In-Cell DEER Spectroscopy of Nanodisc-Delivered Membrane Proteins in Living Cell Membranes

IF 8.5 Q1 CHEMISTRY, MULTIDISCIPLINARY JACS Au Pub Date : 2024-09-24 DOI:10.1021/jacsau.4c0070210.1021/jacsau.4c00702
Chu-Chun Cheng, Ruei-Fong Tsai, Che-Kai Lin, Kui-Thong Tan, Vidmantas Kalendra, Mantas Simenas, Chun-Wei Lin* and Yun-Wei Chiang*, 
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Abstract

Membrane proteins are integral to numerous cellular processes, yet their conformational dynamics in native environments remains difficult to study. This study introduces a nanodelivery method using nanodiscs to transport spin-labeled membrane proteins into the membranes of living cells, enabling direct in-cell double electron–electron resonance (DEER) spectroscopy measurements. We investigated the membrane protein BsYetJ, incorporating spin labels at key positions to monitor conformational changes. Our findings demonstrate successful delivery and high-quality DEER data for BsYetJ in both Gram-negative E. coli and Gram-positive B. subtilis membranes. The delivered BsYetJ retains its ability to transport calcium ions. DEER analysis reveals distinct conformational states of BsYetJ in different membrane environments, highlighting the influence of lipid composition on the protein structure. This nanodelivery method overcomes traditional limitations, enabling the study of membrane proteins in more physiologically relevant conditions.

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活细胞膜中纳米盘递送膜蛋白的细胞内 DEER 光谱分析
膜蛋白是众多细胞过程不可或缺的组成部分,但它们在原生环境中的构象动力学仍然难以研究。本研究介绍了一种利用纳米盘将自旋标记的膜蛋白输送到活细胞膜中的纳米输送方法,从而可以直接在细胞内进行双电子电子共振(DEER)光谱测量。我们研究了膜蛋白 BsYetJ,在关键位置加入了自旋标签,以监测构象变化。我们的研究结果表明,BsYetJ 在革兰氏阴性的大肠杆菌和革兰氏阳性的枯草杆菌膜中都能成功传递并获得高质量的 DEER 数据。输送的 BsYetJ 保留了其运输钙离子的能力。DEER 分析揭示了 BsYetJ 在不同膜环境中的不同构象状态,突出了脂质成分对蛋白质结构的影响。这种纳米递送方法克服了传统的局限性,能够在更贴近生理的条件下研究膜蛋白。
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