Chan Arnold M, Ebrahimi Sasha B, Samanta Devleena, Leshchev Denis, Nijhawan Adam K, Hsu Darren J, Ho Madeline B, Ramani Namrata, Kosheleva Irina, Henning Robert, Mirkin Chad A, Kohlstedt Kevin L, Chen Lin X
Department of Chemistry, Northwestern University, Evanston, Illinois 60208, United States.
International Institute for Nanotechnology, Northwestern University, Evanston, Illinois 60208, United States.
J Am Chem Soc. 2024 Dec 11;146(49):33743-33752. doi: 10.1021/jacs.4c11768. Epub 2024 Nov 28.
The i-motif is a pH-responsive cytosine-rich oligonucleotide sequence that forms, under acidic conditions, a quadruplex structure. This tunable structural switching has made the i-motif a useful platform for designing pH-responsive nanomaterials. Despite the widespread application of i-motif DNA constructs as biomolecular switches, the mechanism of i-motif folding on the atomic scale has yet to be established. We investigate the early folding structural dynamics of i-motif oligonucleotides with laser-pulse-induced pH-jump time-resolved X-ray solution scattering. Following the pH-jump, we observe that the initial random coil ensemble converts into a contracted intermediate state within 113 ns followed by further folding on the 10 ms time scale. We reveal the representative structures of these transient species, hitherto unknown, with molecular dynamics simulations and ensemble fitting. These results pave the way for understanding metastable conformations of i-motif folding and for benchmarking emerging theoretical models for simulating noncanonical nucleic acid structures.
i-基序是一种富含胞嘧啶的pH响应性寡核苷酸序列,在酸性条件下形成四链体结构。这种可调节的结构转换使i-基序成为设计pH响应性纳米材料的有用平台。尽管i-基序DNA构建体作为生物分子开关得到了广泛应用,但i-基序在原子尺度上的折叠机制尚未确立。我们利用激光脉冲诱导的pH跃变时间分辨X射线溶液散射研究了i-基序寡核苷酸的早期折叠结构动力学。在pH跃变后,我们观察到初始的无规卷曲聚集体在113纳秒内转变为收缩的中间状态,随后在10毫秒的时间尺度上进一步折叠。我们通过分子动力学模拟和系综拟合揭示了这些迄今未知的瞬态物种的代表性结构。这些结果为理解i-基序折叠的亚稳态构象以及为模拟非经典核酸结构的新兴理论模型提供基准铺平了道路。