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De novo determination of mosquitocidal Cry11Aa and Cry11Ba structures from naturally-occurring nanocrystals

Author

Listed:
  • Guillaume Tetreau

    (Univ. Grenoble Alpes, CNRS, CEA, Institut de Biologie Structurale)

  • Michael R. Sawaya

    (University of California)

  • Elke Zitter

    (Univ. Grenoble Alpes, CNRS, CEA, Institut de Biologie Structurale)

  • Elena A. Andreeva

    (Univ. Grenoble Alpes, CNRS, CEA, Institut de Biologie Structurale
    Max-Planck-Institut für medizinische Forschung)

  • Anne-Sophie Banneville

    (Univ. Grenoble Alpes, CNRS, CEA, Institut de Biologie Structurale)

  • Natalie A. Schibrowsky

    (University of California
    University of California)

  • Nicolas Coquelle

    (Institut Laue-Langevin)

  • Aaron S. Brewster

    (Lawrence Berkeley National Laboratory)

  • Marie Luise Grünbein

    (Max-Planck-Institut für medizinische Forschung)

  • Gabriela Nass Kovacs

    (Max-Planck-Institut für medizinische Forschung)

  • Mark S. Hunter

    (SLAC National Accelerator Laboratory)

  • Marco Kloos

    (Max-Planck-Institut für medizinische Forschung
    European XFEL GmbH)

  • Raymond G. Sierra

    (SLAC National Accelerator Laboratory)

  • Giorgio Schiro

    (Univ. Grenoble Alpes, CNRS, CEA, Institut de Biologie Structurale)

  • Pei Qiao

    (Texas A&M University)

  • Myriam Stricker

    (Max-Planck-Institut für medizinische Forschung)

  • Dennis Bideshi

    (University of California
    California Baptist University)

  • Iris D. Young

    (Lawrence Berkeley National Laboratory)

  • Ninon Zala

    (Univ. Grenoble Alpes, CNRS, CEA, Institut de Biologie Structurale)

  • Sylvain Engilberge

    (Univ. Grenoble Alpes, CNRS, CEA, Institut de Biologie Structurale)

  • Alexander Gorel

    (Max-Planck-Institut für medizinische Forschung)

  • Luca Signor

    (Univ. Grenoble Alpes, CNRS, CEA, Institut de Biologie Structurale)

  • Jean-Marie Teulon

    (Univ. Grenoble Alpes, CNRS, CEA, Institut de Biologie Structurale)

  • Mario Hilpert

    (Max-Planck-Institut für medizinische Forschung)

  • Lutz Foucar

    (Max-Planck-Institut für medizinische Forschung)

  • Johan Bielecki

    (European XFEL GmbH)

  • Richard Bean

    (European XFEL GmbH)

  • Raphael Wijn

    (European XFEL GmbH)

  • Tokushi Sato

    (European XFEL GmbH)

  • Henry Kirkwood

    (European XFEL GmbH)

  • Romain Letrun

    (European XFEL GmbH)

  • Alexander Batyuk

    (SLAC National Accelerator Laboratory)

  • Irina Snigireva

    (European Synchrotron Radiation Facility (ESRF), BP 220)

  • Daphna Fenel

    (Univ. Grenoble Alpes, CNRS, CEA, Institut de Biologie Structurale)

  • Robin Schubert

    (European XFEL GmbH)

  • Ethan J. Canfield

    (University of Southern California)

  • Mario M. Alba

    (University of Southern California)

  • Frédéric Laporte

    (Univ. Grenoble Alpes, CNRS, LECA)

  • Laurence Després

    (Univ. Grenoble Alpes, CNRS, LECA)

  • Maria Bacia

    (Univ. Grenoble Alpes, CNRS, CEA, Institut de Biologie Structurale)

  • Amandine Roux

    (Université Claude Bernard Lyon 1, Laboratoire de Chimie)

  • Christian Chapelle

    (Polyvalan SARL)

