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Ana J. García-Sáez

Researcher at University of Cologne

Publications -  131
Citations -  10109

Ana J. García-Sáez is an academic researcher from University of Cologne. The author has contributed to research in topics: Membrane & Vesicle. The author has an hindex of 37, co-authored 115 publications receiving 6333 citations. Previous affiliations of Ana J. García-Sáez include Max Planck Society & University of Tübingen.

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Journal ArticleDOI

Scanning Fluorescence Correlation Spectroscopy for Quantification of the Dynamics and Interactions in Tube Organelles of Living Cells

TL;DR: Tube scanning fluorescence cross-correlation spectroscopy is introduced for the absolute quantification of diffusion and complex formation of fluorescently labeled molecules in the mitochondrial compartments and it is discovered that practically all mitochondria-bound Bcl-xL and tBid are associated with each other, in contrast to undetectable association in the cytosol.
Book ChapterDOI

AFM to Study Pore-Forming Proteins.

TL;DR: Rugby protocols to investigate the effect of pore-forming proteins in supported lipid bilayers are described and both the structural reorganization of the membrane surface and the changes in the force required for membrane piercing upon incubation with this special type of proteins are described.
Book ChapterDOI

Scanning Fluorescence Correlation Spectroscopy in Model Membrane Systems

TL;DR: The theoretical basis of point FCS as well as the scanning FCS (SFCS) approach are described, which is a practical way to address the challenges of FCS with membranes.
Journal ArticleDOI

Necroptosis Execution is Mediated by Plasma Membrane Nanopores that are Independent of Calcium

TL;DR: The findings reconcile apparent contradictions about the essential role of different ions in necroptosis taking into account that different ions could pass through punched membranes, and demonstrate that early calcium influx does not modulate the size of the later pores formed in the plasma membrane.
Journal ArticleDOI

Early activation of CD95 is limited and localized to the cytotoxic synapse.

TL;DR: An artificial cytotoxic synapse is developed to examine how mobility and geometry of an anti‐CD95 agonistic antibody affect receptor aggregation and mobility, ie the first step of receptor activation.