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Interactions of nuclear transport factors and surface-conjugated FG nucleoporins: Insights and limitations.


ABSTRACT: Protein-protein interactions are central to biological processes. In vitro methods to examine protein-protein interactions are generally categorized into two classes: in-solution and surface-based methods. Here, using the multivalent interactions between nucleocytoplasmic transport factors and intrinsically disordered FG repeat containing nuclear pore complex proteins as a model system, we examined the utility of three surface-based methods: atomic force microscopy, quartz crystal microbalance with dissipation, and surface plasmon resonance. Although results were comparable to those of previous reports, the apparent effect of mass transport limitations was demonstrated. Additional experiments with a loss-of-interaction FG repeat mutant variant demonstrated that the binding events that take place on surfaces can be unexpectedly complex, suggesting particular care must be exercised in interpretation of such data.

SUBMITTER: Hayama R 

PROVIDER: S-EPMC6553764 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature

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Interactions of nuclear transport factors and surface-conjugated FG nucleoporins: Insights and limitations.

Hayama Ryo R   Sorci Mirco M   Keating Iv John J JJ   Hecht Lee M LM   Plawsky Joel L JL   Belfort Georges G   Chait Brian T BT   Rout Michael P MP  

PloS one 20190606 6


Protein-protein interactions are central to biological processes. In vitro methods to examine protein-protein interactions are generally categorized into two classes: in-solution and surface-based methods. Here, using the multivalent interactions between nucleocytoplasmic transport factors and intrinsically disordered FG repeat containing nuclear pore complex proteins as a model system, we examined the utility of three surface-based methods: atomic force microscopy, quartz crystal microbalance w  ...[more]

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