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Redox-Sensitive Cysteines Confer Proximal Control of the Molecular Crowding Barrier in the Nuclear Pore
- Source :
- Cell Reports, Vol 33, Iss 11, Pp 108484-(2020)
- Publication Year :
- 2020
- Publisher :
- Elsevier BV, 2020.
-
Abstract
- The nuclear pore complex forms a highly crowded selective barrier with intrinsically disordered regions at the nuclear membrane to coordinate nucleocytoplasmic molecular communications. Although oxidative stress is known to alter the barrier function, the molecular mechanism underlying this adaptive control of the nuclear pore complex remains unknown. Here we uncover a systematic control of the crowding barrier within the nuclear pore in response to various redox environments. Direct measurements of the crowding states using a crowding-sensitive FRET (Förster resonance energy transfer) probe reveal specific roles of the nuclear pore subunits that adjust the degree of crowding in response to different redox conditions, by adaptively forming or disrupting redox-sensitive disulfide bonds. Relationships between crowding control and the barrier function of the nuclear pore are investigated by single-molecular fluorescence measurements of nuclear transport. Based on these findings, we propose a proximal control model of molecular crowding in vivo that is dynamically regulated at the molecular level.<br />酸化ストレスが細胞の核膜機能を変える機構を解明 --環境に応じて分子の「混み具合」が変わる仕組み--. 京都大学プレスリリース. 2020-12-16.
- Subjects :
- 0301 basic medicine
genetic structures
nuclear transport
Redox
General Biochemistry, Genetics and Molecular Biology
03 medical and health sciences
0302 clinical medicine
molecular crowding
nuclear pore complex
medicine
Humans
oxidative stress
Cysteine
Nuclear membrane
Nuclear pore
lcsh:QH301-705.5
Barrier function
Chemistry
nucleoporin
Crowding
030104 developmental biology
medicine.anatomical_structure
Förster resonance energy transfer
lcsh:Biology (General)
Nuclear Pore
redox response
Biophysics
Nucleoporin
Nuclear transport
Oxidation-Reduction
030217 neurology & neurosurgery
Subjects
Details
- ISSN :
- 22111247
- Volume :
- 33
- Database :
- OpenAIRE
- Journal :
- Cell Reports
- Accession number :
- edsair.doi.dedup.....cc0dccc703d5a238b6bf2d16ef7f2772
- Full Text :
- https://doi.org/10.1016/j.celrep.2020.108484