4.6 Article

Dual-fluorescence pH probe for bio-labelling

Journal

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 17, Issue 45, Pages 30590-30597

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5cp05454k

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Funding

  1. Deutsche Forschungsgemeinschaft (Collaborative Research Center 1078 Protonation Dynamics in Protein Function)
  2. Deutsche Forschungsgemeinschaft (Collaborative Research Center 1112 Nanocarriers: Architecture, Transport, and Topical Application of Drugs for Therapeutic Use'')

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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.

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