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dc.contributor.authorSaka, Sinem K
dc.contributor.authorWang, Yu
dc.contributor.authorKishi, Jocelyn Y
dc.contributor.authorZhu, Allen
dc.contributor.authorZeng, Yitian
dc.contributor.authorXie, Wenxin
dc.contributor.authorKirli, Koray
dc.contributor.authorYapp, Clarence
dc.contributor.authorCicconet, Marcelo
dc.contributor.authorBeliveau, Brian J
dc.contributor.authorLapan, Sylvain W
dc.contributor.authorYin, Siyuan
dc.contributor.authorLin, Millicent
dc.contributor.authorBoyden, Edward S
dc.contributor.authorKaeser, Pascal S
dc.contributor.authorPihan, German
dc.contributor.authorChurch, George M
dc.contributor.authorYin, Peng
dc.date.accessioned2021-10-27T20:35:20Z
dc.date.available2021-10-27T20:35:20Z
dc.date.issued2019
dc.identifier.urihttps://hdl.handle.net/1721.1/136430
dc.description.abstract© 2019, The Author(s), under exclusive licence to Springer Nature America, Inc. Spatial mapping of proteins in tissues is hindered by limitations in multiplexing, sensitivity and throughput. Here we report immunostaining with signal amplification by exchange reaction (Immuno-SABER), which achieves highly multiplexed signal amplification via DNA-barcoded antibodies and orthogonal DNA concatemers generated by primer exchange reaction (PER). SABER offers independently programmable signal amplification without in situ enzymatic reactions, and intrinsic scalability to rapidly amplify and visualize a large number of targets when combined with fast exchange cycles of fluorescent imager strands. We demonstrate 5- to 180-fold signal amplification in diverse samples (cultured cells, cryosections, formalin-fixed paraffin-embedded sections and whole-mount tissues), as well as simultaneous signal amplification for ten different proteins using standard equipment and workflows. We also combined SABER with expansion microscopy to enable rapid, multiplexed super-resolution tissue imaging. Immuno-SABER presents an effective and accessible platform for multiplexed and amplified imaging of proteins with high sensitivity and throughput.
dc.language.isoen
dc.publisherSpringer Science and Business Media LLC
dc.relation.isversionof10.1038/S41587-019-0207-Y
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/
dc.sourcePMC
dc.titleImmuno-SABER enables highly multiplexed and amplified protein imaging in tissues
dc.typeArticle
dc.contributor.departmentMassachusetts Institute of Technology. Media Laboratory
dc.relation.journalNature Biotechnology
dc.eprint.versionAuthor's final manuscript
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2021-03-11T18:50:05Z
dspace.orderedauthorsSaka, SK; Wang, Y; Kishi, JY; Zhu, A; Zeng, Y; Xie, W; Kirli, K; Yapp, C; Cicconet, M; Beliveau, BJ; Lapan, SW; Yin, S; Lin, M; Boyden, ES; Kaeser, PS; Pihan, G; Church, GM; Yin, P
dspace.date.submission2021-03-11T18:50:09Z
mit.journal.volume37
mit.journal.issue9
mit.licenseOPEN_ACCESS_POLICY
mit.metadata.statusAuthority Work and Publication Information Needed


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