Robust collection and processing for label-free single voxel proteomics

• Published in: bioRxiv
• Main Authors: Kitata, Reta Birhanu, Velickovic, Marija, Xu, Zhangyang, Zhao, Rui, Scholten, David, Chu, Rosalie K, Orton, Daniel J, Chrisler, William B, Mathews, Jeremy V, Piehowski, Paul D, Liu, Tao, Smith, Richard D, Liu, Huiping, Wasserfall, Clive H, Tsai, Chia-Feng, Shi, Tujin
• Format: Journal Article
• Language: English
• Published: United States 15.08.2023
• DOI: 10.1101/2023.08.14.553333
• ISSN: 2692-8205

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 important tissue heterogeneity, which make it impossible for proteome mapping of tissue microenvironment. Here we report an integrated wet collection of single tissue voxel 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 tissue voxel dissected by LCM into the PCR tube cap and MS-compatible surfactant-assisted one-pot voxel processing in the collection cap. This convenient method allows reproducible label-free quantification of ∼900 and ∼4,600 proteins for single voxel from fresh frozen human spleen tissue at 20 μm × 20 μm × 10 μm (close to single cells) and 200 μm × 200 μm × 10 μm (∼100 cells), respectively. 100s-1000s of protein signatures with differential expression levels were identified to be spatially resolved between spleen red and white pulp regions depending on the voxel size. Region-specific signaling pathways were enriched from single voxel proteomics data. Antibody-based CODEX imaging was used to validate label-free MS quantitation for single voxel analysis. The wcSOP-MS method paves the way for routine robust single voxel proteomics and spatial proteomics.