Ward, Jonathan Stuart, De Palo, Alice, Aucott, Benjamin James et al. (3 more authors) (2019) A Biotin-Conjugated photo-activated CO-Releasing Molecule (BiotinCORM): Efficient CO-release from an avidin-BiotinCORM protein adduct. Dalton Transactions. ISSN 1477-9234
Abstract
Biotinylated pharmaceuticals are of great interest due to the strong interactions between biotinyl-functionality and streptavidin/avidin, which opens up avenues for efficient targeting and localisation. Three new carbon monoxide-releasing molecules (CO-RMs) have been synthesised and characterised using chemical and biological analysis. An alkyne-containing CO-RM 2 was found to be toxic to RAW 264.7 murine macrophages; and thus therapeutically viable CO-RM 1 was employed as the alkyne precursor for [3+2] cycloaddition chemistry enabling a new acid-containing CO-RM 4 and biotin-bioconugate-CO-RM (BiotinCORM 5) to be prepared. CO-RM 4 showed significantly improved solubility and BiotinCORM 5 acts as a photo-CO-RM. We have found that an avidin-CORM adduct of 5 is a CO-releasing protein, releasing CO on irradiation with light (400 nm). The avidin-biotinCORM adduct of 5 was found to have a binding energy of 10 kcal mol−1. BiotinCORM 5 is the first example of a biotin conjugate CO-RM.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | © The Royal Society of Chemistry 2019. This is an author-produced version of the published paper. Uploaded in accordance with the publisher’s self-archiving policy. Further copying may not be permitted; contact the publisher for details. |
Dates: |
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Institution: | The University of York |
Academic Units: | The University of York > Faculty of Sciences (York) > Chemistry (York) The University of York > Faculty of Sciences (York) > Biology (York) |
Depositing User: | Pure (York) |
Date Deposited: | 16 Dec 2019 10:20 |
Last Modified: | 16 Oct 2024 15:58 |
Published Version: | https://doi.org/10.1039/C9DT03429C |
Status: | Published online |
Refereed: | Yes |
Identification Number: | 10.1039/C9DT03429C |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:154593 |
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