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Lysine-functionalized silver nanoparticles for visual detection and separation of histidine and histidine-tagged proteins

Title
Lysine-functionalized silver nanoparticles for visual detection and separation of histidine and histidine-tagged proteins
Authors
Bae D.R.Han W.S.Lim J.M.Kang S.Lee J.Y.Kang D.Jung J.H.
Ewha Authors
강동민
SCOPUS Author ID
강동민scopus
Issue Date
2010
Journal Title
Langmuir
ISSN
0743-7463JCR Link
Citation
vol. 26, no. 3, pp. 2181 - 2185
Indexed
SCI; SCIE; SCOPUS WOS scopus
Abstract
A new chromogenic chemosensor based on lysine-functionalized silver nanoparticles 1 was prepared, and characterized by transmission electron microscopy (TEM), Fourier transform. Raman, and ultraviolet-visible (UV-vis) spectroscopy. The color changes of nanoparticles 1 in the absence and the presence of metal ion were observed, upon addition of various amino acids and proteins in aqueous solution. Among the various amino acids, the sensor 1 in the absence of metal ion shows a novel colorimetric sensor with capability to probe histidine and histidine-tagged proteins. On the other hand, the color changes of 1 in the presence of metal ions such as KCl or NiCl2 did not occur with any amino acids. Therefore, the sensor 1 in the absence of metal ion responds selectively to histidine, a response which can be attributed to its aggregation induced by histidine with high numbers of electrostatic interactions. This highly selective sensor 1 allows a rapid, quantitative assay of histidine to concentrations as low as 5.0 μM, providing a new tool for the direct measurement of histidine and histidine-tagged proteins in vitro system. Furthermore, we examined the effect of pH on absorbance (A520) of 1 in the presence of histidine (pH 4-12). The absorbance under basic conditions was higher than that under acidic or neutral conditions, in accord with the stronger aggregation of 1 with histidine by electrostatic interaction between the carboxylate anion of 1 and ammonium protons of histidine under basic conditions. © 2009 American Chemical Society.
DOI
10.1021/la9026865
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자연과학대학 > 생명과학전공 > Journal papers
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