Department of Electrical Engineering, Indian Institute of Science, Bangalore, 560012, India.
NMR Research Centre, Indian Institute of Science, Bangalore, 560012, India.
Sci Rep. 2017 Aug 29;7(1):9651. doi: 10.1038/s41598-017-09884-w.
We present a novel method that breaks the resolution barrier in nuclear magnetic resonance (NMR) spectroscopy, allowing one to accurately estimate the chemical shift values of highly overlapping or broadened peaks. This problem is routinely encountered in NMR when peaks have large linewidths due to rapidly decaying signals, hindering its application. We address this problem based on the notion of finite-rate-of-innovation (FRI) sampling, which is based on the premise that signals such as the NMR signal, can be accurately reconstructed using fewer measurements than that required by existing approaches. The FRI approach leads to super-resolution, beyond the limits of contemporary NMR techniques. Using this method, we could measure for the first time small changes in chemical shifts during the formation of a Gold nanorod-protein complex, facilitating the quantification of the strength of such interactions. The method thus opens up new possibilities for the application and acceleration of multidimensional NMR spectroscopy across a wide range of systems.
我们提出了一种新方法,突破了核磁共振(NMR)光谱学中的分辨率限制,能够准确估计高度重叠或展宽峰的化学位移值。当由于信号迅速衰减而导致峰具有较大的线宽时,NMR 中经常会遇到这个问题,这限制了其应用。我们基于有限的创新率(FRI)采样的概念来解决这个问题,该概念基于这样的前提,即可以使用比现有方法所需的测量值更少的测量值来准确重建诸如 NMR 信号之类的信号。FRI 方法可实现超越当前 NMR 技术限制的超分辨率。使用这种方法,我们首次可以在金纳米棒-蛋白质复合物形成过程中测量化学位移的微小变化,从而便于对这种相互作用的强度进行定量。因此,该方法为在广泛的系统中应用和加速多维 NMR 光谱学开辟了新的可能性。