Simple, Scalable Proteomic Imaging for High-Dimensional Profiling of Intact Systems
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Chung_Simple, scalable.pdf
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Author(s)
Frosch, Matthew P.
Wedeen, Van J.
Seung, H. Sebastian
Murray, Evan
Cho, Jae Hun
Ku, Taeyun
Swaney, Justin Mark
Kim, Sung-Yon
Choi, Heejin
Park, Young-Gyun
Date Issued
December 2015
Journal
Cell
Publisher
Elsevier
Citation
Murray, Evan et al. “Simple, Scalable Proteomic Imaging for High-Dimensional Profiling of Intact Systems.” Cell 163.6 (2015): 1500–1514.
Version
Author's final manuscript
Abstract
Combined measurement of diverse molecular and anatomical traits that span multiple levels remains a major challenge in biology. Here, we introduce a simple method that enables proteomic imaging for scalable, integrated, high-dimensional phenotyping of both animal tissues and human clinical samples. This method, termed SWITCH, uniformly secures tissue architecture, native biomolecules, and antigenicity across an entire system by synchronizing the tissue preservation reaction. The heat- and chemical-resistant nature of the resulting framework permits multiple rounds (>20) of relabeling. We have performed 22 rounds of labeling of a single tissue with precise co-registration of multiple datasets. Furthermore, SWITCH synchronizes labeling reactions to improve probe penetration depth and uniformity of staining. With SWITCH, we performed combinatorial protein expression profiling of the human cortex and also interrogated the geometric structure of the fiber pathways in mouse brains. Such integrated high-dimensional information may accelerate our understanding of biological systems at multiple levels.
MIT Department
Massachusetts Institute of Technology. Institute for Medical Engineering & Science
Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences
Massachusetts Institute of Technology. Department of Chemical Engineering
Picower Institute for Learning and Memory
Terms of Use
Creative Commons Attribution-NonCommercial-NoDerivs License
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DOI of Published Version
https://doi.org/10.1016/j.cell.2015.11.025
