Author

K. Matoba

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· 1 Bioengineering· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:host-pathogen & immune response· 2 Organism:mouse· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Organism:human· 1

Frequent Co-Authors

N. N. Noda· 2 shared C. Kabuta· 1 shared D. Bolidong· 1 shared D. Hishikawa· 1 shared F. Hamano· 1 shared G. Matsumoto· 1 shared H. Fujita· 1 shared H. Kikuchi· 1 shared

Activity by Year

2020-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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2 shared papersBiochemistry

N. N. Noda

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Surface-engineered extracellular vesicles to modulate antigen-specific T cell expansion for cancer immunotherapy

X. Lyu, T. Yamano, S. Imai, T. V. Le, D. Bolidong, M. Ueda, S. Warashina, H. Mukai, S. Hayashi, K. Matoba, T. Nishino, R. Hanayama

The paper develops antigen-presenting extracellular vesicles (AP-EVs) engineered to enhance T cell expansion and anticancer immunity through combined immunotherapy.

bioRxiv · Sep 25, 2023 · PreprintBioengineering

Mutagenesis and homology modeling reveal a predicted pocket of lysophosphatidylcholine acyltransferase 2 to catch Acyl-CoA.

F. Hamano, K. Matoba, T. Hashidate, T. Suzuki, K. Miura, D. Hishikawa, T. Harayama, K. Yuki, Y. Kita, N. N. Noda, T. Shimizu, H. Shindou

The paper identifies key residues and an acyl-CoA-binding pocket in mouse LPCAT2 using homology modeling, providing structural insights for drug development against PAF-related diseases.

bioRxiv · Oct 31, 2020Biochemistry

Lysosomal microautophagic pathway links proteostasis to protein aggregation disease

Y. Fujiwara, C. Kabuta, V. R. Contu, M. Ogawa, H. Fujita, H. Kikuchi, R. Sakai, M. Suzuki, I. Koyama-Honda, M. Inoue, Y. Oya, Y. U. Inoue, T. Inoue, R. Takahashi, G. Matsumoto, , T. Kabuta

This study identifies SIDT2 as a mediator of microautophagy that delivers cytosolic proteins into lysosomes, linking proteostasis to protein aggregation disease.

bioRxiv · Aug 11, 2020 · PreprintCell Biology