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The active DNA-PK holoenzyme occupies a tensed state in a staggered synaptic complex
- Source :
- Structure, Structure (London, England : 1993), vol 29, iss 5
- Publication Year :
- 2020
-
Abstract
- In the non-homologous end joining (NHEJ) of a DNA double strand break, DNA ends are bound and protected by a large heterotrimeric DNA-PK complex, which synapses across the break to tether the broken ends and initiate the repair program. There is a lack of clarity surrounding the nature of the synaptic complex and the mechanism governing the transition to repair. We report an integrative structure of the synaptic complex at a precision of 13.5A (using crosslinking data and available structures), revealing a symmetric head-to-head arrangement with a large offset in the DNA ends and an extensive end-protection mechanism involving a previously uncharacterized plug domain. Hydrogen/deuterium exchange mass spectrometry suggests an allosteric pathway connecting DNA end-binding with the kinase domain that places DNA-PK under tension in the kinase-active state. We present a model for the transition from end-protection to repair, in which the synaptic complex facilitates hierarchical processing of the ends and the assembly of a scaffold, supporting displacement of the catalytic subunit and tension release through kinase activity.
- Subjects :
- DNA End-Joining Repair
DNA-Activated Protein Kinase
non-homologous end-joining
non-homologous end joining
synaptic complex
chemistry.chemical_compound
Structural Biology
Heterotrimeric G protein
A-DNA
050207 economics
0303 health sciences
050208 finance
Chemistry
Synaptonemal Complex
030302 biochemistry & molecular biology
05 social sciences
Biological Sciences
Non-homologous end joining
Molecular Docking Simulation
Protein Binding
DNA repair
hydrogen/deuterium exchange
Protein subunit
1.1 Normal biological development and functioning
Allosteric regulation
Biophysics
Article
DNA-PK
03 medical and health sciences
Underpinning research
Information and Computing Sciences
0502 economics and business
Genetics
Humans
crosslinking mass spectrometry
structure
Kinase activity
Molecular Biology
030304 developmental biology
Binding Sites
modeling
Protein kinase domain
Hela Cells
Chemical Sciences
Generic health relevance
Holoenzymes
DNA
HeLa Cells
Subjects
Details
- ISSN :
- 18784186
- Volume :
- 29
- Issue :
- 5
- Database :
- OpenAIRE
- Journal :
- Structure (London, England : 1993)
- Accession number :
- edsair.doi.dedup.....4088d78931fc93363a73aec75a563855