CODEX multiplexed tissue imaging with DNA-conjugated antibodies
Top Cited Papers
- 2 July 2021
- journal article
- research article
- Published by Springer Nature in Nature Protocols
- Vol. 16 (8) , 3802-3835
Abstract
Advances in multiplexed imaging technologies have drastically improved our ability to characterize healthy and diseased tissues at the single-cell level. Co-detection by indexing (CODEX) relies on DNA-conjugated antibodies and the cyclic addition and removal of complementary fluorescently labeled DNA probes and has been used so far to simultaneously visualize up to 60 markers in situ. CODEX enables a deep view into the single-cell spatial relationships in tissues and is intended to spur discovery in developmental biology, disease and therapeutic design. Herein, we provide optimized protocols for conjugating purified antibodies to DNA oligonucleotides, validating the conjugation by CODEX staining and executing the CODEX multicycle imaging procedure for both formalin-fixed, paraffin-embedded (FFPE) and fresh-frozen tissues. In addition, we describe basic image processing and data analysis procedures. We apply this approach to an FFPE human tonsil multicycle experiment. The hands-on experimental time for antibody conjugation is ~4.5 h, validation of DNA-conjugated antibodies with CODEX staining takes ~6.5 h and preparation for a CODEX multicycle experiment takes ~8 h. The multicycle imaging and data analysis time depends on the tissue size, number of markers in the panel and computational complexity.Keywords
Funding Information
- U.S. Department of Health & Human Services | NIH | Office of Extramural Research, National Institutes of Health (5P01HL10879707)
- U.S. Department of Health & Human Services | National Institutes of Health (5R01GM10983604, 5R33CA18365403, 5U01AI101984-07, 5UH2AR06767604, 5R01CA19665703, 5U54CA20997103, 5F99CA212231-02, 1F32CA233203-01, 5U01AI140498-02, 1U54HG010426-01, 5U19AI100627-07, 1R01HL120724-01A1, R33CA183692, R01HL128173-04, 5P01AI131374-02, 5UG3DK114937-02, 1U19AI135976-01, IDIQ17X149, 1U2CCA233238-01, 1U2CCA233195-01, AR007422, CA233203, T32CA196585)
- U.S. Department of War (W81XWH-14-1-0180, W81XWH-12-1-0591)
- U.S. Department of Health & Human Services | U.S. Food and Drug Administration (HHSF223201610018C, DSTL/AGR/00980/01)
- Cancer Research UK (C27165/A29073)
- Bill and Melinda Gates Foundation (OPP1113682)
- Silicon Valley Community Foundation (2017-175329, 2017-177799-5022)
- Pfizer (123214)
- Celgene (133826, 133826)
- American Cancer Society (PF-20-032-01-CSM)
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (P300PB_171189, P400PM_183915)
This publication has 39 references indexed in Scilit:
- Highly multiplexed tissue imaging using repeated oligonucleotide exchange reactionEuropean Journal of Immunology, 2021
- Coordinated Cellular Neighborhoods Orchestrate Antitumoral Immunity at the Colorectal Cancer Invasive FrontCell, 2020
- Multiplexed protein maps link subcellular organization to cellular statesScience, 2018
- Deep Profiling of Mouse Splenic Architecture with CODEX Multiplexed ImagingCell, 2018
- Highly multiplexed immunofluorescence imaging of human tissues and tumors using t-CyCIF and conventional optical microscopeseLife, 2018
- Rapid Sequential in Situ Multiplexing with DNA Exchange Imaging in Neuronal Cells and TissuesNano Letters, 2017
- DNA-barcoded labeling probes for highly multiplexed Exchange-PAINT imagingChemical Science, 2017
- Highly multiplexed single-cell analysis of formalin-fixed, paraffin-embedded cancer tissueProceedings of the National Academy of Sciences, 2013
- A colorful future of quantitative pathology: validation of Vectra technology using chromogenic multiplexed immunohistochemistry and prostate tissue microarraysHuman Pathology, 2013
- Analyzing proteome topology and function by automated multidimensional fluorescence microscopyNature Biotechnology, 2006