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8AQI

NanoLuc luciferase with bound coelenteramide in surface allosteric site

Summary for 8AQI
Entry DOI10.2210/pdb8aqi/pdb
DescriptorNanoLuc luciferase, N-[3-BENZYL-5-(4-HYDROXYPHENYL)PYRAZIN-2-YL]-2-(4-HYDROXYPHENYL)ACETAMIDE, CHLORIDE ION, ... (5 entities in total)
Functional Keywordsluciferase, nanoluc, nluc, luciferin, coelenterazine, luminescent protein
Biological sourceOplophorus gracilirostris
Total number of polymer chains8
Total formula weight165051.30
Authors
Nemergut, M.,Marek, M. (deposition date: 2022-08-12, release date: 2023-08-23, Last modification date: 2023-12-27)
Primary citationNemergut, M.,Pluskal, D.,Horackova, J.,Sustrova, T.,Tulis, J.,Barta, T.,Baatallah, R.,Gagnot, G.,Novakova, V.,Majerova, M.,Sedlackova, K.,Marques, S.M.,Toul, M.,Damborsky, J.,Prokop, Z.,Bednar, D.,Janin, Y.L.,Marek, M.
Illuminating the mechanism and allosteric behavior of NanoLuc luciferase.
Nat Commun, 14:7864-7864, 2023
Cited by
PubMed Abstract: NanoLuc, a superior β-barrel fold luciferase, was engineered 10 years ago but the nature of its catalysis remains puzzling. Here experimental and computational techniques are combined, revealing that imidazopyrazinone luciferins bind to an intra-barrel catalytic site but also to an allosteric site shaped on the enzyme surface. Structurally, binding to the allosteric site prevents simultaneous binding to the catalytic site, and vice versa, through concerted conformational changes. We demonstrate that restructuration of the allosteric site can boost the luminescent reaction in the remote active site. Mechanistically, an intra-barrel arginine coordinates the imidazopyrazinone component of luciferin, which reacts with O via a radical charge-transfer mechanism, and then it also protonates the resulting excited amide product to form a light-emitting neutral species. Concomitantly, an aspartate, supported by two tyrosines, fine-tunes the blue color emitter to secure a high emission intensity. This information is critical to engineering the next-generation of ultrasensitive bioluminescent reporters.
PubMed: 38030625
DOI: 10.1038/s41467-023-43403-y
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.99 Å)
Structure validation

226707

数据于2024-10-30公开中

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