An approach to rapid distributed manufacturing of broad spectrum anti-viral griffithsin using cell-free systems to mitigate pandemics
dc.contributor.author | Borhani, Shayan G. | |
dc.contributor.author | Levine, Max Z. | |
dc.contributor.author | Krumpe, Lauren H. | |
dc.contributor.author | Wilson, Jennifer | |
dc.contributor.author | Henrich, Curtis J. | |
dc.contributor.author | O’Keefe, Barry R. | |
dc.contributor.author | Lo, Donald | |
dc.contributor.author | Sittampalam, G. Sitta | |
dc.contributor.author | Godfrey, Alexander G. | |
dc.contributor.author | Lunsford, R. Dwayne | |
dc.contributor.author | Mangalampalli, Venkata | |
dc.contributor.author | Tao, Dingyin | |
dc.contributor.author | LeClair, Christopher A. | |
dc.contributor.author | Thole, Aaron | |
dc.contributor.author | Frey, Douglas | |
dc.contributor.author | Swartz, James | |
dc.contributor.author | Rao, Govind | |
dc.date.accessioned | 2023-01-06T19:06:39Z | |
dc.date.available | 2023-01-06T19:06:39Z | |
dc.date.issued | 2022-12-20 | |
dc.description.abstract | This 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.sponsorship | Mike 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 Government | en_US |
dc.description.uri | https://www.biorxiv.org/content/10.1101/2022.12.19.521044v1 | en_US |
dc.format.extent | 21 pages | en_US |
dc.genre | journal articles | en_US |
dc.genre | preprints | en_US |
dc.identifier | doi:10.13016/m2accg-dxxx | |
dc.identifier.uri | https://doi.org/10.1101/2022.12.19.521044 | |
dc.identifier.uri | http://hdl.handle.net/11603/26586 | |
dc.language.iso | en_US | en_US |
dc.relation.isAvailableAt | The University of Maryland, Baltimore County (UMBC) | |
dc.relation.ispartof | UMBC Center for Advanced Sensor Technology (CAST) | |
dc.relation.ispartof | UMBC Faculty Collection | |
dc.relation.ispartof | UMBC Student Collection | |
dc.relation.ispartof | UMBC Mechanical Engineering Department | |
dc.rights | This 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.rights | Public Domain Mark 1.0 | * |
dc.rights.uri | http://creativecommons.org/publicdomain/mark/1.0/ | * |
dc.title | An approach to rapid distributed manufacturing of broad spectrum anti-viral griffithsin using cell-free systems to mitigate pandemics | en_US |
dc.type | Text | en_US |
dcterms.creator | https://orcid.org/0000-0002-1229-8313 | en_US |
dcterms.creator | https://orcid.org/0000-0002-1404-9783 | en_US |
dcterms.creator | https://orcid.org/0000-0003-1123-1181 | en_US |
dcterms.creator | https://orcid.org/0000-0001-6140-7582 | en_US |
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