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Neutron Scattering Provides New Insight into Protein Substrate Processing

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AAA+ ATPases are a large family of ubiquitous enzymes with multiple tasks, including the remodelling of the cellular proteome. A subfamily, so-called unfoldases, recognize, unfold, and address misfolded or dysfunctional proteins towards proteolytic complexes, which eliminate these potentially toxic proteins for a healthy, functional state of the cellular proteome. Given the intrinsic flexibility of ATPases and the transient character of the interaction with their protein substrates, it is challenging in structural biology to follow the conformational changes of these enzyme-substrate complexes during the active unfolding process.

In a collaboration between ILL and IBS (Institut de Biologie Structurale) a novel approach was developed combining time-resolved small angle neutron scattering (TR-SANS) with online-fluorescence spectroscopy on D22, in order to monitor the PAN unfoldase from the deep-sea Methanocaldococcus jannaschii organism and a Green Fluorescent Protein (GFP) model substrate. By using alternating perdeuteration of both partners and by controlling the enzymatic activity of the hyperthermophilic PAN system by temperature activation at 55-60°C, it was possible to follow conformational changes of both PAN and GFP separately and individually during the active unfolding process at a time resolution of 30 seconds.

The results show the progressive unfolding and aggregation of GFP as well as a concomitant and reversible contraction of the PAN unfoldase during the active reaction. While the methodological approach developed has been designed for this specific project, it is expected that it can be applied to a wide range of biological macromolecular complexes, and provide structural information from individual partners at a time resolution of some seconds.

Ibrahim, Z., Martel, A., Moulin, M., Kim, H. S., Härtlein, M., Franzetti, B., & Gabel, F. (2017). Time-resolved neutron scattering provides new insight into protein substrate processing by a AAA+ unfoldase. Scientific Reports, 7, 40948. doi:10.1038/srep40948

This article has been republished from materials provided by the Institut Laue-Langevin . Note: material may have been edited for length and content. For further information, please contact the cited source.