dc.contributor.author |
Barik, A. |
|
dc.contributor.author |
Sudhir, C. |
|
dc.contributor.author |
Wittenberg, N.J. |
|
dc.contributor.author |
Johnson, T.W. |
|
dc.contributor.author |
Oh, S-H. |
|
dc.date.accessioned |
2019-05-24T09:52:17Z |
|
dc.date.available |
2019-05-24T09:52:17Z |
|
dc.date.issued |
2016 |
|
dc.identifier.citation |
Analytical Chemistry. 88(3); 2016; 1704-1710. |
en_US |
dc.identifier.uri |
https://doi.org/10.1021/acs.analchem.5b03719 |
|
dc.identifier.uri |
http://irgu.unigoa.ac.in/drs/handle/unigoa/5670 |
|
dc.description.abstract |
Chemical analysis of membrane-bound containers such as secretory vesicles, organelles, and exosomes can provide insights into subcellular biology. These containers are loaded with a range of important biomolecules, which further underscores the need for sensitive and selective analysis methods. Here we present a metallic pyramid array for intravesicular analysis by combining site-selective dielectrophoresis (DEP) and Raman spectroscopy. Sharp pyramidal tips act as a gradient force generator to trap nanoparticles or vesicles from the solution, and the tips are illuminated by a monochromatic light source for concurrent spectroscopic detection of trapped analytes. The parameters suitable for DEP trapping were optimized by fluorescence microscopy, and the Raman spectroscopy setup was characterized by a nanoparticle based model system. Finally, vesicles loaded with 4-mercaptopyridine were concentrated at the tips and their Raman spectra were detected in real time. These pyramidal tips can perform large-area array-based trapping and spectroscopic analysis, opening up possibilities to detect molecules inside cells or cell-derived vesicles. |
en_US |
dc.publisher |
American Chemical Society |
en_US |
dc.subject |
Physics |
en_US |
dc.title |
Dielectrophoresis-assisted Raman spectroscopy of intravesicular analytes on metallic pyramids |
en_US |
dc.type |
Journal article |
en_US |
dc.identifier.impf |
y |
|