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Biology subjects

Matthias, G.

Publications and source records attributed to Matthias, G..

3 recordsLinked to original sources

Dynamic profiling of the aggresome processing pathway

Cellular homeostasis is maintained by the efficient degradation of proteins by the 26S proteasome, a key component of the ubiquitin proteasome system. When the proteasome function is impaired due to cellular stress like mutations, chemicals or epigenetic stressors, there is accumulation of unfolded or misfolded, ubiquitinated proteins leading to cellular toxicity. Cells combat this rise in cellular toxicity by sequestering ubiquinated proteins in a transient cellular structure called the aggresome. The transport of this ubquitinated protein cargo along the microtubules to form aggresomes and their clearance from cells by autophagy is called the aggresome processing pathway (APP). APP activation is a hallmark of several neurodegenerative diseases and has also been implicated in Influenza A Virus uncoating step. To study the dynamics of APP and the compositional diversity of the aggresome, we used time-dependent proximity labeling, mass spectrometry, and immunofluorescence microscopy. Here, we used vimentin (VIM) and histone deacetylase 6 (HDAC6), two established aggresome markers as baits to visualize aggresome formation and clearance in HeLa cells. We identified more than 75 novel components of mature aggresome. Further, we characterised the time-dependent protein-protein interactions in the neighbourhood of VIM and HDAC6 during APP progression. Our study identified new interactors of VIM and HDAC6 that maybe involved in aggresome clearance by autophagy. Together, our findings uncover novel APP-associated proteins that are central to advancing the understanding of this poorly characterized and highly complex pathway implicated in multiple diseases.

molecular biology↗

Ubiquitination mediates protein localization in RNA virus-infected cells

Viruses trigger monocytes proinflammatory and antiviral responses. Ubiquitination, a post-translational modification primarily marking proteins for degradation, regulates cellular responses to virus infection. However, a comprehensive analysis of virus-induced ubiquitination in monocytes is lacking. Here we identified a widespread increase of ubiquitination under viral RNA challenge or influenza infection in monocytes. Systematic proteome studies revealed that influenza infection elicits dynamic ubiquitinome alterations, with a notable transition from early to late stage. Most of this increased ubiquitination is not proteolytic and targets proteins involved in subcellular localization, such as the mitochondrial protein COA7 which, when ubiquitinated during infection, translocates to the nucleus and inhibits stress granules formation and TNF- expression. Blocking ubiquitination halts viral ribonucleoproteins nuclear export, highlighting ubiquitinations importance for protein localization during virus infection.

molecular biology↗

A global screen for assembly state changes of the mitotic proteome by SEC-SWATH-MS

Living systems integrate biochemical reactions that determine the functional state of each cell. Reactions are primarily mediated by proteins that have in systematic studies been treated as independent entities, disregarding their higher level organization into complexes which affects their activity and/or function and is thus of great interest for biological research. Here, we describe the implementation of an integrated technique to quantify cell state-specific changes in the physical arrangement of protein complexes, concurrently for thousands of proteins and hundreds of complexes. Applying this technique for comparison of human cells in interphase and mitosis, we provide a systematic overview of mitotic proteome reorganization. The results recall key hallmarks of mitotic complex remodeling and discover new events, such as a new model of nuclear pore complex disassembly, validated by orthogonal methods. To support the interpretation of quantitative SEC-SWATH-MS datasets, we extend the software CCprofiler and provide an interactive exploration tool, SECexplorer-cc.\n\nHighlightsO_LIQuantification of proteome assembly state changes using SEC-SWATH-MS\nC_LIO_LISystems-wide analysis of assembly state changes in the mitotic proteome\nC_LIO_LIDiscovery and validation of a novel mitotic disassembly intermediate of the nuclear pore complex\nC_LIO_LIHigher sensitivity and information content compared to thermostability-based approaches for global measurement of proteome states\nC_LIO_LISECexplorer, an online platform to browse results and investigate proteins newly implicated in cell division\nC_LI

systems biology↗