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

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A biotin-conjugated photo-activated CO-releasing molecule (biotinCORM): efficient CO-release from an avidin–biotinCORM protein adduct. / Ward, Jonathan S.; Palo, Alice De; Aucott, Benjamin J. et al.
In: Dalton Transactions, Vol. 48, No. 43, 21.11.2019, p. 16233-16241.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Ward, JS, Palo, AD, Aucott, BJ, Moir, JWB, Lynam, JM & Fairlamb, IJS 2019, 'A biotin-conjugated photo-activated CO-releasing molecule (biotinCORM): efficient CO-release from an avidin–biotinCORM protein adduct', Dalton Transactions, vol. 48, no. 43, pp. 16233-16241. https://doi.org/10.1039/C9DT03429C

APA

Ward, J. S., Palo, A. D., Aucott, B. J., Moir, J. W. B., Lynam, J. M., & Fairlamb, I. J. S. (2019). A biotin-conjugated photo-activated CO-releasing molecule (biotinCORM): efficient CO-release from an avidin–biotinCORM protein adduct. Dalton Transactions, 48(43), 16233-16241. https://doi.org/10.1039/C9DT03429C

Vancouver

Ward JS, Palo AD, Aucott BJ, Moir JWB, Lynam JM, Fairlamb IJS. A biotin-conjugated photo-activated CO-releasing molecule (biotinCORM): efficient CO-release from an avidin–biotinCORM protein adduct. Dalton Transactions. 2019 Nov 21;48(43):16233-16241. Epub 2019 Oct 10. doi: 10.1039/C9DT03429C

Author

Ward, Jonathan S. ; Palo, Alice De ; Aucott, Benjamin J. et al. / A biotin-conjugated photo-activated CO-releasing molecule (biotinCORM) : efficient CO-release from an avidin–biotinCORM protein adduct. In: Dalton Transactions. 2019 ; Vol. 48, No. 43. pp. 16233-16241.

Bibtex

@article{4e31da5c8a744117ba8793cf09d781a5,
title = "A biotin-conjugated photo-activated CO-releasing molecule (biotinCORM): efficient CO-release from an avidin–biotinCORM protein adduct",
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.",
author = "Ward, {Jonathan S.} and Palo, {Alice De} and Aucott, {Benjamin J.} and Moir, {James W. B.} and Lynam, {Jason M.} and Fairlamb, {Ian J. S.}",
year = "2019",
month = nov,
day = "21",
doi = "10.1039/C9DT03429C",
language = "English",
volume = "48",
pages = "16233--16241",
journal = "Dalton Transactions",
issn = "1477-9226",
publisher = "Royal Society of Chemistry",
number = "43",

}

RIS

TY - JOUR

T1 - A biotin-conjugated photo-activated CO-releasing molecule (biotinCORM)

T2 - efficient CO-release from an avidin–biotinCORM protein adduct

AU - Ward, Jonathan S.

AU - Palo, Alice De

AU - Aucott, Benjamin J.

AU - Moir, James W. B.

AU - Lynam, Jason M.

AU - Fairlamb, Ian J. S.

PY - 2019/11/21

Y1 - 2019/11/21

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.

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.

U2 - 10.1039/C9DT03429C

DO - 10.1039/C9DT03429C

M3 - Journal article

VL - 48

SP - 16233

EP - 16241

JO - Dalton Transactions

JF - Dalton Transactions

SN - 1477-9226

IS - 43

ER -