Abstract
We demonstrate for the first time the utility of nucleic acid aptamers for electrochemical detection of proteins. Highly specific and sensitive label-free detection of the target protein is achieved by combining aptamer-coated magnetic beads and chronopotentiometric stripping measurements of the captured protein (in connection to the intrinsic electroactivity of the protein). Lysozyme has thus been detected selectively in a mixture containing a large excess of six proteins and amino acids (both electroactive and non-electroactive), with a detection limit of 350 fmol (7 nM). While aptamer-based electronic sensors are in their infancy, such devices offer attractive opportunities for electrochemical detection of proteins and for developing proteomic chips.
| Original language | English |
|---|---|
| Pages (from-to) | 537-540 |
| Number of pages | 4 |
| Journal | Electrochemistry Communications |
| Volume | 7 |
| Issue number | 5 |
| DOIs | |
| State | Published - May 2005 |
| Externally published | Yes |
Bibliographical note
Funding Information:This research was supported by grants from the National Science Foundation (Grant number CHE 0209707) and the NIH (Award No. R01A 1056047-01). M.C.R. acknowledges a fellowship from Fundacion Antorchas (Argentina).
Keywords
- Aptamers
- Bioelectronics
- Proteins
- Stripping potentiometry
ASJC Scopus subject areas
- Electrochemistry