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Biology subjects

Franziscus, C. A.

Publications and source records attributed to Franziscus, C. A..

2 recordsLinked to original sources

SPEx: Compartment-Resolved Proteomics via Expansion Microscopy-Guided Microdissection

Cells contain different organelles and compartments that are essential for cellular function and life. These organelles and compartments need to communicate to assess cellular state in a changing environment, adapt to the new situation, and also to ensure functionality and homeostasis. Moreover, organization and communication differ between cell types. However, our knowledge about these changes is still rather scarce. Subcellular spatial proteomics aims to fill this knowledge gap. While proximity labeling techniques represent a great advance, they do not provide precise spatial resolution. To overcome this limitation, we developed SPEx (Subcellular spatial Proteomics coupled to Expansion), in which we first expand cells about 10- fold, laser micro-dissect regions of interests and then perform mass spectrometry-based proteomics on these samples. We demonstrate the effectiveness of SPEx by determining the proteome of the Golgi, the nucleus and nucleoli. Satisfyingly, we also identify novel components of these organelles. Combining inexpensive already existing technologies makes SPEx readily usable by the wider scientific community.

cell biology↗

ARF-1 Coordinates Cargo Sorting at FERARI Endosomal Recycling Hubs

Endosomal pathways are central to cellular organization, compartmentalization, and intercellular communication. Independent of the endocytic entry route, sorting endosomes function as critical junctions at which membrane proteins are sorted for recycling or degradation. The multicomponent tether FERARI orchestrates recycling by coordinating Rab GTPase activity with vesicle fusion and fission through a kiss-and-run mechanism. Here, we identify the small GTPase ARF-1 as an essential regulator of cargo loading at FERARI-dependent endosomal kiss-and-run (KAR) sites. Cycling of ARF-1 between its active and inactive states is required for efficient cargo capture into recycling vesicles. Our findings support a model in which cycling ARF-1 activity governs the temporal association of cargo with adaptor proteins and complexes, thereby controlling selective uptake into vesicles destined for the plasma membrane. These results uncover a previously unappreciated layer of regulation of endosomal recycling and highlight the interplay between ARF and Rab family GTPases in this process.

cell biology↗