Substrate-dependent activation of LONP1 informs on proteolytic regulation and ATPase motor function

AAA+ enzymes use energy from ATP hydrolysis to remodel diverse cellular targets. Structures of substrate-bound AAA+ complexes suggest that these enzymes employ a conserved hand-over-hand mechanism to thread substrates through their central pore. However, the fundamental aspects of the mechanisms governing motor function and substrate processing within specific AAA+ families remain unresolved. We used cryoelectron microscopy to structurally interrogate reaction intermediates from in vitro biochemical assays to inform the underlying regulatory mechanisms of the human mitochondrial AAA+ protease, LONP1. Our results demonstrate that substrate binding, rather than nucleotide binding, activates the assembly and allosterically regulates proteolytic activity. The N-terminal domain plays a critical role in this process and facilitates the initial stages of substrate selection and engagement. Moreover, structures of LONP1 actively degrading a substrate in the presence of ATP provide important context to the conventional understanding of the hand-over-hand translocation mechanism, suggesting that ATP hydrolysis is likely not limited to a single position in the right-handed spiral during the hand-over-hand translocation mechanism.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2025-10-15
DOI
https://doi.org/10.1073/pnas.2415153122
Citations
1
Primary Topic
ATP Synthase and ATPases Research
Type
article
Field-Weighted Citation Impact
0.81
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article

Substrate-dependent activation of LONP1 informs on proteolytic regulation and ATPase motor function

Gabriel C. Lander, Jeffrey T. Mindrebo
1 citations
Proceedings of the National Academy of Sciences
ATP Synthase and ATPases Research
0.81
article

Substrate-dependent activation of LONP1 informs on proteolytic regulation and ATPase motor function

Gabriel C. Lander, Jeffrey T. Mindrebo
article en
1 citations

Abstract

AAA+ enzymes use energy from ATP hydrolysis to remodel diverse cellular targets. Structures of substrate-bound AAA+ complexes suggest that these enzymes employ a conserved hand-over-hand mechanism to thread substrates through their central pore. However, the fundamental aspects of the mechanisms governing motor function and substrate processing within specific AAA+ families remain unresolved. We used cryoelectron microscopy to structurally interrogate reaction intermediates from in vitro biochemical assays to inform the underlying regulatory mechanisms of the human mitochondrial AAA+ protease, LONP1. Our results demonstrate that substrate binding, rather than nucleotide binding, activates the assembly and allosterically regulates proteolytic activity. The N-terminal domain plays a critical role in this process and facilitates the initial stages of substrate selection and engagement. Moreover, structures of LONP1 actively degrading a substrate in the presence of ATP provide important context to the conventional understanding of the hand-over-hand translocation mechanism, suggesting that ATP hydrolysis is likely not limited to a single position in the right-handed spiral during the hand-over-hand translocation mechanism.

Proceedings of the National Academy of SciencesVol. 122(42)
Scripps Research Institute (US), Scripps (United States) (US)
Openalex Percentile: Top 22%
ATP Synthase and ATPases Research
0.81
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Substrate-dependent activation of LONP1 informs on proteolytic regulation and ATPase motor function — Gabriel C. Lander, Jeffrey T. Mindrebo · Proceedings of the National Academy of Sciences (2025) | TGRS Research Map | TGRS