Author

T. Yoshimori

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· 3

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:cell signaling & trafficking· 2 Assay:proteomics· 2 Research Focus:cell type annotation· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Organism:yeast· 1

Frequent Co-Authors

M. Hamasaki· 2 shared A. C. Hernandez· 1 shared A. G. Duran· 1 shared A. Kuma· 1 shared A. Nezu· 1 shared C. Belmonte-Mateos· 1 shared D. P. Farrell· 1 shared E. Adachi-Fernandez· 1 shared

Activity by Year

2020-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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2 shared papersCell Biology

M. Hamasaki

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Author profile →

3 papers

Recent·Most cited

Golgi membrane proteins YIPF3 and YIPF4 regulate turnover of the Golgi apparatus through autophagy

S. Kitta, T. Kaminishi, M. Higashi, T. Shima, H. Kosako, T. Yoshimori, A. Kuma

This study identifies YIPF3 and YIPF4 as Golgi-specific autophagy receptors that mediate Golgi turnover via selective autophagy.

bioRxiv · Aug 9, 2023 · PreprintCell Biology

Drs2 regulates TRAPPIII in Atg9 transport: exposing the interplay of P4-ATPases and Multisubunit Tethering Complexes

I. Pazos, M. Puig-Tinto, J. Cordero, N. Jimenez-Menendez, M. Abella, A. G. Duran, E. Adachi-Fernandez, C. Belmonte-Mateos, S. Sabido-Bozo, A. C. Hernandez, S. Tosi, A. Nezu, J. Colombelli, T. R. Graham, T. Yoshimori, , O. Gallego

The paper investigates how Drs2 interacts with TRAPPIII to regulate Atg9 transport during selective autophagy, revealing a novel role for P4-ATPases in this process.

bioRxiv · Dec 25, 2020Cell Biology

Structural basis for autophagy inhibition by the human Rubicon-Rab7 complex

H. K. Bhargava, K. Tabata, J. K. Byck, M. Hamasaki, D. P. Farrell, I. Anishchenko, F. DiMaio, Y.-J. Im, T. Yoshimori, J. H. Hurley

This study determines the crystal structure of the Rubicon RH domain bound to Rab7-GTP, revealing its mechanism of autophagy inhibition and validating it as a therapeutic target.

bioRxiv · Apr 18, 2020Cell Biology