Unknown

Dataset Information

0

Cell type-specific nuclear pores: a case in point for context-dependent stoichiometry of molecular machines.


ABSTRACT: To understand the structure and function of large molecular machines, accurate knowledge of their stoichiometry is essential. In this study, we developed an integrated targeted proteomics and super-resolution microscopy approach to determine the absolute stoichiometry of the human nuclear pore complex (NPC), possibly the largest eukaryotic protein complex. We show that the human NPC has a previously unanticipated stoichiometry that varies across cancer cell types, tissues and in disease. Using large-scale proteomics, we provide evidence that more than one third of the known, well-defined nuclear protein complexes display a similar cell type-specific variation of their subunit stoichiometry. Our data point to compositional rearrangement as a widespread mechanism for adapting the functions of molecular machines toward cell type-specific constraints and context-dependent needs, and highlight the need of deeper investigation of such structural variants.

SUBMITTER: Ori A 

PROVIDER: S-EPMC3619942 | biostudies-literature |

REPOSITORIES: biostudies-literature

Similar Datasets

| S-EPMC4732213 | biostudies-literature
| S-EPMC3947552 | biostudies-literature
| S-EPMC5180592 | biostudies-literature
| S-EPMC7206255 | biostudies-literature
| S-EPMC6479675 | biostudies-literature
2023-08-19 | GSE216888 | GEO
| S-EPMC10657382 | biostudies-literature
| S-EPMC6838685 | biostudies-literature
| S-EPMC4967450 | biostudies-literature
| S-EPMC3587839 | biostudies-other