Author

J. H. Ipsen

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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Biophysics· 4 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Approach:statistical model· 2 Research Focus:cell signaling & trafficking· 1 Approach:deep learning· 1 Organism:human· 1 Assay:imaging· 1 Approach:simulation· 1 Research Focus:software / tool· 1

Frequent Co-Authors

J. C. Shillcock· 3 shared W. Pezeshkian· 2 shared A. D. Brown· 1 shared A. Darbyson· 1 shared C. Lagisquet· 1 shared D. A. Ford· 1 shared D. Thomas· 1 shared E. Chenais· 1 shared

Activity by Year

2017-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 15 mutual co-author links

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3 shared papersBiophysics

J. C. Shillcock

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Author profile →

5 papers

Recent·Most cited

Mesoscale simulation of biomembranes with FreeDTS

W. Pezeshkian, J. H. Ipsen

The paper introduces FreeDTS, a software for mesoscale biomembrane simulation, allowing realistic membrane shape modeling and protein organization analysis.

bioRxiv · May 5, 2023Biophysics

Macromolecular crowding is surprisingly unable to deform the structure of a model biomolecular condensate

J. C. Shillcock, D. Thomas, J. H. Ipsen, A. D. Brown

This study investigates how macromolecular crowding affects model biomolecular condensates, finding that crowding agents do not significantly alter their structure.

bioRxiv · Dec 12, 2022Biophysics

Model biomolecular condensates have heterogeneous structure quantitatively dependent on the interaction profile of their constituent macromolecules

J. C. Shillcock, C. Lagisquet, J. Alexandre, L. Vuillon, J. H. Ipsen

The paper uses simulations to show that model intrinsically-disordered proteins form heterogeneous, structured condensates whose properties depend on binding site arrangement and affinity.

bioRxiv · Mar 25, 2022Biophysics

Structure of Biomolecular Condensates from Dissipative Particle Dynamics Simulations

J. C. Shillcock, M. Brochut, E. Chenais, J. H. Ipsen

This study uses simulations to investigate the structure and phase behavior of biomolecular condensates formed by semi-flexible polymers with end-caps, revealing how their properties depend on molecular features.

bioRxiv · Dec 11, 2019 · PreprintBiophysics

C24 sphingolipids play a surprising and central role in governing cholesterol and lateral organization of the live cell plasma membrane

K. C. Courtney, W. Pezeshkian, R. Raghupathy, G. Zhang, A. Darbyson, J. H. Ipsen, D. A. Ford, H. Khandelia, J. F. Presley, X. Zha

This study shows that C24 sphingomyelin in the outer leaflet suppresses membrane microdomains by directing cholesterol to the inner leaflet, while C16 sphingomyelin promotes microdomains.

bioRxiv · Oct 31, 2017Cell Biology