8AQI
NanoLuc luciferase with bound coelenteramide in surface allosteric site
Summary for 8AQI
Entry DOI | 10.2210/pdb8aqi/pdb |
Descriptor | NanoLuc luciferase, N-[3-BENZYL-5-(4-HYDROXYPHENYL)PYRAZIN-2-YL]-2-(4-HYDROXYPHENYL)ACETAMIDE, CHLORIDE ION, ... (5 entities in total) |
Functional Keywords | luciferase, nanoluc, nluc, luciferin, coelenterazine, luminescent protein |
Biological source | Oplophorus gracilirostris |
Total number of polymer chains | 8 |
Total formula weight | 165051.30 |
Authors | Nemergut, M.,Marek, M. (deposition date: 2022-08-12, release date: 2023-08-23, Last modification date: 2023-12-27) |
Primary citation | Nemergut, 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: 38030625DOI: 10.1038/s41467-023-43403-y PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.99 Å) |
Structure validation
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