Sarter Mona, Stewart J Ross, Nilsen Gøran Jan, Devonport Mark, Nemkovski Kirill
STFC Rutherford Appleton Laboratory, ISIS Neutron and Muon Facility, Chilton, Didcot OX11 0QX, U.K.
J Am Chem Soc. 2024 Oct 3;146(41):28023-33. doi: 10.1021/jacs.4c06273.
Protein dynamics play a vital role in biology. Quasi elastic neutron scattering (QENS) is an ideal method to access these dynamics. To isolate protein dynamics, it is important to separate the signal of the buffer and the protein. Normally data analysis is performed based on the assumption that the scattering spectrum is incoherent. To observe the full range of protein dynamics, it is necessary to perform the experiments in solution. This solution is usually a fully deuterated buffer, while the protein remains protonated. It is generally assumed that subtracting the buffer contribution removes all coherent signal from the measured spectrum, and the rest can be considered as purely incoherent. Up until recently, there was no way to experimentally verify this assumption. Polarized QENS experiments allow for the coherent and incoherent contributions to be separated. By comparing the results from the polarized QENS experiment and the standard analysis method from unpolarized QENS, we are thus able to check this assumption experimentally. We show that the pure incoherent spectrum obtained from polarization analysis does not match the results for unpolarized QENS. We discuss the implications of this for data analysis and possible solutions to the problem, as well as mitigation techniques for standard QENS.
蛋白质动力学在生物学中起着至关重要的作用。准弹性中子散射(QENS)是研究这些动力学的理想方法。为了分离出蛋白质动力学,将缓冲液和蛋白质的信号区分开来很重要。通常,数据分析是基于散射光谱是非相干的这一假设进行的。为了观察蛋白质动力学的完整范围,有必要在溶液中进行实验。这种溶液通常是完全氘代的缓冲液,而蛋白质保持质子化状态。一般认为,减去缓冲液的贡献就能从测量光谱中去除所有相干信号,剩下的可以视为纯非相干信号。直到最近,还没有办法通过实验验证这一假设。极化QENS实验能够分离相干和非相干贡献。通过比较极化QENS实验的结果和非极化QENS的标准分析方法,我们因此能够通过实验检验这一假设。我们表明,从极化分析获得的纯非相干光谱与非极化QENS的结果不匹配。我们讨论了这对数据分析的影响以及该问题的可能解决方案,还有标准QENS的缓解技术。