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A biotin-conjugated photo-activated CO-releasing molecule (biotinCORM): efficient CO-release from an avidin–biotinCORM protein adduct.

Authors :
Ward, Jonathan S.
De Palo, Alice
Aucott, Benjamin J.
Moir, James W. B.
Lynam, Jason M.
Fairlamb, Ian J. S.
Source :
Dalton Transactions: An International Journal of Inorganic Chemistry; 11/21/2019, Vol. 48 Issue 43, p16233-16241, 9p
Publication Year :
2019

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<superscript>−1</superscript>. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14779226
Volume :
48
Issue :
43
Database :
Complementary Index
Journal :
Dalton Transactions: An International Journal of Inorganic Chemistry
Publication Type :
Academic Journal
Accession number :
139509188
Full Text :
https://doi.org/10.1039/c9dt03429c