Department of Applied Physics, Osaka University, 2-1 Yamadaoka, Suita Osaka 565-0871, Japan.
Department of Functional Materials, Saitama University, 225 Shimo-Okubo, Sakura-ku, Saitama 338-8570, Japan.
Colloids Surf B Biointerfaces. 2018 Jul 1;167:267-274. doi: 10.1016/j.colsurfb.2018.04.015. Epub 2018 Apr 13.
Conjugates of semiconductor quantum dots (QDs) and antibodies have emerged as a promising bioprobes due to their great combination of QD's efficient fluorescence and the high specificity of antigen-antibody reactions. For further developments in this field, it is essential to understand the molecular conformation of the QD-antibody conjugates at the single-molecule scale. Here, we report on the direct imaging of QD-antibody conjugates at the single-molecule scale by using high-speed atomic force microscopy (HS-AFM). Owing to the high spatiotemporal resolution of HS-AFM, we observed the dynamic splitting of individual antibodies during the conjugation process. QD-antibody conjugates were also clearly visualized at the single-molecule scale details. Several important features were even discovered through dynamic observation of the QD-antibody conjugates. We observed an intermediate state of conjugation, where the antibodies attached and detached to QDs repeatedly. We also revealed that the attached antibodies were not steady but drastically fluctuated in their recognition areas due to the Brownian motion. We also demonstrated that HS-AFM observation is useful for the quantitative analysis of fabricated conjugates.
半导体量子点 (QD) 和抗体的缀合物由于 QD 的高效荧光和抗原-抗体反应的高特异性的完美结合,已经成为一种很有前途的生物探针。为了在这个领域取得进一步的发展,了解 QD-抗体缀合物在单分子尺度上的分子构象是至关重要的。在这里,我们通过使用高速原子力显微镜 (HS-AFM) 报告了在单分子尺度上直接对 QD-抗体缀合物的成像。由于 HS-AFM 的高时空分辨率,我们观察到在缀合过程中单个抗体的动态分裂。QD-抗体缀合物也在单分子尺度细节上清晰可见。通过对 QD-抗体缀合物的动态观察,甚至发现了几个重要的特征。我们观察到了一个连接的中间状态,其中抗体反复连接和脱离 QD。我们还揭示了由于布朗运动,连接的抗体并不稳定,而是在它们的识别区域剧烈波动。我们还证明了 HS-AFM 观察对于制造的缀合物的定量分析是有用的。