An approach to rapid distributed manufacturing of broad spectrum anti-viral griffithsin using cell-free systems to mitigate pandemics

dc.contributor.authorBorhani, Shayan G.
dc.contributor.authorLevine, Max Z.
dc.contributor.authorKrumpe, Lauren H.
dc.contributor.authorWilson, Jennifer
dc.contributor.authorHenrich, Curtis J.
dc.contributor.authorO’Keefe, Barry R.
dc.contributor.authorLo, Donald
dc.contributor.authorSittampalam, G. Sitta
dc.contributor.authorGodfrey, Alexander G.
dc.contributor.authorLunsford, R. Dwayne
dc.contributor.authorMangalampalli, Venkata
dc.contributor.authorTao, Dingyin
dc.contributor.authorLeClair, Christopher A.
dc.contributor.authorThole, Aaron
dc.contributor.authorFrey, Douglas
dc.contributor.authorSwartz, James
dc.contributor.authorRao, Govind
dc.date.accessioned2023-01-06T19:06:39Z
dc.date.available2023-01-06T19:06:39Z
dc.date.issued2022-12-20
dc.description.abstractThis study describes the cell-free biomanufacturing of a broad-spectrum antiviral protein, griffithsin (GRFT) such that it can be produced with consistent purity and potency in less than 24 hours. We demonstrate GRFT production using two independent cell-free systems, one plant and one microbial. Griffithsin purity and quality were verified using standard regulatory metrics. Efficacy was demonstrated in vitro against SARS-CoV-2 and HIV-1 and was nearly identical to that of GRFT expressed in vivo. The proposed production process is efficient and can be readily scaled up and deployed anywhere in the world where a viral pathogen might emerge. The current emergence of viral variants has resulted in frequent updating of existing vaccines and loss of efficacy for front-line monoclonal antibody therapies. Proteins such as GRFT with its efficacious and broad virus neutralizing capability provide a compelling pandemic mitigation strategy to promptly suppress viral emergence at the source of an outbreak.en_US
dc.description.sponsorshipMike Tolosa for helping generated a schematic of our distributed manufacturing platform. LenioBio for providing ALiCE Lysate. NIH/NCATS for material support. This project has been funded in whole or in part with Federal funds from the Frederick National Laboratory for Cancer Research, National Institutes of Health, under contract HHSN261200800001E. The content of this publication does not necessarily reflect the views or policies of the Department of Health and Human Services, nor does mention of trade names, commercial products or organizations imply endorsement by the US Governmenten_US
dc.description.urihttps://www.biorxiv.org/content/10.1101/2022.12.19.521044v1en_US
dc.format.extent21 pagesen_US
dc.genrejournal articlesen_US
dc.genrepreprintsen_US
dc.identifierdoi:10.13016/m2accg-dxxx
dc.identifier.urihttps://doi.org/10.1101/2022.12.19.521044
dc.identifier.urihttp://hdl.handle.net/11603/26586
dc.language.isoen_USen_US
dc.relation.isAvailableAtThe University of Maryland, Baltimore County (UMBC)
dc.relation.ispartofUMBC Center for Advanced Sensor Technology (CAST)
dc.relation.ispartofUMBC Faculty Collection
dc.relation.ispartofUMBC Student Collection
dc.relation.ispartofUMBC Mechanical Engineering Department
dc.rightsThis work was written as part of one of the author's official duties as an Employee of the United States Government and is therefore a work of the United States Government. In accordance with 17 U.S.C. 105, no copyright protection is available for such works under U.S. Law.en_US
dc.rightsPublic Domain Mark 1.0*
dc.rights.urihttp://creativecommons.org/publicdomain/mark/1.0/*
dc.titleAn approach to rapid distributed manufacturing of broad spectrum anti-viral griffithsin using cell-free systems to mitigate pandemicsen_US
dc.typeTexten_US
dcterms.creatorhttps://orcid.org/0000-0002-1229-8313en_US
dcterms.creatorhttps://orcid.org/0000-0002-1404-9783en_US
dcterms.creatorhttps://orcid.org/0000-0003-1123-1181en_US
dcterms.creatorhttps://orcid.org/0000-0001-6140-7582en_US

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