Massively Parallel Selection of NanoCluster Beacons

© 2022 Wiley-VCH GmbH.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 34(2022), 41 vom: 01. Okt., Seite e2204957
1. Verfasser: Kuo, Yu-An (VerfasserIn)
Weitere Verfasser: Jung, Cheulhee, Chen, Yu-An, Kuo, Hung-Che, Zhao, Oliver S, Nguyen, Trung D, Rybarski, James R, Hong, Soonwoo, Chen, Yuan-I, Wylie, Dennis C, Hawkins, John A, Walker, Jada N, Shields, Samuel W J, Brodbelt, Jennifer S, Petty, Jeffrey T, Finkelstein, Ilya J, Yeh, Hsin-Chih
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2022
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article NanoCluster Beacons fluorescent nanomaterials high-throughput screening next-generation sequencing silver nanoclusters Nucleotides Silver 3M4G523W1G DNA 9007-49-2
Beschreibung
Zusammenfassung:© 2022 Wiley-VCH GmbH.
NanoCluster Beacons (NCBs) are multicolor silver nanocluster probes whose fluorescence can be activated or tuned by a proximal DNA strand called the activator. While a single-nucleotide difference in a pair of activators can lead to drastically different activation outcomes, termed polar opposite twins (POTs), it is difficult to discover new POT-NCBs using the conventional low-throughput characterization approaches. Here, a high-throughput selection method is reported that takes advantage of repurposed next-generation-sequencing chips to screen the activation fluorescence of ≈40 000 activator sequences. It is found that the nucleobases at positions 7-12 of the 18-nucleotide-long activator are critical to creating bright NCBs and positions 4-6 and 2-4 are hotspots to generate yellow-orange and red POTs, respectively. Based on these findings, a "zipper-bag" model is proposed that can explain how these hotspots facilitate the formation of distinct silver cluster chromophores and alter their chemical yields. Combining high-throughput screening with machine-learning algorithms, a pipeline is established to design bright and multicolor NCBs in silico
Beschreibung:Date Completed 17.10.2022
Date Revised 06.09.2024
published: Print-Electronic
Citation Status MEDLINE
ISSN:1521-4095
DOI:10.1002/adma.202204957