Show simple item record

dc.contributor.authorAdamala, Katarzyna
dc.contributor.authorMartin Alarcon, Daniel Alberto
dc.contributor.authorBoyden, Edward
dc.date.accessioned2017-06-16T18:15:39Z
dc.date.available2017-06-16T18:15:39Z
dc.date.issued2016-04
dc.date.submitted2015-09
dc.identifier.issn0027-8424
dc.identifier.issn1091-6490
dc.identifier.urihttp://hdl.handle.net/1721.1/109966
dc.description.abstractThe ability to monitor and perturb RNAs in living cells would benefit greatly from a modular protein architecture that targets unmodified RNA sequences in a programmable way. We report that the RNA-binding protein PumHD (Pumilio homology domain), which has been widely used in native and modified form for targeting RNA, can be engineered to yield a set of four canonical protein modules, each of which targets one RNA base. These modules (which we call Pumby, for Pumilio-based assembly) can be concatenated in chains of varying composition and length, to bind desired target RNAs. The specificity of such Pumby–RNA interactions was high, with undetectable binding of a Pumby chain to RNA sequences that bear three or more mismatches from the target sequence. We validate that the Pumby architecture can perform RNA-directed protein assembly and enhancement of translation of RNAs. We further demonstrate a new use of such RNA-binding proteins, measurement of RNA translation in living cells. Pumby may prove useful for many applications in the measurement, manipulation, and biotechnological utilization of unmodified RNAs in intact cells and systems.en_US
dc.description.sponsorshipUnited States. National Institutes of Health (1R01NS075421)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (1344219)en_US
dc.description.sponsorshipUnited States. National Institutes of Health (1U01MH106011)en_US
dc.description.sponsorshipUnited States. National Institutes of Health (1R01MH103910)en_US
dc.description.sponsorshipUnited States. National Institutes of Health (1DP1NS087724)en_US
dc.language.isoen_US
dc.publisherNational Academy of Sciences (U.S.)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1073/pnas.1519368113en_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.sourcePNASen_US
dc.titleProgrammable RNA-binding protein composed of repeats of a single modular uniten_US
dc.typeArticleen_US
dc.identifier.citationAdamala, Katarzyna P.; Martin-Alarcon, Daniel A. and Boyden, Edward S. “Programmable RNA-Binding Protein Composed of Repeats of a Single Modular Unit.” Proceedings of the National Academy of Sciences 113, no. 19 (April 2016): E2579–E2588 © 2016 National Academy of Sciencesen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciencesen_US
dc.contributor.departmentMassachusetts Institute of Technology. Media Laboratoryen_US
dc.contributor.mitauthorAdamala, Katarzyna
dc.contributor.mitauthorMartin Alarcon, Daniel Alberto
dc.contributor.mitauthorBoyden, Edward
dc.relation.journalProceedings of the National Academy of Sciencesen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsAdamala, Katarzyna P.; Martin-Alarcon, Daniel A.; Boyden, Edward S.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0003-0547-8129
dc.identifier.orcidhttps://orcid.org/0000-0002-0419-3351
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record