Parada Zachary, Hoog Tanner G, Adamala Katarzyna P, Engelhart Aaron E
Department of Biochemistry, Molecular Biology and Biophysics, University of Minnesota, 321 Church Street SE, Minneapolis, Minnesota 55455, United States.
Department of Genetics, Cell Biology, and Development, University of Minnesota, 6-160 Jackson Hall, 321 Church Street SE, Minneapolis, Minnesota 55455, United States.
ACS Omega. 2025 Jan 15;10(3):3176-3181. doi: 10.1021/acsomega.4c10720. eCollection 2025 Jan 28.
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.
富含鸟嘌呤的序列表现出高度的多态性,能够形成单链、沃森-克里克双链以及四链G-四链体结构。这些序列在合成生物学应用中有着广泛的用途,部分原因在于它们的结构可塑性。用于监测富含G序列折叠和解折叠转变的高通量、低成本工具,将为加速合成生物系统的原型设计以及加速设计-构建-测试循环提供一项赋能技术。在此,我们表明,一系列形成G-四链体的DNA序列的解折叠转变,可以使用仅带有单个染料标签而无淬灭剂的DNA序列,以类似荧光共振能量转移(FRET)的形式进行监测。这些无淬灭剂的检测可以低成本进行,成本和周转时间均比FRET标记链低约1个数量级。因此,无淬灭剂的二级结构监测有望成为用于测试和开发采用G-四链体的合成生物学系统的一项有价值的工具。