Zhang Zuo, Zhou Haisen, Xu Zhun, Wu Guangqi, Lu Hua, Wang Huan
Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering, Key Laboratory of Polymer Chemistry & Physics, Beijing 100871, People's Republic of China.
National Biomedical Imaging Center, Peking University, Beijing 100871, People's Republic of China.
JACS Au. 2024 Dec 16;5(1):261-270. doi: 10.1021/jacsau.4c00928. eCollection 2025 Jan 27.
Individual molecules dissolved in a dilute solution are usually considered not to correlate with each other as they undergo chemical reactions due to the mismatch of the diffusion and reaction time scales. Recent studies suggest otherwise, especially for reactions involving macromolecules. With selenopolypeptides as a model system, we used ensemble measurements and single-molecule direct imaging to investigate the correlation between physically constrained chemical reaction sites on a linear polymer chain and the coupling effects between conformation changes and reaction kinetics. We used graphene liquid cells to encapsulate and image the reaction of selenopolypeptides and observed helix-to-coil transitions as Se atoms are oxidized under liquid-phase electron microscopy. Three common pathways were identified among three kinds of selenopolypeptides that differ only in the side groups attached to the Se atoms, which were found to critically determine the observed cooperativity. A more hydrophobic side group appeared to slow the reaction rate, which allowed us to quantify the reaction kinetics in detail and observe the correlation between the reaction sites on a single chain.
溶解在稀溶液中的单个分子在发生化学反应时,由于扩散和反应时间尺度不匹配,通常被认为彼此之间不相关。然而,最近的研究表明并非如此,特别是对于涉及大分子的反应。以硒代多肽为模型系统,我们使用系综测量和单分子直接成像技术,研究了线性聚合物链上物理受限的化学反应位点之间的相关性,以及构象变化与反应动力学之间的耦合效应。我们使用石墨烯液体池来封装和成像硒代多肽的反应,并在液相电子显微镜下观察到随着硒原子被氧化,螺旋到线圈的转变。在仅在连接到硒原子的侧基上不同的三种硒代多肽中,确定了三种常见途径,发现这些途径对观察到的协同性起关键作用。一个更疏水的侧基似乎减缓了反应速率,这使我们能够详细量化反应动力学,并观察单链上反应位点之间的相关性。