Diol Appended Quenchers for Fluorescein Boronic Acid

Research output: Contribution to journalArticle

Standard

Diol Appended Quenchers for Fluorescein Boronic Acid. / Elfeky, Souad; Flower, SE; Masumoto, N; D'Hooge, F; Labarthe, L; Chen, Wenbo; Len, C; James, TD; Fossey, John S.

In: Chemistry - An Asian Journal, Vol. 5, No. 3, 01.01.2010, p. 581-588.

Research output: Contribution to journalArticle

Harvard

Elfeky, S, Flower, SE, Masumoto, N, D'Hooge, F, Labarthe, L, Chen, W, Len, C, James, TD & Fossey, JS 2010, 'Diol Appended Quenchers for Fluorescein Boronic Acid', Chemistry - An Asian Journal, vol. 5, no. 3, pp. 581-588. https://doi.org/10.1002/asia.200900386

APA

Elfeky, S., Flower, SE., Masumoto, N., D'Hooge, F., Labarthe, L., Chen, W., Len, C., James, TD., & Fossey, J. S. (2010). Diol Appended Quenchers for Fluorescein Boronic Acid. Chemistry - An Asian Journal, 5(3), 581-588. https://doi.org/10.1002/asia.200900386

Vancouver

Elfeky S, Flower SE, Masumoto N, D'Hooge F, Labarthe L, Chen W et al. Diol Appended Quenchers for Fluorescein Boronic Acid. Chemistry - An Asian Journal. 2010 Jan 1;5(3):581-588. https://doi.org/10.1002/asia.200900386

Author

Elfeky, Souad ; Flower, SE ; Masumoto, N ; D'Hooge, F ; Labarthe, L ; Chen, Wenbo ; Len, C ; James, TD ; Fossey, John S. / Diol Appended Quenchers for Fluorescein Boronic Acid. In: Chemistry - An Asian Journal. 2010 ; Vol. 5, No. 3. pp. 581-588.

Bibtex

@article{d2f18f1fea044ecf98c47983052289b4,
title = "Diol Appended Quenchers for Fluorescein Boronic Acid",
abstract = "Fluorescein isothiocyanate is treated with 3-aminophenylboronic acid to provide a fluorescently tagged boronic acid derivative which is used to assess Forster resonance energy transfer (FRET) quenching upon boronate ester formation with a series of bespoke diol appended quenchers. Fluorescence spectroscopy comparison of quenching efficiency between treatment of fluorescein and its boronic acid appended congener with quencher appended diol reveals boronate ester formation (covalently linked) to be the more efficient regime and from the panel of quenchers which also included nucleosides.",
keywords = "nucleoside, receptor, fluorophore, boronic acid, quencher",
author = "Souad Elfeky and SE Flower and N Masumoto and F D'Hooge and L Labarthe and Wenbo Chen and C Len and TD James and Fossey, {John S.}",
year = "2010",
month = jan,
day = "1",
doi = "10.1002/asia.200900386",
language = "English",
volume = "5",
pages = "581--588",
journal = "Chemistry - An Asian Journal",
issn = "1861-4728",
publisher = "Wiley-VCH Verlag",
number = "3",

}

RIS

TY - JOUR

T1 - Diol Appended Quenchers for Fluorescein Boronic Acid

AU - Elfeky, Souad

AU - Flower, SE

AU - Masumoto, N

AU - D'Hooge, F

AU - Labarthe, L

AU - Chen, Wenbo

AU - Len, C

AU - James, TD

AU - Fossey, John S.

PY - 2010/1/1

Y1 - 2010/1/1

N2 - Fluorescein isothiocyanate is treated with 3-aminophenylboronic acid to provide a fluorescently tagged boronic acid derivative which is used to assess Forster resonance energy transfer (FRET) quenching upon boronate ester formation with a series of bespoke diol appended quenchers. Fluorescence spectroscopy comparison of quenching efficiency between treatment of fluorescein and its boronic acid appended congener with quencher appended diol reveals boronate ester formation (covalently linked) to be the more efficient regime and from the panel of quenchers which also included nucleosides.

AB - Fluorescein isothiocyanate is treated with 3-aminophenylboronic acid to provide a fluorescently tagged boronic acid derivative which is used to assess Forster resonance energy transfer (FRET) quenching upon boronate ester formation with a series of bespoke diol appended quenchers. Fluorescence spectroscopy comparison of quenching efficiency between treatment of fluorescein and its boronic acid appended congener with quencher appended diol reveals boronate ester formation (covalently linked) to be the more efficient regime and from the panel of quenchers which also included nucleosides.

KW - nucleoside

KW - receptor

KW - fluorophore

KW - boronic acid

KW - quencher

U2 - 10.1002/asia.200900386

DO - 10.1002/asia.200900386

M3 - Article

C2 - 20127786

VL - 5

SP - 581

EP - 588

JO - Chemistry - An Asian Journal

JF - Chemistry - An Asian Journal

SN - 1861-4728

IS - 3

ER -