Spatial proteomics of single cells and organelles on tissue slides using filter-aided expansion proteomics

Zhen Dong(Westlake University), Wenhao Jiang(Westlake University), Chunlong Wu(Westlake University), Ting Chen(Zhejiang University), Jiayi Chen(Westlake University), Xuan Ding(Westlake University), Shu Zheng(Zhejiang University), Kiryl D. Piatkevich(Westlake University), Yi Zhu(Westlake University), Tiannan Guo(Westlake University)
Nature Communications
October 30, 2024
Cited by 45Open Access
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Abstract

Hydrogel-based tissue expansion combined with mass spectrometry (MS) offers an emerging spatial proteomics approach. Here, we present a filter-aided expansion proteomics (FAXP) strategy for spatial proteomics analysis of archived formalin-fixed paraffin-embedded (FFPE) specimens. Compared to our previous ProteomEx method, FAXP employed a customized tip device to enhance both the stability and throughput of sample preparation, thus guaranteeing the reproducibility and robustness of the workflow. FAXP achieved a 14.5-fold increase in volumetric resolution. It generated over 8 times higher peptide yield and a 255% rise in protein identifications while reducing sample preparation time by 50%. We also demonstrated the applicability of FAXP using human colorectal FFPE tissue samples. Furthermore, for the first time, we achieved bona fide single-subcellular proteomics under image guidance by integrating FAXP with laser capture microdissection. Hydrogel-based tissue expansion proteomics represents an emerging spatial proteomics approach. Here, the authors develop the filter-aided expansion proteomics (FAXP) strategy, enabling proteomic analysis of single cells and nuclei in formalin-fixed paraffin-embedded (FFPE) tissue sections.


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