Dynamic Nuclear Polarization-Enabled Quantum Sensing for Investigating Peptide Configurations

IF 1.1 4区 物理与天体物理 Q4 PHYSICS, ATOMIC, MOLECULAR & CHEMICAL Applied Magnetic Resonance Pub Date : 2023-10-04 DOI:10.1007/s00723-023-01617-9
Nour Alnajar, Asif Equbal
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Abstract

Introducing persistent free radicals into biochemical systems, a mechanism referred to as Site-Directed Spin Labeling (SDSL) is a biophysical research feat established by Wayne Hubbell. Integrating double electron–electron resonance (DEER) within SDSL enabled intermolecular distance measurements in the long-range (nanometers) that were otherwise unfeasible using nuclear magnetic resonance (NMR) techniques. DEER is commonly used in the structural analysis of peptides and polymers to probe the distance between electron spin labels (\(r_{ee}\)), typically within the range of 2.0–8.0 nm. However, this technique is generally employed at low-to-intermediate magnetic fields, such as X-Band (0.35 T), Q-Band (1.0 T), or W-Band (3.4 T) mainly due to the microwave power limitation at high fields. This may restrict both the structural resolution and the ability to probe a shorter distance. We propose a novel approach for distance measurement in SDSL peptides or polymers. This approach utilizes dynamic nuclear polarization (DNP) to investigate the distances between unpaired electron spins. DNP is a nuclear spin hyperpolarization technique that has revolutionized solid-state NMR by enhancing its sensitivity. It works by transferring high electron spin polarization to coupled nuclear spins under microwave irradiation. The efficiency of cross-effect DNP transfer is determined by the magnitude of the dipole–dipole coupling between two electron spins. By exploiting the distance dependence between two electron spins, we can sense the configurations of SDSL peptides. One significant advantage of DNP-enabled quantum sensing is that the method can be applied at higher magnetic fields and under magic-angle spinning conditions using existing instrumentation. The approach also enables observation of shorter distances. Overall, our proposed method opens up new possibilities for structural analysis and distance measurements in the study of peptides and polymers, combining with ingenious SDSL technique introduced by the esteemed scientist, Professor Wayne Hubbell.

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用于研究多肽构型的动态核极化量子传感技术
韦恩-哈贝尔(Wayne Hubbell)将持久性自由基引入生化系统,这种机制被称为 "位点定向自旋标记(SDSL)",是生物物理研究的一项壮举。将双电子-电子共振(DEER)整合到 SDSL 中,可实现长距离(纳米)分子间距离测量,而使用核磁共振(NMR)技术则无法实现这一点。DEER 通常用于肽和聚合物的结构分析,以探测电子自旋标签(\(r_{ee}\))之间的距离,通常在 2.0-8.0 纳米范围内。然而,由于高磁场下微波功率的限制,这种技术一般在中低磁场下使用,如 X 波段(0.35 T)、Q 波段(1.0 T)或 W 波段(3.4 T)。这可能会限制结构分辨率和探测较短距离的能力。我们提出了一种测量 SDSL 肽或聚合物距离的新方法。这种方法利用动态核极化(DNP)来研究非配对电子自旋之间的距离。DNP 是一种核自旋超极化技术,通过提高灵敏度彻底改变了固态 NMR。它的工作原理是在微波辐照下将高电子自旋极化转移到耦合核自旋上。交叉效应 DNP 转移的效率取决于两个电子自旋之间偶极-偶极耦合的大小。利用两个电子自旋之间的距离依赖性,我们可以感知 SDSL 肽的构型。利用 DNP 进行量子传感的一个显著优势是,这种方法可以在更高的磁场和魔角旋转条件下使用现有的仪器。这种方法还能观测更短的距离。总之,我们提出的方法为肽和聚合物研究中的结构分析和距离测量开辟了新的可能性,并与受人尊敬的科学家 Wayne Hubbell 教授提出的独创 SDSL 技术相结合。
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来源期刊
Applied Magnetic Resonance
Applied Magnetic Resonance 物理-光谱学
CiteScore
1.90
自引率
10.00%
发文量
59
审稿时长
2.3 months
期刊介绍: Applied Magnetic Resonance provides an international forum for the application of magnetic resonance in physics, chemistry, biology, medicine, geochemistry, ecology, engineering, and related fields. The contents include articles with a strong emphasis on new applications, and on new experimental methods. Additional features include book reviews and Letters to the Editor.
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