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Allosteric modulation of the GTPase activity of a bacterial LRRK2 homologue by conformation-specific Nanobodies

Leemans, M., Galicia, C., Deyaert, E., Daems, E., Krause, L., Paesmans, J., Pardon, E., Steyaert, J., Kortholt, A., Sobott, F., Klostermeier, D. & Versées, W., Apr-2020, In : Biochemical Journal. 477, 7, p. 1203-1218 16 p.

Research output: Contribution to journalArticleAcademicpeer-review

  • Margaux Leemans
  • Christian Galicia
  • Egon Deyaert
  • Elise Daems
  • Linda Krause
  • Jone Paesmans
  • Els Pardon
  • Jan Steyaert
  • Arjan Kortholt
  • Frank Sobott
  • Dagmar Klostermeier
  • Wim Versées

Mutations in the Parkinson's disease (PD)-associated protein leucine-rich repeat kinase 2 (LRRK2) commonly lead to a reduction of GTPase activity and increase in kinase activity. Therefore, strategies for drug development have mainly been focusing on the design of LRRK2 kinase inhibitors. We recently showed that the central RocCOR domains (Roc: Ras of complex proteins; COR: C-terminal of Roc) of a bacterial LRRK2 homologue cycle between a dimeric and monomeric form concomitant with GTP binding and hydrolysis. PD-associated mutations can slow down GTP hydrolysis by stabilizing the protein in its dimeric form. Here, we report the identification of two Nanobodies (NbRoco1 and NbRoco2) that bind the bacterial Roco protein (CtRoco) in a conformation-specific way, with a preference for the GTP-bound state. NbRoco1 considerably increases the GTPase turnover of CtRoco and reverts the decrease in GTPase activity caused by a PD-analogous mutation. We show that NbRoco1 exerts its effect by allosterically interfering with the CtRoco dimer-monomer cycle through destabilization of the dimeric form. Hence, we provide the first proof of principle that allosteric modulation of the RocCOR dimer-monomer cycle can alter its GTPase activity, which might present a potential novel strategy to overcome the effect of LRRK2 PD mutations.

Original languageEnglish
Pages (from-to)1203-1218
Number of pages16
JournalBiochemical Journal
Volume477
Issue number7
Early online date2020
Publication statusPublished - Apr-2020

    Keywords

  • GENOME-WIDE ASSOCIATION, PARKINSONS-DISEASE, MOLECULAR INSIGHTS, KINASE INHIBITION, MUTATION, PROTEIN, DOMAIN, METAANALYSIS, DISCOVERY, DYNAMICS

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