Author

E. D'Este

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Biochemistry· 3 Biophysics· 2 Cell Biology· 2 Physiology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 6 Assay:fluorescence / live-cell microscopy· 6 Research Focus:cell type annotation· 4 Organism:human· 3 Research Focus:imputation· 3 Organism:mouse· 3 Assay:imaging· 2 Research Focus:spatial domain detection· 2

Frequent Co-Authors

K. Johnsson· 3 shared J. Ast· 2 shared J. Broichhagen· 2 shared S. W. Hell· 2 shared A. Arvaniti· 1 shared A. Bacon· 1 shared A. Hüper· 1 shared A. K. Linnemann· 1 shared

Activity by Year

2019-2022 · peak 4/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

3 shared papersCell Biology

K. Johnsson

Mutual co-authors in cluster

Author profile →

8 papers

Recent·Most cited

Exchangeable HaloTag Ligands (xHTLs) for multi-modal super-resolution fluorescence microscopy

J. Kompa, J. Bruins, M. Glogger, J. Wilhelm, M. S. Frei, M. Tarnawski, E. d'Este, M. Heilemann, J. Hiblot, K. Johnsson

The paper introduces exchangeable HaloTag ligands for multi-modal super-resolution fluorescence microscopy, enabling dual-color imaging techniques like PAINT and STED.

bioRxiv · Jun 20, 2022 · PreprintBiochemistry

A general design of caging-group free photoactivatable fluorophores for live-cell nanoscopy

R. Lincoln, M. L. Bossi, M. Remmel, E. D'Este, A. N. Butkevich, S. W. Hell

This paper introduces a method to create caging-group free photoactivatable fluorophores for live-cell nanoscopy, demonstrating their utility in multiple superresolution techniques.

bioRxiv · Nov 15, 2021Biochemistry

Optimal Precision and Accuracy in 4Pi-STORM using Dynamic Spline PSF Models

M. Bates, J. Keller-Findeisen, A. Przybylski, A. Hüper, T. Stephan, P. Ilgen, A. R. Cereceda Delgado, E. D'Este, S. Jakobs, S. J. Sahl, S. W. Hell

This paper develops a 4Pi-STORM microscope with dynamic spline PSF models to achieve high 3D resolution and accuracy in single molecule localization microscopy.

bioRxiv · Oct 19, 2021Biophysics

Systematic Tuning of Rhodamine Spirocyclization for Super-Resolution Microscopy

N. Lardon, L. Wang, A. Tschanz, P. Hoess, M. Tran, E. D'Este, J. Ries, K. Johnsson

This paper describes a method to systematically tune the spirocyclization equilibrium of rhodamines to create probes for different super-resolution microscopy techniques.

bioRxiv · May 20, 2021Cell Biology

Actin in Dendritic Spines Self-Organizes into a Critical State

M. Bonilla-Quintana, F. Woergoetter, E. D'Este, C. Tetzlaff, M. Fauth

The paper quantifies dendritic spine size and shape changes using time-series analysis and proposes a biophysical model showing actin self-organization into a critical state.

Scientific Reports · Feb 17, 2021Peer-reviewedBiophysics

Overcoming efflux of fluorescent probes for actin imaging in living cells

R. Gerasimaite, J. Seikowski, J. Schimpfhauser, G. Kostiuk, T. Gilat, E. D'Este, S. Schnorrenberg, G. Lukinavicius

The paper develops fluorescent actin probes that overcome efflux by plasma membrane pumps, enabling effective staining in multiple organisms and cell types without inhibitors.

bioRxiv · Feb 17, 2020 · PreprintBiochemistry

Interrogating surface versus intracellular transmembrane receptor populations using cell-impermeable SNAP-tag substrates

P. Poc, V. A. Gutzeit, J. Ast, J. Lee, B. Jones, E. D'Este, B. Mathes, D. Hodson, J. Levitz, J. Broichhagen

The paper introduces SBG-conjugated fluorophores to improve extracellular labeling of SNAP-fused proteins, enabling precise analysis of GPCR populations in living cells and tissues.

bioRxiv · Jan 29, 2020Physiology

LUXendins reveal endogenous glucagon-like peptide-1 receptor distribution and dynamics

J. Ast, A. Arvaniti, N. H. F. Fine, D. Nasteska, F. B. Ashford, Z. Stamataki, Z. Koszegi, A. Bacon, S. Trapp, B. J. Jones, B. Hastoy, A. Tomas, C. Reissaus, A. K. Linnemann, E. D'Este, , D. J. Hodson

The paper introduces LUXendin peptides that label and visualize endogenous GLP1R with high specificity, revealing receptor organization and dynamics.

bioRxiv · May 8, 2019Cell Biology