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dc.contributor.authorTheile, Christopher S.
dc.contributor.authorChen, Guan-Yu
dc.contributor.authorBilate, Angelina M.
dc.contributor.authorDuarte, Joao N.
dc.contributor.authorAvalos, Ana M.
dc.contributor.authorFang, Tao
dc.contributor.authorBarberena, Roberto
dc.contributor.authorSato, Shuji
dc.contributor.authorPloegh, Hidde
dc.contributor.authorLi, Zeyang,S.M.Massachusetts Institute of Technology.
dc.date.accessioned2017-05-01T18:47:33Z
dc.date.available2017-05-01T18:47:33Z
dc.date.issued2015-09
dc.date.submitted2015-07
dc.identifier.issn1433-7851
dc.identifier.issn1521-3773
dc.identifier.urihttp://hdl.handle.net/1721.1/108551
dc.description.abstractThe site-specific modification of proteins with fluorophores can render a protein fluorescent without compromising its function. To avoid self-quenching from multiple fluorophores installed in close proximity, we used Holliday junctions to label proteins site-specifically. Holliday junctions enable modification with multiple fluorophores at reasonably precise spacing. We designed a Holliday junction with three of its four arms modified with a fluorophore of choice and the remaining arm equipped with a dibenzocyclooctyne substituent to render it reactive with an azide-modified fluorescent single-domain antibody fragment or an intact immunoglobulin produced in a sortase-catalyzed reaction. These fluorescent Holliday junctions improve fluorescence yields for both single-domain and full-sized antibodies without deleterious effects on antigen binding.en_US
dc.language.isoen_US
dc.publisherWiley Blackwellen_US
dc.relation.isversionofhttp://dx.doi.org/10.1002/anie.201505277en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleFluorophore-Conjugated Holliday Junctions for Generating Super-Bright Antibodies and Antibody Fragmentsen_US
dc.typeArticleen_US
dc.identifier.citationLi, Zeyang et al. “Fluorophore-Conjugated Holliday Junctions for Generating Super-Bright Antibodies and Antibody Fragments.” Angewandte Chemie International Edition 54.40 (2015): 11706–11710.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentWhitehead Institute for Biomedical Researchen_US
dc.contributor.mitauthorPloegh, Hidde
dc.relation.journalAngewandte Chemie International Editionen_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.orderedauthorsLi, Zeyang; Theile, Christopher S.; Chen, Guan-Yu; Bilate, Angelina M.; Duarte, Joao N.; Avalos, Ana M.; Fang, Tao; Barberena, Roberto; Sato, Shuji; Ploegh, Hidde L.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-1090-6071
mit.licenseOPEN_ACCESS_POLICYen_US


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