High-dimensional imaging using combinatorial channel multiplexing and deep learning

被引:0
|
作者
Ben-Uri, Raz [1 ]
Ben Shabat, Lior [1 ,2 ]
Shainshein, Dana [1 ]
Bar-Tal, Omer [2 ]
Bussi, Yuval [1 ,2 ]
Maimon, Noa [1 ]
Haran, Tal Keidar [1 ,3 ]
Milo, Idan [1 ]
Goliand, Inna [4 ]
Addadi, Yoseph [4 ]
Salame, Tomer Meir [4 ]
Rochwarger, Alexander [5 ,6 ]
Schuerch, Christian M. [5 ,6 ,7 ]
Bagon, Shai [2 ]
Elhanani, Ofer [1 ]
Keren, Leeat [1 ]
机构
[1] Weizmann Inst Sci, Dept Mol Cell Biol, Rehovot, Israel
[2] Weizmann Inst Sci, Dept Math & Comp Sci, Rehovot, Israel
[3] HADASSAH MED CTR, DEPT PATHOL, JERUSALEM, Israel
[4] Weizmann Inst Sci, Life Sci Core Facil, Rehovot, Israel
[5] Univ Hosp, Dept Pathol & Neuropathol, Tubingen, Germany
[6] Comprehens Canc Ctr Tubingen, Tubingen, Germany
[7] Univ Tubingen, Cluster Excellence iFIT EXC 2180 Image Guided & Fu, Tubingen, Germany
基金
欧盟地平线“2020”; 以色列科学基金会; 欧洲研究理事会;
关键词
IMMUNOHISTOCHEMISTRY; CELLS;
D O I
10.1038/s41587-025-02585-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Understanding tissue structure and function requires tools that quantify the expression of multiple proteins at single-cell resolution while preserving spatial information. Current imaging technologies use a separate channel for each protein, limiting throughput and scalability. Here, we present combinatorial multiplexing (CombPlex), a combinatorial staining platform coupled with an algorithmic framework to exponentially increase the number of measured proteins. Every protein can be imaged in several channels and every channel contains agglomerated images of several proteins. These combinatorically compressed images are then decompressed to individual protein images using deep learning. We achieve accurate reconstruction when compressing the stains of 22 proteins to five imaging channels. We demonstrate the approach both in fluorescence microscopy and in mass-based imaging and show successful application across multiple tissues and cancer types. CombPlex can escalate the number of proteins measured by any imaging modality, without the need for specialized instrumentation.
引用
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页数:23
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