Steady-state spectroscopy of new biological probes

Research output: Chapter in Book/Report/Conference proceedingConference contribution

2 Citations (Scopus)

Abstract

The steady state absorption and fluorescence spectroscopy of 2-(2′-hydroxyphenyl)benzoxazole (HBO) and (2,2′-bipyridine)-3, 3′-diol (BP(OH)2) were studied here free in solution and in human serum albumin (HSA) in order to test their applicability as new biological probes. HBO and BP(OH)2 are known to undergo intramolecular proton transfers in the excited state. Their absorption and fluorescence spectra are sensitive to environmental change from hydrophilic to hydrophobic, thus allowing the opportunity to use them as environment-sensitive probes. The effect of water on the steady state spectra of the two molecules also shows unique features which may position them as water sensors in biological systems. For HBO in buffer, fluorescence is only due to the syn-keto tautomer, whereas in HSA the fluorescence is due to four species in equilibrium in the excited state (the syn-keto tautomer, the anti-enol tautomer, the solvated syn-enol tautomer, and the anion species of HBO). Analysis of the fluorescence spectra of HBO in HSA indicates that HBO is exposed to less water in the HBO:HSA complex. For the BP(OH)2 molecule, unique absorption due to water was observed in the spectral region of 400-450 nm. This absorption decreases in the presence of HSA due to less accessibility to water as a result of binding to HSA. Fluorescence of BP(OH)2 is due solely to the di-keto tautomer after double proton transfer in the excited state. The fluorescence peak of BP(OH)2 shows a red-shift upon HSA recognition which is attributed to the hydrophobic environment inside the binding site of HSA. We discuss also the effect of probe-inclusion inside well-defined hydrophobic cavities of cyclodextrins.

Original languageEnglish
Title of host publicationProgress in Biomedical Optics and Imaging - Proceedings of SPIE
Volume6449
DOIs
Publication statusPublished - 2007
EventGenetically Engineered and Optical Probes for Biomedical Applications IV - San Jose, CA, United States
Duration: Jan 23 2007Jan 24 2007

Other

OtherGenetically Engineered and Optical Probes for Biomedical Applications IV
CountryUnited States
CitySan Jose, CA
Period1/23/071/24/07

Fingerprint

Fluorescence
Spectroscopy
Excited states
Proton transfer
Water
Molecules
Cyclodextrins
Fluorescence spectroscopy
Biological systems
Binding sites
Absorption spectroscopy
Negative ions
Sensors

Keywords

  • (2,2′-Bipyridine)-3,3′- diol
  • 2-(2′-Hydroxyphenyl)benzoxazole
  • Cyclodextrins
  • Fluorescent probes
  • Human serum albumin
  • Protein-ligand recognition
  • Tautomerization

ASJC Scopus subject areas

  • Engineering(all)

Cite this

Abou-Zied, O. K. (2007). Steady-state spectroscopy of new biological probes. In Progress in Biomedical Optics and Imaging - Proceedings of SPIE (Vol. 6449). [64490L] https://doi.org/10.1117/12.703269

Steady-state spectroscopy of new biological probes. / Abou-Zied, Osama K.

Progress in Biomedical Optics and Imaging - Proceedings of SPIE. Vol. 6449 2007. 64490L.

Research output: Chapter in Book/Report/Conference proceedingConference contribution

Abou-Zied, OK 2007, Steady-state spectroscopy of new biological probes. in Progress in Biomedical Optics and Imaging - Proceedings of SPIE. vol. 6449, 64490L, Genetically Engineered and Optical Probes for Biomedical Applications IV, San Jose, CA, United States, 1/23/07. https://doi.org/10.1117/12.703269
Abou-Zied OK. Steady-state spectroscopy of new biological probes. In Progress in Biomedical Optics and Imaging - Proceedings of SPIE. Vol. 6449. 2007. 64490L https://doi.org/10.1117/12.703269
Abou-Zied, Osama K. / Steady-state spectroscopy of new biological probes. Progress in Biomedical Optics and Imaging - Proceedings of SPIE. Vol. 6449 2007.
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