Author

Kentaro Iso

University of DundeeORCID 0000-0001-5417-3642Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Approach:biophysical modeling· 1 Approach:deep learning· 1 Research Focus:drug response / drug discovery· 1 Organism:human· 1 Research Focus:protein folding & dynamics· 1 Assay:protein structure· 1 Assay:proteomics· 1

Frequent Co-Authors

Alessio CiulliiD· 2 shared Gajanan J. SatheiD· 2 shared Mark A. NakasoneiD· 2 shared Aitana de la Cuadra BastéiD· 1 shared Alejandro Correa-SáeziD· 1 shared Angus D. CowaniD· 1 shared Carlo J. A. VerhoefiD· 1 shared Caroline SchätziD· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersBiochemistry

Alessio CiulliORCID

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2 papers

Recent·Most cited

BiochemistrybioRxivPreprintNov 17, 2025

Induced ubiquitination of the partially disordered Estrogen Receptor alpha protein via a 14-3-3-directed molecular glue-based PROTAC design

Carlo J. A. Verhoef, Charlotte Crowe, Mark A. Nakasone…·Peter J. Cossar

This paper develops a molecular glue-based PROTAC (MGPROTACs) to ubiquitinate the 14-3-3/Estrogen Receptor complex, demonstrating cooperative complex formation and selective ubiquitination through linker design.

DOI 10.1101/2025.11.17.688825

protein structuredeep learning

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BiochemistrybioRxivPreprintAug 4, 2025

Dual E3 ligase recruitment by monovalent degraders enables redundant and tuneable degradation of SMARCA2/4

Valentina A. Spiteri, Dmitri Segal, Alejandro Correa-Sáez…·Georg E. Winter

This study shows that a monovalent MGD can recruit two E3 ligases redundantly to degrade SMARCA2/4, with tunable ligase preference through chemical and genetic modifications.

7 citations

humanproteomics

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