Author

Masanori Mishima

University of WarwickORCID 0000-0002-8908-7485Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Biochemistry· 1 Bioengineering· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:development & morphogenesis· 1 Assay:fluorescence / live-cell microscopy· 1 Approach:genetic perturbation / CRISPR· 1 Research Focus:protein design· 1 Assay:structural biology· 1

Frequent Co-Authors

Mohan K. BalasubramanianiD· 2 shared Abhishek KumariD· 1 shared Allister CrowiD· 1 shared Andrejus SuchenkoiD· 1 shared Benjamin Heath DurhamiD· 1 shared Clyde Savio PintoiD· 1 shared Dipayan AkhuliiD· 1 shared Esther Ivorra-MollaiD· 1 shared

Activity by Year

2021-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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2 shared papersBiochemistry

Mohan K. BalasubramanianORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

Structure and physiological investigation of arginylated actin

Clyde Savio Pinto, Saskia E. Bakker, Andrejus Suchenko, Isabella M. Kolodny, Hamdi Hussain, Tomoyuki Hatano, Karuna Sampath, Krishna Chinthalapudi, Sarah M. Heissler, Masanori Mishima, Mohan K. Balasubramanian

This study investigates the structure and function of arginylated beta-actin, showing structural similarity to non-arginylated actin but altered interactions with myosin-II and effects on cellular processes.

The Journal of Cell Biology · Nov 14, 2025Peer-reviewedBiochemistry

StayRose: a photostable StayGold derivative red-shifted by genetic code expansion

William Scott, Esther Ivorra-Molla, Dipayan Akhuli, Teresa Massam-Wu, Pawel K Lysyganicz, Rylie Walsh, Matthew T. Parent, Jonathan Cook, Lijiang Song, Abhishek Kumar, Falk Schneider, Masanori Mishima, Allister Crow, Mohan K. Balasubramanian

The paper describes the creation of StayRose, a red-shifted variant of StayGold using genetic code expansion, which retains photostability and can be monomerised.

Journal of Biological Chemistry · Oct 17, 2025Peer-reviewedBioengineering

A rare congenital anemia is caused by mutations in the centralspindlin complex

Sandeep N. Wontakal, Mishan Britto, Sarah Tannenbaum, Benjamin Heath Durham, Margaret T. Lee, Masanori Mishima

This study identifies compound heterozygous RACGAP1 variants causing CDAIII by disrupting the centralspindlin complex, leading to cytokinesis defects.

medRxiv · Apr 7, 2021 · PreprintGenetic & Genomic Medicine