Počet záznamů: 1  

Auxin molecular field maps define AUX1 selectivity: many auxin herbicides are not substrates

  1. 1.
    0488687 - ÚEB 2019 RIV GB eng J - Článek v odborném periodiku
    Hoyerová, Klára - Hošek, Petr - Quareshy, M. - Li, J. - Klíma, Petr - Kubeš, Martin - Yemm, A. A. - Neve, P. - Tripathi, A. - Bennett, M.J. - Napier, R. M.
    Auxin molecular field maps define AUX1 selectivity: many auxin herbicides are not substrates.
    New Phytologist. Roč. 217, č. 4 (2018), s. 1625-1639. ISSN 0028-646X. E-ISSN 1469-8137
    Grant CEP: GA ČR(CZ) GA16-19557S; GA MŠMT LD15137
    Grant ostatní: OPPK(XE) CZ.2.16/3.1.00/21519
    Institucionální podpora: RVO:61389030
    Klíčová slova: auxin transport * cheminformatics * herbicide * herbicide resistance * molecular field maps * pharmacophore * structure–activity relationship * uptake carrier
    Obor OECD: Cell biology
    Impakt faktor: 7.299, rok: 2018

    Developmental responses to auxin are regulated by facilitated uptake and efflux, but detailed molecular understanding of the carrier proteins is incomplete. We have used pharmacological tools to explore the chemical space that defines substrate preferences for the auxin uptake carrier AUX1. Total and partial loss-of-function aux1 mutants were assessed against wild-type for dose-dependent resistance to a range of auxins and analogues. We then developed an auxin accumulation assay with associated mathematical modelling to enumerate accurate IC 50 values for a small library of auxin analogues. The structure activity relationship data were analysed using molecular field analyses to create a pharmacophoric atlas of AUX1 substrates. The uptake carrier exhibits a very high level of selectivity towards small substrates including the natural indole-3-acetic acid, and the synthetic auxin 2,4-dichlorophenoxyacetic acid. No AUX1 activity was observed for herbicides based on benzoic acid (dicamba), pyridinyloxyacetic acid (triclopyr) or the 6-arylpicolinates (halauxifen), and very low affinity was found for picolinic acid-based auxins (picloram) and quinolinecarboxylic acids (quinclorac). The atlas demonstrates why some widely used auxin herbicides are not, or are very poor substrates. We list molecular descriptors for AUX1 substrates and discuss our findings in terms of herbicide resistance management.
    Trvalý link: http://hdl.handle.net/11104/0283238

     
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