Kitata Reta Birhanu, Velickovic Marija, Xu Zhangyang, Zhao Rui, Scholten David, Chu Rosalie K, Orton Daniel J, Chrisler William B, Zhang Tong, Mathews Jeremy V, Bumgarner Benjamin M, Gursel Demirkan B, Moore Ronald J, Piehowski Paul D, Liu Tao, Smith Richard D, Liu Huiping, Wasserfall Clive H, Tsai Chia-Feng, Shi Tujin
Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA, 99354, USA.
Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, WA, 99354, USA.
Nat Commun. 2025 Jan 13;16(1):547. doi: 10.1038/s41467-024-54643-x.
With advanced mass spectrometry (MS)-based proteomics, genome-scale proteome coverage can be achieved from bulk tissues. However, such bulk measurement lacks spatial resolution and obscures tissue heterogeneity, precluding proteome mapping of tissue microenvironment. Here we report an integrated wet collection of single microscale tissue voxels and Surfactant-assisted One-Pot voxel processing method termed wcSOP for robust label-free single voxel proteomics. wcSOP capitalizes on buffer droplet-assisted wet collection of single voxels dissected by LCM to the tube cap and SOP voxel processing in the same collection cap. This method enables reproducible, label-free quantification of approximately 900 and 4600 proteins for single voxels at 20 µm × 20 µm × 10 µm (1 cell region) and 200 µm × 200 µm × 10 µm (100 cell region) from fresh frozen human spleen tissue, respectively. It can reveal spatially resolved protein signatures and region-specific signaling pathways. Furthermore, wcSOP-MS is demonstrated to be broadly applicable for OCT-embedded and FFPE human archived tissues as well as for small-scale 2D proteome mapping of tissues at high spatial resolutions. wcSOP-MS may pave the way for routine robust single voxel proteomics and spatial proteomics.
借助基于先进质谱(MS)的蛋白质组学技术,可以从大块组织中实现基因组规模的蛋白质组覆盖。然而,这种整体测量缺乏空间分辨率,掩盖了组织异质性,从而无法对组织微环境进行蛋白质组图谱绘制。在此,我们报告了一种集成的湿式单细胞组织体素收集方法以及一种称为wcSOP的表面活性剂辅助单一体素处理方法,用于可靠的无标记单一体素蛋白质组学研究。wcSOP利用缓冲液滴辅助湿式收集通过激光捕获显微切割(LCM)切割到管帽中的单一体素,并在同一收集帽中进行SOP体素处理。该方法能够对新鲜冷冻的人脾脏组织中20 µm×20 µm×10 µm(约1个细胞区域)和200 µm×200 µm×10 µm(约100个细胞区域)的单一体素分别进行约900种和4600种蛋白质的可重复、无标记定量分析。它可以揭示空间分辨的蛋白质特征和区域特异性信号通路。此外,wcSOP-MS被证明广泛适用于OCT包埋和福尔马林固定石蜡包埋(FFPE)的人类存档组织,以及高空间分辨率下组织的小规模二维蛋白质组图谱绘制。wcSOP-MS可能为常规的可靠单一体素蛋白质组学和空间蛋白质组学铺平道路。