Author

J. Schoeneberg

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· 5 Biophysics· 1 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 5 Approach:experimental assay· 4 Organism:human· 3 Research Focus:cell type annotation· 2 Approach:deep learning· 2 Assay:fluorescence / live-cell microscopy· 2 Assay:imaging· 2 Approach:microscopy & imaging analysis· 2

Frequent Co-Authors

D. G. Drubin· 3 shared C. Kaplan· 2 shared H. Hakozaki· 2 shared K. Xu· 2 shared M. Akamatsu· 2 shared P. Natekar· 2 shared S. Chen· 2 shared Z. Wang· 2 shared

Activity by Year

2018-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

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3 shared papersCell Biology

D. G. Drubin

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Author profile →

7 papers

Recent·Most cited

Self-supervised deep learning uncovers the semantic landscape of drug-induced latent mitochondrial phenotypes

P. Natekar, Z. Wang, M. Arora, H. Hakozaki, J. Schoeneberg

This study introduces MitoSpace, a self-supervised deep learning approach to map drug-induced mitochondrial phenotypes, revealing a more complex morphology landscape than previously thought.

bioRxiv · Sep 13, 2023 · PreprintPharmacology & Toxicology

MitoTNT: Mitochondrial Temporal Network Tracking for 4D live-cell fluorescence microscopy data

Z. Wang, P. Natekar, C. Tea, S. Tamir, H. Hakozaki, J. Schoeneberg

MitoTNT tracks mitochondrial networks in 4D live-cell imaging data, revealing movement patterns and dynamic responses to pharmacological treatments.

bioRxiv · Aug 16, 2022 · PreprintCell Biology

Actin force generation in vesicle formation: mechanistic insights from cryo-electron tomography

D. Serwas, M. Akamatsu, A. Moayed, K. Vegesna, R. Vasan, J. M. Hill, J. Schoeneberg, K. M. Davies, P. Rangamani, D. G. Drubin

The paper uses cryo-electron tomography to study actin filament organization during clathrin-mediated endocytosis, revealing how actin dynamics generate pulling forces for vesicle formation.

bioRxiv · Jun 28, 2021Cell Biology

Xist-seeded nucleation sites form local concentration gradients of silencing proteins to inactivate the X-chromosome

Y. Markaki, J. G. Chong, C. Luong, S. Y. X. Tan, Y. Wang, E. C. Jacobson, D. Maestrini, I. Dror, B. A. Mistry, J. Schoeneberg, A. Banerjee, M. Guttman, T. Chou, K. Plath

This study identifies Xist-seeded nucleation sites that create local concentration gradients of silencing proteins, leading to X-chromosome inactivation through macromolecular crowding.

bioRxiv · Nov 22, 2020Cell Biology

Load adaptation of endocytic actin networks

C. Kaplan, S. J. Kenny, S. Chen, J. Schoeneberg, E. Sitarska, A. Diz-Munoz, M. Akamatsu, K. Xu, D. G. Drubin

The paper investigates how actin networks adapt to membrane tension during clathrin-mediated endocytosis, finding that actin assembly increases under elevated load to maintain CME robustness.

bioRxiv · Apr 5, 2020 · PreprintCell Biology

Direct comparison of clathrin-mediated endocytosis in budding and fission yeast reveals conserved and evolvable features

Y. Sun, J. Schoeneberg, S. Chen, T. Jiang, C. Kaplan, K. Xu, T. Pollard, D. G. Drubin

This study compares clathrin-mediated endocytosis in budding and fission yeast, finding conserved mechanisms and species-specific adaptations in actin assembly and membrane invagination.

bioRxiv · Aug 13, 2019Cell Biology

ATP-dependent force generation and membrane scission by ESCRT-III and Vps4

J. Schoeneberg, S. Yan, M. Righini, M. Remec Pavlin, I.-H. Lee, L.-A. Carlson, A. H. Bahrami, D. H. Goldman, X. Ren, G. Hummer, C. Bustamante, J. Hurley

ESCRT-III and Vps4 were reconstituted to generate ATP-dependent forces for membrane scission, confirming their role in membrane cutting.

bioRxiv · Feb 7, 2018Biophysics