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用于核磁共振研究的原位光驱动pH调制

In Situ Light-driven pH Modulation for NMR Studies.

作者信息

Barde Aarav, Han Ruixian, Olson Martin A, Tonelli Marco, Rienstra Chad M, Henzler-Wildman Katherine A, Ravula Thirupathi

机构信息

Department of Biochemistry, University of Wisconsin-Madison, Madison, WI, 53706, USA.

Department of Chemistry, University of Wisconsin-Madison, Madison, WI, 53706, USA.

出版信息

Angew Chem Int Ed Engl. 2025 Jun 2;64(23):e202501440. doi: 10.1002/anie.202501440. Epub 2025 Mar 31.

Abstract

Proton exchange is a fundamental chemical event, and NMR provides the most direct readout of protonation events with site-specific resolution. Conventional approaches require manual titration of sample pH to collect a series of NMR spectra at different pH values. This requires extensive sample handling and often results in significant sample loss, leading to reduced signal or the need to prepare additional samples. Here, we introduce a novel approach to control pH in NMR samples using water soluble photoacids, which alters the pH of the solution from near neutral to acidic pH upon in situ photo illumination. We show that the solution pH can be precisely controlled by choice of illumination wavelength and intensity, and sufficient protons are released from the photoacid to achieve meaningful pH change in samples where the molecule of interest has significant buffering capacity, such as a >100 µM protein sample. The pH is monitored in situ using internal standards with pH-sensitive chemical shifts. This method enables precise, calibrated, and noninvasive change of sample pH within an NMR magnet, dramatically reducing the necessary sample handling. These findings highlight the potential of light-induced pH control in NMR experiments and increase the robustness and reliability of pH-dependent studies.

摘要

质子交换是一种基本的化学事件,核磁共振(NMR)能以位点特异性分辨率提供质子化事件最直接的读数。传统方法需要手动滴定样品的pH值,以收集一系列不同pH值下的NMR谱。这需要大量的样品处理,且常常导致大量样品损失,从而导致信号减弱或需要制备额外的样品。在此,我们介绍一种使用水溶性光酸控制NMR样品pH值的新方法,该方法在原位光照射下可使溶液的pH值从近中性变为酸性。我们表明,通过选择光照波长和强度可以精确控制溶液的pH值,并且从光酸中释放出足够的质子,以在目标分子具有显著缓冲能力的样品(如浓度大于100 μM的蛋白质样品)中实现有意义的pH值变化。使用具有pH敏感化学位移的内标原位监测pH值。该方法能够在NMR磁体内部精确、校准且无创地改变样品的pH值,极大地减少了必要的样品处理。这些发现突出了光诱导pH控制在NMR实验中的潜力,并提高了pH依赖性研究的稳健性和可靠性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/213e/12124344/1c93339535c9/ANIE-64-e202501440-g001.jpg

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