Issue 45, 2015

Dual-fluorescence pH probe for bio-labelling

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 pKa 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.

Graphical abstract: Dual-fluorescence pH probe for bio-labelling

Supplementary files

Article information

Article type
Paper
Submitted
12 Sep 2015
Accepted
16 Oct 2015
First published
19 Oct 2015
This article is Open Access
Creative Commons BY license

Phys. Chem. Chem. Phys., 2015,17, 30590-30597

Author version available

Dual-fluorescence pH probe for bio-labelling

C. Richter, C. Schneider, M. T. Quick, P. Volz, R. Mahrwald, J. Hughes, B. Dick, U. Alexiev and N. P. Ernsting, Phys. Chem. Chem. Phys., 2015, 17, 30590 DOI: 10.1039/C5CP05454K

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