| Literature DB >> 25935260 |
Ileana M Pazos1, Ismail A Ahmed2, Mariana I León Berríos3, Feng Gai4.
Abstract
We expand the spectroscopic utility of a well-known infrared and fluorescence probe, p-cyanophenylalanine, by showing that it can also serve as a pH sensor. This new application is based on the notion that the fluorescence quantum yield of this unnatural amino acid, when placed at or near the N-terminal end of a polypeptide, depends on the protonation status of the N-terminal amino group of the peptide. Using this pH sensor, we are able to determine the N-terminal pKa values of nine tripeptides and also the membrane penetration kinetics of a cell-penetrating peptide. Taken together, these examples demonstrate the applicability of using this unnatural amino acid fluorophore to study pH-dependent biological processes or events that accompany a pH change.Entities:
Keywords: Cell-penetrating peptide; Fluorescence spectroscopy; N-terminal pK(a) of peptide; p-Cyanophenylalanine; pH sensor
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Year: 2015 PMID: 25935260 PMCID: PMC4461448 DOI: 10.1016/j.ab.2015.04.026
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365