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dc.contributor.authorDeerinck, Thomas J.
dc.contributor.authorSancak, Yasemin
dc.contributor.authorPoulos, Thomas L.
dc.contributor.authorMootha, Vamsi K.
dc.contributor.authorSosinsky, Gina E.
dc.contributor.authorEllisman, Mark H.
dc.contributor.authorMartell, Jeffrey Daniel
dc.contributor.authorTing, Alice Y.
dc.date.accessioned2015-03-03T15:25:56Z
dc.date.available2015-03-03T15:25:56Z
dc.date.issued2012-10
dc.date.submitted2012-06
dc.identifier.issn1087-0156
dc.identifier.issn1546-1696
dc.identifier.urihttp://hdl.handle.net/1721.1/95743
dc.description.abstractElectron microscopy (EM) is the standard method for imaging cellular structures with nanometer resolution, but existing genetic tags are inactive in most cellular compartments[superscript 1] or require light and can be difficult to use[superscript 2]. Here we report the development of 'APEX', a genetically encodable EM tag that is active in all cellular compartments and does not require light. APEX is a monomeric 28-kDa peroxidase that withstands strong EM fixation to give excellent ultrastructural preservation. We demonstrate the utility of APEX for high-resolution EM imaging of a variety of mammalian organelles and specific proteins using a simple and robust labeling procedure. We also fused APEX to the N or C terminus of the mitochondrial calcium uniporter (MCU), a recently identified channel whose topology is disputed[superscript 3, 4]. These fusions give EM contrast exclusively in the mitochondrial matrix, suggesting that both the N and C termini of MCU face the matrix. Because APEX staining is not dependent on light activation, APEX should make EM imaging of any cellular protein straightforward, regardless of the size or thickness of the specimen.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant DP1 OD003961)en_US
dc.description.sponsorshipNational Science Foundation (U.S.). Graduate Research Fellowship Programen_US
dc.description.sponsorshipUnited States. Dept. of Defense (National Defense Science and Engineering Graduate (NDSEG) Fellowships)en_US
dc.language.isoen_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/nbt.2375en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourcePMCen_US
dc.titleEngineered ascorbate peroxidase as a genetically encoded reporter for electron microscopyen_US
dc.typeArticleen_US
dc.identifier.citationMartell, Jeffrey D, Thomas J Deerinck, Yasemin Sancak, Thomas L Poulos, Vamsi K Mootha, Gina E Sosinsky, Mark H Ellisman, and Alice Y Ting. “Engineered Ascorbate Peroxidase as a Genetically Encoded Reporter for Electron Microscopy.” Nature Biotechnology 30, no. 11 (October 21, 2012): 1143–1148.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.mitauthorMartell, Jeffrey Danielen_US
dc.contributor.mitauthorTing, Alice Y.en_US
dc.relation.journalNature Biotechnologyen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsMartell, Jeffrey D; Deerinck, Thomas J; Sancak, Yasemin; Poulos, Thomas L; Mootha, Vamsi K; Sosinsky, Gina E; Ellisman, Mark H; Ting, Alice Yen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-8277-5226
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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