Guanine-rich sequences exhibit a high degree of polymorphism and can form single-stranded, Watson-Crick duplex, and four-stranded G-quadruplex structures. These sequences have found a wide range of uses in synthetic biology applications, arising in part from their structural plasticity. High-throughput, low-cost tools for monitoring the folding and unfolding transitions of G-rich sequences would provide an enabling technology for accelerating the prototyping of synthetic biological systems and for accelerating design-build-test cycles. Here, we show that unfolding transitions of a range of G-quadruplex-forming DNA sequences can be monitored in a FRET-like format using DNA sequences that possess only a single dye label, with no quencher. These quencher-free assays can be performed at low cost, with both cost and lead times ca. 1 order of magnitude lower than FRET-labeled strands. Thus, quencher-free secondary structure monitoring promises to be a valuable tool for the testing and development of synthetic biology systems employing G-quadruplexes.
Quencher-Free Fluorescence Monitoring of G-Quadruplex Folding.
无淬灭剂荧光监测G-四链体折叠
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作者:Parada Zachary, Hoog Tanner G, Adamala Katarzyna P, Engelhart Aaron E
| 期刊: | ACS Omega | 影响因子: | 4.300 |
| 时间: | 2025 | 起止号: | 2025 Jan 15; 10(3):3176-3181 |
| doi: | 10.1021/acsomega.4c10720 | ||
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