dc.contributor.author | Valeri, Jacqueline A | |
dc.contributor.author | Collins, Katherine M | |
dc.contributor.author | Ramesh, Pradeep | |
dc.contributor.author | Alcantar, Miguel A | |
dc.contributor.author | Lepe, Bianca A | |
dc.contributor.author | Lu, Timothy K | |
dc.contributor.author | Camacho, Diogo M | |
dc.date.accessioned | 2021-10-27T20:04:59Z | |
dc.date.available | 2021-10-27T20:04:59Z | |
dc.date.issued | 2020 | |
dc.identifier.uri | https://hdl.handle.net/1721.1/134432 | |
dc.description.abstract | © 2020, The Author(s). While synthetic biology has revolutionized our approaches to medicine, agriculture, and energy, the design of completely novel biological circuit components beyond naturally-derived templates remains challenging due to poorly understood design rules. Toehold switches, which are programmable nucleic acid sensors, face an analogous design bottleneck; our limited understanding of how sequence impacts functionality often necessitates expensive, time-consuming screens to identify effective switches. Here, we introduce Sequence-based Toehold Optimization and Redesign Model (STORM) and Nucleic-Acid Speech (NuSpeak), two orthogonal and synergistic deep learning architectures to characterize and optimize toeholds. Applying techniques from computer vision and natural language processing, we ‘un-box’ our models using convolutional filters, attention maps, and in silico mutagenesis. Through transfer-learning, we redesign sub-optimal toehold sensors, even with sparse training data, experimentally validating their improved performance. This work provides sequence-to-function deep learning frameworks for toehold selection and design, augmenting our ability to construct potent biological circuit components and precision diagnostics. | |
dc.language.iso | en | |
dc.publisher | Springer Science and Business Media LLC | |
dc.relation.isversionof | 10.1038/s41467-020-18676-2 | |
dc.rights | Creative Commons Attribution 4.0 International license | |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
dc.source | Nature | |
dc.title | Sequence-to-function deep learning frameworks for engineered riboregulators | |
dc.type | Article | |
dc.contributor.department | Massachusetts Institute of Technology. Institute for Medical Engineering & Science | |
dc.contributor.department | Massachusetts Institute of Technology. Department of Biological Engineering | |
dc.contributor.department | Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences | |
dc.contributor.department | Massachusetts Institute of Technology. Research Laboratory of Electronics | |
dc.relation.journal | Nature Communications | |
dc.eprint.version | Final published version | |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
eprint.status | http://purl.org/eprint/status/PeerReviewed | |
dc.date.updated | 2021-01-28T19:43:16Z | |
dspace.orderedauthors | Valeri, JA; Collins, KM; Ramesh, P; Alcantar, MA; Lepe, BA; Lu, TK; Camacho, DM | |
dspace.date.submission | 2021-01-28T19:43:20Z | |
mit.journal.volume | 11 | |
mit.journal.issue | 1 | |
mit.license | PUBLISHER_CC | |
mit.metadata.status | Authority Work and Publication Information Needed | |