Personal profile
Research interests
The shape of cellular membranes is a well-conserved evolutionary phenotype. Membrane shape is generated and maintained by the interplay between proteins and lipids and between lipids themselves. The detection and remodeling of membrane shapes are part of many essential cellular processes such as endocytosis, vesiculation, and protein trafficking.
Research in Dr. Fang Tian's lab has focused on understanding the structural and molecular mechanisms underlying the recognition and generation of membrane architecture and, in turn, how membrane structure determines protein localization and function using biochemical and biophysical analyses and nuclear magnetic resonance (NMR) spectroscopy. The lab has extended its exploration beyond a prototype membrane curvature-sensing bacterial proteins to human proteins that are key players in the biogenesis of the autophagosome during autophagy. Autophagy plays a significant role in the progression and outcome of numerous diseases, most notably neurodegeneration, infection, obesity and cancers.
The vision of Dr. Tian's research is that understanding the mechanics of the membrane structure and function as they relate to the biogenesis of the autophagosome will lead to new therapeutic strategies for the prevention and treatment of many human ailments.
Education/Academic qualification
Complex Carbohydrate Research Center, Postdoctoral Research Associate Fellowship, University of Georgia
1998 → 2001
PhD, Florida State University
1992 → 1998
BS, East China Normal University
1984 → 1989
Expertise related to UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
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SDG 3 Good Health and Well-being
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Collaborations and top research areas from the last five years
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Blocking autophagosome closure manifests the roles of mammalian Atg8-family proteins in phagophore formation and expansion during nutrient starvation
Bui, V., Liang, X., Ye, Y., Giang, W., Tian, F., Takahashi, Y. & Wang, H. G., 2025, In: Autophagy. 21, 5, p. 1059-1074 16 p.Research output: Contribution to journal › Article › peer-review
Open Access5 Link opens in a new tab Scopus citations -
DBeQ derivative targets vacuolar protein sorting 4 functions in cancer cells and suppresses tumor growth in mice
Fundora, K. A., Zhuang, Y., Hamamoto, K., Wang, G., Chen, L., Hattori, T., Liang, X., Bao, L., Vangala, V., Tian, F., Takahashi, Y. & Wang, H. G., Apr 2025, In: Journal of Pharmacology and Experimental Therapeutics. 392, 4, 103524.Research output: Contribution to journal › Article › peer-review
Open Access2 Link opens in a new tab Scopus citations -
Towards complete suppression of diagonal peaks in solid-state MAS NMR homonuclear chemical shift correlation spectra
Zhang, S., Li, Y., Ye, Y., Tian, F., Peng, X. & Fu, R., Sep 2025, In: Journal of Magnetic Resonance. 378, 107926.Research output: Contribution to journal › Article › peer-review
1 Link opens in a new tab Scopus citations -
Identification of membrane curvature sensing motifs essential for VPS37A phagophore recruitment and autophagosome closure
Ye, Y., Liang, X., Wang, G., Bewley, M. C., Hamamoto, K., Liu, X., Flanagan, J., Wang, H.-G., Takahashi, Y. & Tian, F., Dec 2024, In: Communications Biology. 7, 1, 334.Research output: Contribution to journal › Article › peer-review
Open Access8 Link opens in a new tab Scopus citations -
What’s in an E3: role of highly curved membranes in facilitating LC3–phosphatidylethanolamine conjugation during autophagy
Ye, Y., Bewley, M. C., Wang, H. G., Tian, F. & Flanagan, J. M., 2024, In: Autophagy. 20, 3, p. 709-711 3 p.Research output: Contribution to journal › Article › peer-review
Open Access6 Link opens in a new tab Scopus citations