TY - JOUR
T1 - Dual Recognition DNA Triangular Prism Nanoprobe
T2 - Toward the Relationship between K+and pH in Lysosomes
AU - Li, Xiao Qiong
AU - Liu, Xiang Nan
AU - Jia, Yi Lei
AU - Luo, Xi Liang
AU - Chen, Hong Yuan
AU - Xu, Jing Juan
N1 - Publisher Copyright:
© 2021 American Chemical Society
PY - 2021/11/9
Y1 - 2021/11/9
N2 - Lysosomal acidification is essential for its degradative function, and the flux of H+correlated with that of K+in lysosomes. However, there is little research on their correlation due to the lack of probes that can simultaneously image these two ions. To deeply understand the role of K+in lysosomal acidification, here, we designed and fabricated a nanodevice using a K+-aptamer and two pH-triggered nanoswitches incorporated into a DNA triangular prism (DTP) as a dual signal response platform to simultaneously visualize K+and pH in lysosomes by a fluorescence method. This strategy could conveniently integrate two signal recognition modules into one probe, so as to achieve the goal of sensitive detection of two kinds of signals in the same time and space, which is suitable for the detection of various signals with the correlation of concentration. By co-imaging both K+and H+in lysosomes, we found that the efflux of K+was accompanied by a decrease of pH, which is of great value in understanding lysosomal acidification. Moreover, this strategy also has broad prospects as a versatile optical sensing platform for multiplexed analysis of other biomolecules in living cells.
AB - Lysosomal acidification is essential for its degradative function, and the flux of H+correlated with that of K+in lysosomes. However, there is little research on their correlation due to the lack of probes that can simultaneously image these two ions. To deeply understand the role of K+in lysosomal acidification, here, we designed and fabricated a nanodevice using a K+-aptamer and two pH-triggered nanoswitches incorporated into a DNA triangular prism (DTP) as a dual signal response platform to simultaneously visualize K+and pH in lysosomes by a fluorescence method. This strategy could conveniently integrate two signal recognition modules into one probe, so as to achieve the goal of sensitive detection of two kinds of signals in the same time and space, which is suitable for the detection of various signals with the correlation of concentration. By co-imaging both K+and H+in lysosomes, we found that the efflux of K+was accompanied by a decrease of pH, which is of great value in understanding lysosomal acidification. Moreover, this strategy also has broad prospects as a versatile optical sensing platform for multiplexed analysis of other biomolecules in living cells.
UR - http://www.scopus.com/inward/record.url?scp=85118720216&partnerID=8YFLogxK
U2 - 10.1021/acs.analchem.1c04056
DO - 10.1021/acs.analchem.1c04056
M3 - Article
AN - SCOPUS:85118720216
SN - 0003-2700
VL - 93
SP - 14892
EP - 14899
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 44
ER -