourier-transform ion cyclotron resonance (FT–ICR) mass spectrometry with electron-capture dissociation.[4] She has worked to create a top-down disease proteomic platform that allows for the separation, detection and characterisation of the biomarkers of heart damage.

Nanoproteomics, a technique developed by Ge and co-workers, makes use of nanoparticles and high resolution mass spectrometry to capture and characterise cardiac troponins, including troponin I.[5][6] Being able to test for and characterise troponin I would help with the early detection and diagnosis of heart disease.[7] The peptide-functionalised superparamagnetic nanoparticles are combined with top-down mass spectrometry to identify the molecular fingerprints of troponins.[7] Rather than just detecting cardiac troponins, which is possible using ELISA-based antibody testing, this higher level of characterisation will allow Ge to identify various forms of modified troponins, allowing a personalised understanding of cardiac disease.[7]

Ge served on the board of the Top-Down Proteomics Consortium,[8] on the editorial board of the Journal of Muscle Research and Cell Motility,[9] as treasurer for the American Society for Mass Spectrometry (2016-2018).[10]

Ying Ge publications indexed by Google Scholar.

Awards and honours

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Selected publications

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  • Smith, Lloyd M; Kelleher, Neil L (2013-02-27). "Proteoform: a single term describing protein complexity". Nature Methods. 10 (3): 186–187. doi:10.1038/nmeth.2369. ISSN 1548-7091. PMC 4114032. PMID 23443629.
  • Ge, Ying; Lawhorn, Brian G.; ElNaggar, Mariam; Strauss, Erick; Park, Joo-Heon; Begley, Tadhg P.; McLafferty, Fred W. (2002-01-01). "Top Down Characterization of Larger Proteins (45 kDa) by Electron Capture Dissociation Mass Spectrometry". Journal of the American Chemical Society. 124 (4): 672–678. doi:10.1021/ja011335z. ISSN 0002-7863. PMID 11804498.
  • Horn, David M.; Ge, Ying; McLafferty, Fred W. (2000-10-01). "Activated Ion Electron Capture Dissociation for Mass Spectral Sequencing of Larger (42 kDa) Proteins". Analytical Chemistry. 72 (20): 4778–4784. doi:10.1021/ac000494i. ISSN 0003-2700. PMID 11055690.
  • Sze, Siu Kwan; Ge, Ying; Oh, HanBin; McLafferty, Fred W. (2002-02-19). "Top-down mass spectrometry of a 29-kDa protein for characterization of any posttranslational modification to within one residue". Proceedings of the National Academy of Sciences. 99 (4): 1774–1779. doi:10.1073/pnas.251691898. ISSN 0027-8424. PMC 122269. PMID 11842225.

References

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  1. ^ a b "yge | Department of Chemistry". www2.chem.wisc.edu. Retrieved 2020-10-18.
  2. ^ Ge, Ying (2002). Top down characterization of proteins by electron capture dissociation and blackbody infrared radiative dissociation mass spectrometry (Thesis). OCLC 52791635.
  3. ^ "Ying Ge". HUPO Connect 2020. Retrieved 2021-10-31.
  4. ^ a b "Biemann Medal". www.asms.org. Retrieved 2020-10-18.
  5. ^ "New Nanoparticle Technology Reveals Common Marker of Heart Disease". AZoNano.com. 2020-08-07. Retrieved 2020-10-19.
  6. ^ "Nanoparticle system captures heart-disease biomarker from blood for in-depth analysis". phys.org. Retrieved 2020-10-19.
  7. ^ a b c "Biomarker for Heart Disease Captured by Novel Nanoparticle Technology". GEN - Genetic Engineering and Biotechnology News. 2020-08-07. Retrieved 2020-10-19.
  8. ^ "Board of Directors – Consortium for Top-Down Proteomics". Retrieved 2021-10-31.
  9. ^ "Journal of Muscle Research and Cell Motility". Springer. Retrieved 2021-10-31.
  10. ^ Brodbelt, Jenny; Li, Lingjun (2021-08-23). "Editorial: Focus on Top-Down Proteomics: Technology Advances and Biomedical Applications, Honoring Dr. Ying Ge, Recipient of the 2020 ASMS Biemann Medal". Journal of the American Society for Mass Spectrometry. 33 (9): 1586–1589. doi:10.1021/jasms.1c00209. ISSN 1044-0305. PMID 34423982. S2CID 237268712.
  11. ^ "Ying Ge Receives Georges Guiochon Faculty Fellowship at HPLC 2016". Chromatography Online. 22 June 2016. Retrieved 2020-10-18.
  12. ^ "Dr. Ying Ge awarded H.I. Romnes Faculty Fellowship". Molecular and Cellular Pharmacology Training Program. 2018-03-15. Retrieved 2020-10-18.
  13. ^ "The Power List 2019". The Analytical Scientist. Retrieved 2022-12-27.
  14. ^ "Ying Ge". The Analytical Scientist. Retrieved 2020-10-18.
  15. ^ "HUPO - 2021 HUPO Awards". hupo.org. Retrieved 2021-10-31.
  16. ^ "The Power List 2021". The Analytical Scientist. Retrieved 2022-12-27.
  17. ^ "The Power List 2024". The Analytical Scientist. 2024-08-17. Retrieved 2024-08-24.
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