Journal article

Dual-fluorescence pH probe for bio-labelling


Authors listRichter, C; Schneider, C; Quick, MT; Volz, P; Mahrwald, R; Hughes, J; Dick, B; Alexiev, U; Ernsting, NP

Publication year2015

Pages30590-30597

JournalPhysical Chemistry Chemical Physics

Volume number17

Issue number45

ISSN1463-9076

Open access statusHybrid

DOI Linkhttps://doi.org/10.1039/c5cp05454k

PublisherRoyal Society of Chemistry


Abstract
Although seminaphtorhodafluor (SNARF) dyes are already widely used to measure pH in cells and at biofilms, their synthesis has low yield and results in an unspecific position of a carboxy-group. The separation of 5'-and 6'-carboxy-SNARF reveals a pK(a) difference of 0.15, calling into question pH measurements with the (commercially available) mixture. Here we replace the bulky external dicarboxyphenyl ring with a propionate group and evaluate the spectral properties of the new derivative. Proceeding to the ethyl-iodoacetamide, covalent linkage to cysteine protein sites is achieved efficiently as shown with a cyanobacterial phytochrome, extending the scarce application of SNARF in bio-labelling in the current literature. Application in fluorescence lifetime imaging is demonstrated both with the lifetime-based and ratiometric-yield method.



Citation Styles

Harvard Citation styleRichter, C., Schneider, C., Quick, M., Volz, P., Mahrwald, R., Hughes, J., et al. (2015) Dual-fluorescence pH probe for bio-labelling, Physical Chemistry Chemical Physics, 17(45), pp. 30590-30597. https://doi.org/10.1039/c5cp05454k

APA Citation styleRichter, C., Schneider, C., Quick, M., Volz, P., Mahrwald, R., Hughes, J., Dick, B., Alexiev, U., & Ernsting, N. (2015). Dual-fluorescence pH probe for bio-labelling. Physical Chemistry Chemical Physics. 17(45), 30590-30597. https://doi.org/10.1039/c5cp05454k


Last updated on 2025-10-06 at 10:33