  • François Riobé

    (Université Claude Bernard Lyon 1, Laboratoire de Chimie)

  • Olivier Maury

    (Université Claude Bernard Lyon 1, Laboratoire de Chimie)

  • Wai Li Ling

    (Univ. Grenoble Alpes, CNRS, CEA, Institut de Biologie Structurale)

  • Sébastien Boutet

    (SLAC National Accelerator Laboratory)

  • Adrian Mancuso

    (European XFEL GmbH)

  • Irina Gutsche

    (Univ. Grenoble Alpes, CNRS, CEA, Institut de Biologie Structurale)

  • Eric Girard

    (Univ. Grenoble Alpes, CNRS, CEA, Institut de Biologie Structurale)

  • Thomas R. M. Barends

    (Max-Planck-Institut für medizinische Forschung)

  • Jean-Luc Pellequer

    (Univ. Grenoble Alpes, CNRS, CEA, Institut de Biologie Structurale)

  • Hyun-Woo Park

    (University of California
    California Baptist University)

  • Arthur D. Laganowsky

    (Texas A&M University)

  • Jose Rodriguez

    (University of California
    University of California)

  • Manfred Burghammer

    (European Synchrotron Radiation Facility (ESRF), BP 220)

  • Robert L. Shoeman

    (Max-Planck-Institut für medizinische Forschung)

  • R. Bruce Doak

    (Max-Planck-Institut für medizinische Forschung)

  • Martin Weik

    (Univ. Grenoble Alpes, CNRS, CEA, Institut de Biologie Structurale)

  • Nicholas K. Sauter

    (Lawrence Berkeley National Laboratory)

  • Brian Federici

    (University of California)

  • Duilio Cascio

    (University of California)

  • Ilme Schlichting

    (Max-Planck-Institut für medizinische Forschung)

  • Jacques-Philippe Colletier

    (Univ. Grenoble Alpes, CNRS, CEA, Institut de Biologie Structurale)

Abstract

Cry11Aa and Cry11Ba are the two most potent toxins produced by mosquitocidal Bacillus thuringiensis subsp. israelensis and jegathesan, respectively. The toxins naturally crystallize within the host; however, the crystals are too small for structure determination at synchrotron sources. Therefore, we applied serial femtosecond crystallography at X-ray free electron lasers to in vivo-grown nanocrystals of these toxins. The structure of Cry11Aa was determined de novo using the single-wavelength anomalous dispersion method, which in turn enabled the determination of the Cry11Ba structure by molecular replacement. The two structures reveal a new pattern for in vivo crystallization of Cry toxins, whereby each of their three domains packs with a symmetrically identical domain, and a cleavable crystal packing motif is located within the protoxin rather than at the termini. The diversity of in vivo crystallization patterns suggests explanations for their varied levels of toxicity and rational approaches to improve these toxins for mosquito control.

Suggested Citation

  • Guillaume Tetreau & Michael R. Sawaya & Elke Zitter & Elena A. Andreeva & Anne-Sophie Banneville & Natalie A. Schibrowsky & Nicolas Coquelle & Aaron S. Brewster & Marie Luise Grünbein & Gabriela Nass , 2022. "De novo determination of mosquitocidal Cry11Aa and Cry11Ba structures from naturally-occurring nanocrystals," Nature Communications, Nature, vol. 13(1), pages 1-18, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-31746-x
    DOI: 10.1038/s41467-022-31746-x
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    1. Robert Schönherr & Juliane Boger & J. Mia Lahey-Rudolph & Mareike Harms & Jacqueline Kaiser & Sophie Nachtschatt & Marla Wobbe & Rainer Duden & Peter König & Gleb Bourenkov & Thomas R. Schneider & Lar, 2024. "A streamlined approach to structure elucidation using in cellulo crystallized recombinant proteins, InCellCryst," Nature Communications, Nature, vol. 15(1), pages 1-17, December.

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