2006
DOI: 10.1002/adma.200601651
|View full text |Cite
|
Sign up to set email alerts
|

Protein Detecting Arrays Based on Cationic Polythiophene–DNA‐Aptamer Complexes

Abstract: By combining an appropriate DNA aptamer with a cationic polythiophene optical transducer, human thrombin can be specifically detected on microarrays in the attomole range in less than one hour without any tagging of the target. The system can be modified and utilized as a probe for the detection of various proteins or other biomolecules. This work opens new interesting possibilities for simple and rapid multiparametric analysis in genomics and proteomics.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
27
0

Year Published

2007
2007
2021
2021

Publication Types

Select...
5
4

Relationship

0
9

Authors

Journals

citations
Cited by 110 publications
(27 citation statements)
references
References 18 publications
0
27
0
Order By: Relevance
“…34,66 Compared with solid-state sensors based on the CP-dye FRET system, it showed merits of more simple, faster and low-cost since tedious operation (centrifugation, washing, drying, and ultrasonic operation) and long assay time were required for the solid-state detection. 66,75 In addition, our strategy also shows merits of fast, low-cost, label-free, and sensitive compared with fluorometric methods based on QDs-dye FRET system because the conjugation of biomolecules on the surface of QDs needs long time (several hours ) and labeled DNAs are much expensive than unlabeled ones. [67][68][69] Thus,…”
Section: ■ Results and Discussionmentioning
confidence: 98%
“…34,66 Compared with solid-state sensors based on the CP-dye FRET system, it showed merits of more simple, faster and low-cost since tedious operation (centrifugation, washing, drying, and ultrasonic operation) and long assay time were required for the solid-state detection. 66,75 In addition, our strategy also shows merits of fast, low-cost, label-free, and sensitive compared with fluorometric methods based on QDs-dye FRET system because the conjugation of biomolecules on the surface of QDs needs long time (several hours ) and labeled DNAs are much expensive than unlabeled ones. [67][68][69] Thus,…”
Section: ■ Results and Discussionmentioning
confidence: 98%
“…A conjugated polyelectrolyte (CPE)1, 2 a conjugated polymer containing a charged (anionic or cationic) group, has received considerable attention for its bio‐applications such as solution‐based DNA sensor,3–11 DNA microarray,12–14 protein sensor,15–24 bioimaging25–28 as well as optoelectronic applications such as organic semiconductors,29–31 light‐emitting devices,32, 33 and actuators 34. The ionic side group plays an important role to provide CPEs with water‐solubility that is central to many biological applications.…”
Section: Introductionmentioning
confidence: 99%
“…The advantages of CPs mean that they can be employed in protein detection with a label‐free manner. More importantly, highly charged CPs can be easily assembled on solid platforms to meet the demands of high‐throughput assay, which has been developed as a novel orientation for protein detection . However, relying on their electrostatic interactions with protein, it is difficult to obtain a response of fluorescent signal to the target protein binding events.…”
Section: Methodsmentioning
confidence: 99%