Add like
Add dislike
Add to saved papers

Light-Up Nonthiolated Aptasensor for Low-Mass, Soluble Amyloid-β 40 Oligomers at High Salt Concentrations.

Analytical Chemistry 2018 Februrary 7
Herein, a light-up nonthiolated aptasensor was developed for low-mass, soluble amyloid-β40 oligomers (LS-Aβ40-O ). Au nanoparticles (AuNP) were employed as colorimetric probes, and the nonthiolated aptamers (Apt) were adsorbed on AuNP surfaces, acting as binding elements for LS-Aβ40-O . The aggregation of AuNPs was induced when Apt-modified AuNPs (Apt@AuNPs) were under high-salt conditions. However, upon the addition of LS-Aβ40-O into the Apt@AuNP solution, the salt tolerance of the AuNPs was greatly enhanced. Further studies confirmed that the formed LS-Aβ40-O -Apt complex attached onto the AuNP surfaces via interactions between LS-Aβ40-O and Au, which led to electrostatic and steric stabilization of the AuNPs under high-salt conditions. On the basis of this outcome, a sensitive light-up nonthiolated aptasensor for LS-Aβ40-O was achieved with a detection limit of 10.0 nM and a linear range from 35.0 to 700 nM in a 175 mM NaCl solution. Cerebrospinal-fluid (CSF) samples from healthy persons and Alzheimer's disease (AD) patients were successfully distinguished by using this proposed method. The concentrations of LS-Aβ40-O in the CSF of AD patients were of nanomolar grade, but there was no detectable LS-Aβ40-O in those of the healthy persons. This work provides a new insight into the interaction between Apt@AuNPs and Aβ40-O and also develops a simple, rapid, highly selective and sensitive, and applicable method for LS-Aβ40-O detection in real CSF samples, which is significant for the diagnosis of AD.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app