Structural basis for the ligand promiscuity of the neofunctionalized, carotenoid-binding fasciclin domain protein AstaP.


Journal

Communications biology
ISSN: 2399-3642
Titre abrégé: Commun Biol
Pays: England
ID NLM: 101719179

Informations de publication

Date de publication:
28 04 2023
Historique:
received: 26 01 2023
accepted: 10 04 2023
medline: 1 5 2023
pubmed: 29 4 2023
entrez: 28 4 2023
Statut: epublish

Résumé

Fasciclins (FAS1) are ancient adhesion protein domains with no common small ligand binding reported. A unique microalgal FAS1-containing astaxanthin (AXT)-binding protein (AstaP) binds a broad repertoire of carotenoids by a largely unknown mechanism. Here, we explain the ligand promiscuity of AstaP-orange1 (AstaPo1) by determining its NMR structure in complex with AXT and validating this structure by SAXS, calorimetry, optical spectroscopy and mutagenesis. α1-α2 helices of the AstaPo1 FAS1 domain embrace the carotenoid polyene like a jaw, forming a hydrophobic tunnel, too short to cap the AXT β-ionone rings and dictate specificity. AXT-contacting AstaPo1 residues exhibit different conservation in AstaPs with the tentative carotenoid-binding function and in FAS1 proteins generally, which supports the idea of AstaP neofunctionalization within green algae. Intriguingly, a cyanobacterial homolog with a similar domain structure cannot bind carotenoids under identical conditions. These structure-activity relationships provide the first step towards the sequence-based prediction of the carotenoid-binding FAS1 members.

Identifiants

pubmed: 37117801
doi: 10.1038/s42003-023-04832-z
pii: 10.1038/s42003-023-04832-z
pmc: PMC10147662
doi:

Substances chimiques

Carrier Proteins 0
Ligands 0
Cell Adhesion Molecules 0
Carotenoids 36-88-4

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

471

Informations de copyright

© 2023. The Author(s).

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Auteurs

Fedor D Kornilov (FD)

Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences, 117997, Moscow, Russia.
Moscow Institute of Physics and Technology, 141701, Dolgoprudny, Russia.

Yury B Slonimskiy (YB)

A.N. Bach Institute of Biochemistry, Federal Research Center of Biotechnology of the Russian Academy of Sciences, 119071, Moscow, Russia.

Daria A Lunegova (DA)

A.N. Bach Institute of Biochemistry, Federal Research Center of Biotechnology of the Russian Academy of Sciences, 119071, Moscow, Russia.

Nikita A Egorkin (NA)

A.N. Bach Institute of Biochemistry, Federal Research Center of Biotechnology of the Russian Academy of Sciences, 119071, Moscow, Russia.

Anna G Savitskaya (AG)

Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences, 117997, Moscow, Russia.

Sergey Yu Kleymenov (SY)

Koltzov Institute of Developmental Biology of the Russian Academy of Sciences, 26 Vavilov Street, 119334, Moscow, Russia.

Eugene G Maksimov (EG)

M.V. Lomonosov Moscow State University, Faculty of Biology, 119991, Moscow, Russia.

Sergey A Goncharuk (SA)

Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences, 117997, Moscow, Russia.
Moscow Institute of Physics and Technology, 141701, Dolgoprudny, Russia.

Konstantin S Mineev (KS)

Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences, 117997, Moscow, Russia. konstantin.mineev@gmail.com.
Moscow Institute of Physics and Technology, 141701, Dolgoprudny, Russia. konstantin.mineev@gmail.com.

Nikolai N Sluchanko (NN)

A.N. Bach Institute of Biochemistry, Federal Research Center of Biotechnology of the Russian Academy of Sciences, 119071, Moscow, Russia. nikolai.sluchanko@mail.ru.

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