A Biotin-Conjugated photo-activated CO-Releasing Molecule (BiotinCORM): Efficient CO-release from an avidin-BiotinCORM protein adduct

TY - JOUR

T1 - A Biotin-Conjugated photo-activated CO-Releasing Molecule (BiotinCORM): Efficient CO-release from an avidin-BiotinCORM protein adduct

AU - Ward, Jonathan Stuart

AU - De Palo, Alice

AU - Aucott, Benjamin James

AU - Moir, James

AU - Lynam, Jason Martin

AU - Fairlamb, Ian James Stewart

N1 - © 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.

PY - 2019/10/10

Y1 - 2019/10/10

N2 - 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.

AB - 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.

U2 - 10.1039/C9DT03429C

DO - 10.1039/C9DT03429C

M3 - Article

SN - 1477-9234

JO - Dalton Transactions

JF - Dalton Transactions

ER -