| 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 |