Author

G. Xue

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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Cell Biology· 2 Biochemistry· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Research Focus:cell signaling & trafficking· 2 Research Focus:host-pathogen & immune response· 2 Organism:human· 2 Assay:proteomics· 2 Approach:biophysical modeling· 1 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1

Frequent Co-Authors

A. Machado de Amorim· 1 shared A. T. Gres· 1 shared B. K. Ganser-Pornillos· 1 shared C. J. Mann· 1 shared C.-K. Kwok· 1 shared D. Goncalves-Carneiro· 1 shared D. M. Dawidziak· 1 shared D. Wang· 1 shared

Activity by Year

2020-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 10 mutual co-author links

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1 shared paperBiochemistry

A. Machado de Amorim

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4 papers

Recent·Most cited

Modulation of RNA binding properties of the RNA helicase UPF1 by its activator UPF2

G. Xue, V. D. Maciej, A. Machado de Amorim, M. Pak, U. Jayachandran, S. Chakrabarti

This study shows that UPF2 binding reduces UPF1's RNA affinity, causing RNA release through an allosteric effect rather than direct competition.

bioRxiv · Mar 26, 2022Biochemistry

The HIV-1 capsid core is an opportunistic nuclear import receptor

G. Xue, H. J. Yu, S. L. Goh, A. T. Gres, M. H. Guney, S. G. Sarafianos, J. Luban, V. N. KewalRamani

This study identifies HIV-1 capsid proteins as a nuclear import receptor that interacts with host nucleoporins and soluble factors to facilitate nuclear entry.

bioRxiv · Dec 2, 2021Cell Biology

Poly(ADP-ribose) potentiates ZAP antiviral activity

O. Pornillos, G. Xue, K. Braczyk, D. Goncalves-Carneiro, H. Ong, D. M. Dawidziak, K. Zawada, W. Yueping, K. K. Zadrozny, B. K. Ganser-Pornillos, P. D. Bieniasz

This study shows that poly(ADP-ribose) enhances ZAP's ability to degrade viral RNA by binding to ZAP's WWE domains, improving its antiviral activity against HIV-1.

bioRxiv · Dec 17, 2020Microbiology

mRNA translation control by Dhx36 binding to 5' UTR G-quadruplex structures is essential for skeletal muscle stem cell regenerative functions

X. Chen, J. Yuan, G. Xue, S. Campanario Sanz, D. Wang, W. Wang, X. Mou, M. I. I. Umar, J. Isern, Y. Zhao, L. He, Y. Li, C. J. Mann, X. Yu, L. Wang, , H. Wang

This study identifies Dhx36 as essential for skeletal muscle stem cell regeneration by regulating mRNA translation through binding and unwinding 5' UTR G-quadruplex structures.

bioRxiv · Aug 30, 2020Cell Biology