scispace - formally typeset
M

Matthias Peter

Researcher at ETH Zurich

Publications -  202
Citations -  24583

Matthias Peter is an academic researcher from ETH Zurich. The author has contributed to research in topics: Ubiquitin ligase & Cullin. The author has an hindex of 75, co-authored 192 publications receiving 21916 citations. Previous affiliations of Matthias Peter include ISREC & Swiss Institute of Bioinformatics.

Papers
More filters
Journal ArticleDOI

The Clathrin Adaptor Gga2p Is a Phosphatidylinositol 4-phosphate Effector at the Golgi Exit

TL;DR: This analysis uncovered a PI(4)P-dependent recruitment of the clathrin adaptor Gga2p to the TGN during Golgi-to-endosome trafficking and provides an explanation for the T GN-specific membrane recruitment of GGA2p.
Journal ArticleDOI

An interaction network of the mammalian COP9 signalosome identifies Dda1 as a core subunit of multiple Cul4-based E3 ligases

TL;DR: This analysis identifies new components of the CRL family of E3 ligases and elaborates new connections between the C RL and CSN complexes, including Dda1, which is characterized as a chromatin-associated core subunit of multiple CRL4 proteins.
Journal ArticleDOI

A Dual Protein-mRNA Localization Screen Reveals Compartmentalized Translation and Widespread Co-translational RNA Targeting.

TL;DR: A dual protein-mRNA localization screen using smFISH on human cell lines expressing GFP-tagged genes revealed a high degree of intercellular heterogeneity, and translation factories uniquely regulate nascent protein metabolism and create a fine granular compartmentalization of translation.
Journal ArticleDOI

Yeast split-ubiquitin-based cytosolic screening system to detect interactions between transcriptionally active proteins

TL;DR: The cytosolic yeast two-hybrid system (cytoY2H) is presented, which is based on the split-ubiquitin technique and detects protein-protein interactions in the cytoplasm and applied to cDNA library screening and identified several new interaction partners of Uri1p, an uncharacterized yeast protein.
Journal ArticleDOI

Modular microfluidics enables kinetic insight from time-resolved cryo-EM

TL;DR: A time-resolved sample preparation method for cryo-EM called trEM is presented, which uses a microfluidic device to initiate the biochemical reaction by rapid mixing of the components and then spraying the sample onto a cryO-EM grid to snap-freeze it in a blot-free, automated manner within several milliseconds.