Physical review. EBiophysicsPeer-reviewed journal article
Polarized neutrons for the study of individual and collective fast dynamics in proteins
AnonymousiD, Jacques OllivieriD, J. R. StewartiD, Judith PetersiD
Abstract
Neutron scattering is a powerful technique to investigate atomic structures and molecular dynamics of proteins at the nano-scale. When it comes to dynamics, incoherent and coherent scattering respectively provide information on the single and collective dynamics of nuclei. In proteins, hydrogen has the highest incoherent cross-section, and it is common practice to overlook the contribution of coherent terms stemming from all nuclei. However, the fast collective dynamics of heavier nuclei could also be studied if coherent scattering and incoherent scattering were experimentally separated. The recent advent of polarized neutron spectroscopy with sufficient flux and energy resolution has made it possible, and opens new perspectives to investigate the relative importance of coherent scattering and the information it provides on biological samples. The present study reports on the use of polarized quasi-elastic neutron scattering (QENS) and the application of a minimalistic model adapted to both individual and collective dynamics. Using a perdeuterated green fluorescent protein as a model globular protein, the study provides an interpretation of the dynamical parameters obtained with QENS, and a comparative study of the Elastic Coherent and Incoherent Scattering Factor. Based on both experiments and calculations, we discuss the relative importance of distinct and self components of coherent scattering, which is often wrongly assumed to be representative of collective dynamics only. The results highlight the current impediments rendering complicated a straightforward analysis of fast collective dynamics in hydrated protein samples.
- Citations
- 1
- FWCI
- 3.85
- Field percentile
- top 5%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Changes in protein dynamical parameters derived from quasi-elastic neutron scattering spectra induced by coherent scattering: A molecular dynamics simulation study
T. Matsuo·bioRxiv·Oct 27, 2022
- Effects of heavy water on protein dynamics studied by molecular dynamics simulation: Focusing on dynamical parameters obtained by quasi-elastic neutron scattering
T. Matsuo·bioRxiv·Sep 8, 2022
- Decoupling of the Onset of Anharmonicity between a Protein and Its Surface Water around 200 K
- Molecular dynamics ensemble refinement of the heterogeneous native state of NCBD using chemical shifts and NOEs
E. Papaleo, C. Camilloni, … K. Lindorff-Larsen·bioRxiv·Feb 28, 2018
- Internal Protein Motions in Molecular Dynamics Simulations of Bragg and Diffuse X-ray Scattering
M. Wall·bioRxiv·Sep 26, 2017
- Fractionation-Free Protein Corona Quantification Through Synchrotron-Based Small-Angle X-ray Scattering
Juliana Tosta Theodoro Carvalho, Caroline E.P. Silva, … Mateus Borba Cardoso·Small MethodsPeer-reviewed·Jun 29, 2026