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dc.contributor.authorTruex, Nicholas
dc.contributor.authorHolden, Rebecca Lynn
dc.contributor.authorWang, Bin-You
dc.contributor.authorChen, Pu-Guang
dc.contributor.authorHanna, Stephanie
dc.contributor.authorHu, Zhuting
dc.contributor.authorShetty, Keerthi
dc.contributor.authorOlive, Oriol
dc.contributor.authorNeuberg, Donna
dc.contributor.authorHacohen, Nir
dc.contributor.authorKeskin, Derin B.
dc.contributor.authorOtt, Patrick A.
dc.contributor.authorWu, Catherine J.
dc.contributor.authorPentelute, Bradley L.
dc.date.accessioned2020-10-27T22:14:12Z
dc.date.available2020-10-27T22:14:12Z
dc.date.issued2020-01
dc.date.submitted2019-06
dc.identifier.issn2045-2322
dc.identifier.urihttps://hdl.handle.net/1721.1/128223
dc.description.abstractHigh-throughput genome sequencing and computation have enabled rapid identification of targets for personalized medicine, including cancer vaccines. Synthetic peptides are an established mode of cancer vaccine delivery, but generating the peptides for each patient in a rapid and affordable fashion remains difficult. High-throughput peptide synthesis technology is therefore urgently needed for patient-specific cancer vaccines to succeed in the clinic. Previously, we developed automated flow peptide synthesis technology that greatly accelerates the production of synthetic peptides. Herein, we show that this technology permits the synthesis of high-quality peptides for personalized medicine. Automated flow synthesis produces 30-mer peptides in less than 35 minutes and 15- to 16-mer peptides in less than 20 minutes. The purity of these peptides is comparable with or higher than the purity of peptides produced by other methods. This work illustrates how automated flow synthesis technology can enable customized peptide therapies by accelerating synthesis and increasing purity. We envision that implementing this technology in clinical settings will greatly increase capacity to generate clinical-grade peptides on demand, which is a key step in reaching the full potential of personalized vaccines for the treatment of cancer and other diseases.en_US
dc.description.sponsorshipNational Science Foundation (Grant 1122374)en_US
dc.description.sponsorshipNational Institutes of Health (Grants R21-CA216772-01A1 and NCI-1RO1CA155010-02)en_US
dc.description.sponsorshipNational Cancer Institute (Grants R21 CA216772-01A1 and SPORE-2P50CA101942-11A1)en_US
dc.description.sponsorshipNHLBI (Grant 5R01HL103532-03)en_US
dc.language.isoen
dc.publisherSpringer Science and Business Media LLCen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/s41598-019-56943-5en_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceScientific Reportsen_US
dc.titleAutomated Flow Synthesis of Tumor Neoantigen Peptides for Personalized Immunotherapyen_US
dc.typeArticleen_US
dc.identifier.citationTruex, Nicholas L. "Automated Flow Synthesis of Tumor Neoantigen Peptides for Personalized Immunotherapy." Scientific Reports 10, 1 (Janauary 2020): 723 © 2020 The Author(s)en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.relation.journalScientific Reportsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2020-09-21T13:38:59Z
dspace.date.submission2020-09-21T13:39:01Z
mit.journal.volume10en_US
mit.journal.issue1en_US
mit.licensePUBLISHER_CC
mit.metadata.statusComplete


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