Author

F. Teng

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Biochemistry· 2 Cancer Biology· 1 Cell Biology· 1 Immunology· 1 Microbiology· 1 Paleontology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 5 Research Focus:cell type annotation· 4 Organism:human· 3 Assay:proteomics· 3 Approach:statistical model· 2 Organism:C. elegans· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell-cell communication· 1

Frequent Co-Authors

X. Liu· 2 shared X. Xu· 2 shared Y. Li· 2 shared A. Chen· 1 shared B. Luo· 1 shared C. Huang· 1 shared C. Liu· 1 shared C. May· 1 shared

Activity by Year

2020-2023 · peak 4/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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2 shared papersCancer Biology

X. Liu

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Author profile →

7 papers

Recent·Most cited

A Synthetic Cytotoxic T cell Platform for Rapidly Prototyping TCR Function

G. Sharma, J. Round, F. Teng, Z. Ali, C. May, E. Yung, R. Holt

This paper introduces a synthetic cytotoxic T cell platform for rapidly prototyping TCR function, demonstrating successful antigen-specific responses and preservation of antigen-presenting cells.

bioRxiv · Nov 20, 2023Immunology

StereoSiTE: A framework to spatially and quantitatively profile the cellular neighborhood organized iTME

X. Liu, C. Qu, C. Liu, N. Zhu, H. Huang, F. Teng, C. Huang, B. Luo, X. Liu, Y. Xu, M. Xie, F. Xi, M. Li, L. Wu, Y. Li, , J. Zhang

StereoSiTE analyzes spatial transcriptomics data to identify cell-cell interactions in the tumor microenvironment and reveals neutrophil-driven communication networks in treated xenograft models.

bioRxiv · Dec 31, 2022Cancer Biology

Structural basis for substrate recruitment by AMBRA1 E3 ligase receptor

M. Liu, Y. Wang, F. Teng, X. Mai, W. Xi, M.-Y. Su, G. Stjepanovic

This study determines the cryo-EM structure of AMBRA1 bound to DDB1, revealing how AMBRA1 recruits substrates for ubiquitination and its role in autophagy and cell-cycle regulation.

bioRxiv · Dec 4, 2022 · PreprintBiochemistry

Monomethyl branched-chain fatty acid mediates amino acid sensing by mTORC1

M. ZHU, F. Teng, N. Li, L. Zhang, J. Shao, H. Sun, h. ZHU

This study identifies a leucine-derived fatty acid and glycosphingolipid that mediate amino acid sensing by mTORC1 in C. elegans, regulating development through protein translation and ribosomal biogenesis.

bioRxiv · Nov 30, 2020Cell Biology

Longitudinal multi-omics along gingivitis development reveal a suboptimal-health gum state with periodontitis-like microbiome

S. Huang, T. He, F. Yue, V. Xu, S. Wang, P. Zhu, F. Teng, Z. Sun, X. Liu, G. Jing, X. Su, L. Jin, J. Liu, J. Xu

The paper identifies a suboptimal-health gum state (SoH) during experimental gingivitis, characterized by microbiome and metabolite changes similar to periodontitis.

bioRxiv · Sep 26, 2020 · PreprintMicrobiology

Micro-XRF study of the troodontid dinosaur Jianianhualong tengi reveals new biological and taphonomical signals

J. Li, R. Pei, F. Teng, H. Qiu, R. Tagle, Q. Yan, Q. Wang, X. Chu, X. Xu

This study uses micro-XRF to analyze the holotype of Jianianhualong tengi, revealing elemental patterns linked to fossil structure and taphonomy.

bioRxiv · Sep 7, 2020Paleontology

SARS-CoV-2 proteome microarray for mapping COVID-19 antibody interactions at amino acid resolution

H. Wang, X. Hou, X. Wu, T. Liang, X. Zhang, D. Wang, F. Teng, J. Dai, H. Duan, S. Guo, Y. Li, X. Yu

This paper develops a SARS-CoV-2 proteome microarray to analyze antibody interactions at amino acid resolution and identifies epitopes and neutralizing antibodies in COVID-19 patients.

bioRxiv · Mar 26, 2020Biochemistry