TY - JOUR
T1 - Graphene Oxide-Assisted Nucleic Acids Assays Using Conjugated Polyelectrolytes-Based Fluorescent Signal Transduction
AU - Li, Fan
AU - Chao, Jie
AU - Li, Zhenhua
AU - Xing, Shu
AU - Su, Shao
AU - Li, Xiaoxia
AU - Song, Shiping
AU - Zuo, Xiaolei
AU - Fan, Chunhai
AU - Liu, Bin
AU - Huang, Wei
AU - Wang, Lianhui
AU - Wang, Lihua
N1 - Publisher Copyright:
© 2015 American Chemical Society.
PY - 2015/4/7
Y1 - 2015/4/7
N2 - In this work, we investigated the interactions between graphene oxide (GO) and conjugated polyelectrolytes (CPEs) with different backbone and side chain structures. By studying the mechanism of fluorescence quenching of CPEs by GO, we find that the charge and the molecular structure of CPEs play important roles for GO-CPEs interactions. Among them, electrostatic interaction, π-π interaction, and cation-π bonding are dominant driving forces. By using a cationic P2, we have developed a sensitive homogeneous sensor for DNA and RNA detection with a detection limit of 50 pM DNA and RNA, which increased the sensitivity by 40-fold as compared to GO-free CPE-based sensors. This GO-assisted CPE sensing strategy is also generic and shows a high potential for biosensor designs based on aptamers, proteins, peptides, and other biological probes. (Figure Presented).
AB - In this work, we investigated the interactions between graphene oxide (GO) and conjugated polyelectrolytes (CPEs) with different backbone and side chain structures. By studying the mechanism of fluorescence quenching of CPEs by GO, we find that the charge and the molecular structure of CPEs play important roles for GO-CPEs interactions. Among them, electrostatic interaction, π-π interaction, and cation-π bonding are dominant driving forces. By using a cationic P2, we have developed a sensitive homogeneous sensor for DNA and RNA detection with a detection limit of 50 pM DNA and RNA, which increased the sensitivity by 40-fold as compared to GO-free CPE-based sensors. This GO-assisted CPE sensing strategy is also generic and shows a high potential for biosensor designs based on aptamers, proteins, peptides, and other biological probes. (Figure Presented).
UR - http://www.scopus.com/inward/record.url?scp=84926620983&partnerID=8YFLogxK
U2 - 10.1021/ac504658a
DO - 10.1021/ac504658a
M3 - 文章
C2 - 25738486
AN - SCOPUS:84926620983
SN - 0003-2700
VL - 87
SP - 3877
EP - 3883
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 7
ER -