Author

M. Postma

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· 6 Scientific Communication & Education· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

J. Goedhart· 7 shared T. W. J. Gadella· 5 shared A. O. Chertkova· 3 shared E. K. Mahlandt· 2 shared J. D. van Buul· 2 shared J. J. G. Arts· 2 shared M. Mastop· 2 shared S. van der Niet· 2 shared

Activity by Year

2016-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 32 mutual co-author links

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7 shared papersCell Biology

J. Goedhart

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Author profile →

7 papers

Recent·Most cited

A turquoise fluorescence lifetime-based biosensor for quantitative imaging of intracellular calcium

F. H. van der Linden, E. K. Mahlandt, J. J. G. Arts, J. Beumer, J. Puschhof, S. M. A. de Man, A. O. Chertkova, B. Ponsioen, H. Clevers, J. D. van Buul, M. Postma, T. W. J. Gadella, J. Goedhart

This paper introduces a new calcium biosensor based on fluorescence lifetime imaging, which provides accurate and pH-insensitive quantification of intracellular calcium concentrations.

bioRxiv · Jun 21, 2021Cell Biology

Endothelial junctional membrane protrusions serve as hotspots for neutrophil transmigration

J. J. G. Arts, E. K. Mahlandt, M. Grönloh, L. Schimmel, I. Noordstra, A. C. I. van Steen, S. Tol, J. van Rijssel, M. A. Nolte, M. Postma, S. Khuon, J. M. Heddleston, E. Wait, T. L. Chew, M. Winter, , J. D. van Buul

The paper identifies endothelial junctional membrane protrusions as preferred sites for neutrophil transmigration during inflammation and shows they depend on Rac1 activity.

bioRxiv · Jan 18, 2021Cell Biology

Robust and Bright Genetically Encoded Fluorescent Markers for Highlighting Structures and Compartments in Mammalian Cells

A. O. Chertkova, M. Mastop, M. Postma, N. van Bommel, S. van der Niet, K. L. Batenburg, L. Joosen, T. W. J. Gadella, Y. Okada, J. Goedhart

bioRxiv · Jan 13, 2020 · PreprintCell Biology

Selectivity of Guanine Nucleotide Exchange Factor-mediated Cdc42 activation in primary human endothelial cells

N. R. Reinhard, S. van der Niet, A. O. Chertkova, M. Postma, P. L. Hordijk, T. W. J. Gadella, J. Goedhart

The paper quantifies Cdc42 activation by endothelial GEFs in primary human cells, identifying FGD1 as the most selective activator.

bioRxiv · Feb 5, 2019Cell Biology

PlotsOfData - a web app for visualizing data together with its summaries

M. Postma, J. Goedhart

PlotsOfData is a web app that visualizes raw data with statistical summaries using ggplot2, offering flexibility in data display and interpretation.

bioRxiv · Nov 13, 2018Scientific Communication & Education

Characterization of a spectrally diverse set of fluorescent proteins as FRET acceptors for mTurquoise2

M. Mastop, D. S. Bindels, N. C. Shaner, M. Postma, T. W. J. Gadella, J. Goedhart

The paper evaluates fluorescent proteins as FRET acceptors for mTurquoise2, identifying mNeonGreen as the most efficient and photostable pair.

bioRxiv · Jun 27, 2017Cell Biology

Palmitoylation of the oncogenic RhoGEF TGAT is dispensable for membrane localization and consequent activation of RhoA

J. van Unen, D. Botman, T. Yin, Y. I. Wu, M. A. Hink, T. W. J. Gadella, M. Postma, J. Goedhart

This study shows that membrane association of TGAT is critical for its activity, but palmitoylation is not required for membrane localization or RhoA activation.

bioRxiv · Aug 9, 2016Cell Biology