Author

K. T. Nguyen

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· 3 Bioengineering· 2 Microbiology· 2 Cancer Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 7 Research Focus:cell type annotation· 6 Research Focus:cell signaling & trafficking· 3 Research Focus:protein folding & dynamics· 3 Assay:imaging· 2 Assay:proteomics· 2 Organism:bacteria (other)· 1 Approach:biophysical modeling· 1

Frequent Co-Authors

E. Villa· 3 shared J. Pogliano· 3 shared E. Armbruster· 2 shared E. Enustun· 2 shared J. Lee· 2 shared K. Khanna· 2 shared V. Chaikeeratisak· 2 shared A. B. Estelle· 1 shared

Activity by Year

2020-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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3 shared papersMicrobiology

E. Villa

Mutual co-authors in cluster

Author profile →

8 papers

Recent·Most cited

Limiting Brownian Motion to Enhance Immunogold Phenotyping and Superimpose Optical and Non-Optical Single-EP Analyses

K. T. Nguyen, X. Y. Rima, C. L. Hisey, J. Doon-Ralls, C. K. Nagaraj, E. Reategui

The paper introduces a technique to combine optical and non-optical single-EP analyses by limiting Brownian motion, enhancing immunogold phenotyping and enabling orthogonal measurements.

bioRxiv · Feb 22, 2024 · PreprintBioengineering

The OSUMMER lines: a series of ultraviolet-accelerated NRAS-mutant mouse melanoma cell lines syngeneic to C57BL/6

B. M. Murphy, D. M. Jensen, T. E. Arnold, R. Aguilar Valenzuela, J. Hughes, V. Posada, K. T. Nguyen, V. T. Chu, K. Y. Tsai, C. J. Burd, C. E. Burd

The paper introduces a series of NRAS-mutant melanoma cell lines derived from UV-exposed mice to model human melanoma resistance and therapy responses.

Pigment Cell & Melanoma Research · Sep 1, 2023Peer-reviewedCancer Biology

Identification of the bacteriophage nucleus protein interaction network

E. Enustun, A. Deep, Y. Gu, K. T. Nguyen, V. Chaikeeratisak, E. Armbruster, M. Ghassemian, E. Villa, J. Pogliano, K. D. Corbett

The paper identifies proteins interacting with the phage nucleus protein ChmA and describes their potential roles in genome packaging and transport.

bioRxiv · May 18, 2023Biochemistry

An auto-release mechanism for HMCES-DNA-protein crosslinks

M. Donsbach, S. Dürauer, K. T. Nguyen, F. Grünert, D. Yaneva, D. Semlow, J. Stingele

This study identifies a non-proteolytic release mechanism for HMCES-DNA-protein crosslinks regulated by DNA context, enabling efficient repair by APE1.

bioRxiv · Dec 18, 2022Biochemistry

Genetic encoding of 3-nitro-tyrosine reveals the impacts of 14-3-3 nitration on client binding and dephosphorylation

P. Zhu, K. T. Nguyen, A. B. Estelle, N. N. Sluchanko, R. A. Mehl, R. B. Cooley

This study genetically encodes 3-nitro-tyrosine in 14-3-3 proteins to investigate how nitration at Y130 and Y213 affects structure, function, and client binding.

bioRxiv · Nov 11, 2022Biochemistry

Subcellular Organization of Viral Particles During Maturation of Nucleus-Forming Jumbo Phage

V. Chaikeeratisak, K. Khanna, K. T. Nguyen, M. E. Egan, E. Enustun, E. Armbruster, K. Pogliano, E. Villa, J. Pogliano

The paper visualizes the subcellular organization of mature viral particles in nucleus-forming jumbo phages, revealing a structured assembly process called phage bouquets.

bioRxiv · Apr 26, 2021Microbiology

Notch Intracellular Domain Plasmid Delivery via Poly(lactic-co-glycolic acid)Nanoparticles to Upregulate Notch Signaling

V. Messerschmidt, A. Kuriakose, U. Chintapula, S. Laboy-Segarra, T. Truong, L. A. Kydd, J. Jaworski, K. T. Nguyen, J. Lee

This study delivers Notch Intracellular Domain plasmid via PLGA nanoparticles to upregulate Notch signaling in HUVECs, showing nontoxicity, stability, and successful gene expression.

bioRxiv · Apr 16, 2021Bioengineering

Selective transport of fluorescent proteins into the phage nucleus

K. T. Nguyen, J. Sugie, K. Khanna, E. E. MacKennon, E. A. Birkholz, J. Lee, C. Beierschmitt, E. Villa, J. Pogliano

The paper investigates nuclear transport in phage infection systems, finding that GFPmut1 can be selectively transported into the {Phi}KZ phage nucleus, with specific amino acid residues identified for this process.

bioRxiv · Nov 25, 2020Microbiology