Bernardo Gabiatti

This study identifies a direct interaction between the RNA helicase KREH2 and the RESC1-RESC2 complex in trypanosomatid mitochondrial RNA editing using biochemical and structural methods.

This study shows that Trypanosoma brucei lacks a functional EJC and NMD pathway due to intron loss and gene redundancy.

The paper uses expansion microscopy and proximity labeling to reveal an asymmetric nuclear pore structure in trypanosomes, identifying unique and conserved components involved in mRNA export.

The paper identifies two distinct eIF4F complexes in Trypanosoma cruzi that bind different mRNAs and show altered associations under nutritional stress.

This paper demonstrates that streptavidin-based imaging outperforms immunofluorescence in detecting low-abundance or inaccessible proteins and reveals dynamic protein interactions.