Unknown

Dataset Information

0

Charge as a selection criterion for translocation through the nuclear pore complex.


ABSTRACT: Nuclear pore complexes (NPCs) are highly selective filters that control the exchange of material between nucleus and cytoplasm. The principles that govern selective filtering by NPCs are not fully understood. Previous studies find that cellular proteins capable of fast translocation through NPCs (transport receptors) are characterized by a high proportion of hydrophobic surface regions. Our analysis finds that transport receptors and their complexes are also highly negatively charged. Moreover, NPC components that constitute the permeability barrier are positively charged. We estimate that electrostatic interactions between a transport receptor and the NPC result in an energy gain of several k(B)T, which would enable significantly increased translocation rates of transport receptors relative to other cellular proteins. We suggest that negative charge is an essential criterion for selective passage through the NPC.

SUBMITTER: Colwell LJ 

PROVIDER: S-EPMC2858669 | biostudies-literature | 2010 Apr

REPOSITORIES: biostudies-literature

altmetric image

Publications

Charge as a selection criterion for translocation through the nuclear pore complex.

Colwell Lucy J LJ   Brenner Michael P MP   Ribbeck Katharina K  

PLoS computational biology 20100422 4


Nuclear pore complexes (NPCs) are highly selective filters that control the exchange of material between nucleus and cytoplasm. The principles that govern selective filtering by NPCs are not fully understood. Previous studies find that cellular proteins capable of fast translocation through NPCs (transport receptors) are characterized by a high proportion of hydrophobic surface regions. Our analysis finds that transport receptors and their complexes are also highly negatively charged. Moreover,  ...[more]

Similar Datasets

| S-EPMC2064648 | biostudies-literature
| S-EPMC516490 | biostudies-literature
| S-EPMC2557044 | biostudies-other
| S-EPMC6146805 | biostudies-literature
| S-EPMC4764519 | biostudies-literature
| S-EPMC3296253 | biostudies-literature
| S-EPMC5057280 | biostudies-literature