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Cytokinin activity of N6-benzyladenine derivatives assayed by interaction with the receptors in planta, in vitro, and in silico.
Savelieva, Ekaterina M; Oslovsky, Vladimir E; Karlov, Dmitry S; Kurochkin, Nikolay N; Getman, Irina A; Lomin, Sergey N; Sidorov, Georgy V; Mikhailov, Sergey N; Osolodkin, Dmitry I; Romanov, Georgy A.
Afiliação
  • Savelieva EM; Laboratory of Signaling Systems of Ontogeny Control, Timiryazev Institute of Plant Physiology, Russian Academy of Sciences, Botanicheskaya 35, 127276 Moscow, Russia. Electronic address: savelievaek@ya.ru.
  • Oslovsky VE; Laboratory of Design and Synthesis of Biologically Active Compounds, Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Vavilov Str. 32, 119991 Russia. Electronic address: vladimiroslovsky@gmail.com.
  • Karlov DS; Skolkovo Institute of Science and Technology, Skolkovo Innovation Center, Moscow, 143026 Russia; Department of Chemistry, Lomonosov Moscow State University, Leninskie Gory 1/3, 119991 Moscow, Russia; Institute of Physiologically Active Compounds, Russian Academy of Sciences, Severny Proezd 1, Cherno
  • Kurochkin NN; Laboratory of Design and Synthesis of Biologically Active Compounds, Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Vavilov Str. 32, 119991 Russia. Electronic address: nikola.76@mail.ru.
  • Getman IA; Laboratory of Signaling Systems of Ontogeny Control, Timiryazev Institute of Plant Physiology, Russian Academy of Sciences, Botanicheskaya 35, 127276 Moscow, Russia. Electronic address: getman_i@mail.ru.
  • Lomin SN; Laboratory of Signaling Systems of Ontogeny Control, Timiryazev Institute of Plant Physiology, Russian Academy of Sciences, Botanicheskaya 35, 127276 Moscow, Russia. Electronic address: losn1@yandex.ru.
  • Sidorov GV; Laboratory of Isotope Labelled Physiologically Active Compounds, Institute of Molecular Genetics, Russian Academy of Sciences, Pl. Akad. Kurchatova 2, 123182 Moscow, Russia. Electronic address: sidgv@img.ras.ru.
  • Mikhailov SN; Laboratory of Design and Synthesis of Biologically Active Compounds, Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Vavilov Str. 32, 119991 Russia. Electronic address: smikh@eimb.ru.
  • Osolodkin DI; Department of Chemistry, Lomonosov Moscow State University, Leninskie Gory 1/3, 119991 Moscow, Russia; Institute of Poliomyelitis and Viral Encephalitides, FSBSI Chumakov FSC R&D IBP RAS, Poselok Instituta Poliomelita 8 bd. 1, Poselenie Moskovsky, Moscow 108819, Russia; Institute of Pharmacy and
  • Romanov GA; Laboratory of Signaling Systems of Ontogeny Control, Timiryazev Institute of Plant Physiology, Russian Academy of Sciences, Botanicheskaya 35, 127276 Moscow, Russia; Department of Molecular Basis of Ontogenesis, Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Len
Phytochemistry ; 149: 161-177, 2018 May.
Article em En | MEDLINE | ID: mdl-29544164
Biological effects of hormones in both plants and animals are based on high-affinity interaction with cognate receptors resulting in their activation. The signal of cytokinins, classical plant hormones, is perceived in Arabidopsis by three homologous membrane receptors: AHK2, AHK3, and CRE1/AHK4. To study the cytokinin-receptor interaction, we used 25 derivatives of potent cytokinin N6-benzyladenine (BA) with substituents in the purine heterocycle and/or in the side chain. The study was focused primarily on individual cytokinin receptors from Arabidopsis. The main in planta assay system was based on Arabidopsis double mutants retaining only one isoform of cytokinin receptors and harboring cytokinin-sensitive reporter gene. Classical cytokinin biotest with Amaranthus seedlings was used as an additional biotest. In parallel, the binding of ligands to individual cytokinin receptors was assessed in the in vitro test system. Quantitative comparison of results of different assays confirmed the partial similarity of ligand-binding properties of receptor isoforms. Substituents at positions 8 and 9 of adenine moiety, elongated linker up to 4 methylene units, and replacement of N6 by sulfur or oxygen have resulted in the suppression of cytokinin activity of the derivative toward all receptors. Introduction of a halogen into position 2 of adenine moiety, on the contrary, often increased the ligand activity, especially toward AHK3. Features both common and distinctive of cytokinin receptors in Arabidopsis and Amaranthus were revealed, highlighting species specificity of the cytokinin perception apparatus. Correlations between the extent to which a compound binds to a receptor in vitro and its ability to activate the same receptor in planta were evaluated for each AHK protein. Interaction patterns between individual receptors and ligands were rationalized by structure analysis and molecular docking in sensory modules of AHK receptors. The best correlation between docking scores and specific binding was observed for AHK3. In addition, receptor-specific ligands have been discovered with unique properties to predominantly activate or block distinct cytokinin receptors. These ligands are promising for practical application and as molecular tools in the study of the cytokinin perception by plant cells.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Adenina / Receptores de Citocinas / Citocininas Idioma: En Revista: Phytochemistry Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Adenina / Receptores de Citocinas / Citocininas Idioma: En Revista: Phytochemistry Ano de publicação: 2018 Tipo de documento: Article