Department of Chemistry and Biochemistry, Kent State University, Kent, Ohio 44242, United States.
Advanced Materials and Liquid Crystals Institute, Kent State University, Kent, Ohio 44242, United States.
J Am Chem Soc. 2024 May 15;146(19):13046-13054. doi: 10.1021/jacs.3c14350. Epub 2024 May 6.
Common in biomacromolecules, kinetically trapped misfolded intermediates are often detrimental to the structures, properties, or functions of proteins or nucleic acids. Nature employs chaperone proteins but not nucleic acids to escort intermediates to correct conformations. Herein, we constructed a Jablonski-like diagram of a mechanochemical cycle in which individual DNA hairpins were mechanically unfolded to high-energy states, misfolded into kinetically trapped states, and catalytically relaxed back to ground-state hairpins by a DNA chaperone. The capacity of catalytic relaxation was demonstrated in a 1D DNA hairpin array mimicking nanoassembled materials. At ≥1 μM, the diffusive (or self-walking) DNA chaperone converted the entire array of misfolded intermediates to correct conformation in less than 15 s, which is essential to rapidly prepare homogeneous nanoassemblies. Such an efficient self-walking amplification increases the signal-to-noise ratio, facilitating catalytic relaxation to recognize a 1 fM DNA chaperone in 10 min, a detection limit comparable to the best biosensing strategies.
在生物大分子中,动力学捕获的错误折叠中间体通常对蛋白质或核酸的结构、性质或功能有害。自然界利用伴侣蛋白而不是核酸来护送中间体形成正确的构象。在此,我们构建了一个机械化学循环的 Jablonski 样图,其中单个 DNA 发夹被机械展开到高能状态,错误折叠成动力学捕获状态,并通过 DNA 伴侣蛋白催化松弛回到发夹的基态。在模拟纳米组装材料的 1D DNA 发夹阵列中证明了催化松弛的能力。在≥1μM 时,扩散(或自行走)的 DNA 伴侣蛋白可在不到 15 秒内将整个错误折叠中间体阵列转化为正确构象,这对于快速制备均匀的纳米组装体至关重要。这种高效的自行走扩增提高了信号与噪声的比率,有助于在 10 分钟内识别出 1 fM 的 DNA 伴侣蛋白,检测限可与最佳的生物传感策略相媲美。