He Hua, Liu Lihua, Chen Xiaoliang, Wang Qian, Wang Xiaojuan, Nau Werner M, Huang Fang
State Key Laboratory of Heavy Oil Processing and College of Chemical Engineering China, University of Petroleum (East China), Qingdao 266580, China.
Department of Life Sciences and Chemistry, Jacobs University Bremen, Campus Ring 1, Bremen 28759, Germany.
Anal Chem. 2021 Mar 2;93(8):3968-3975. doi: 10.1021/acs.analchem.0c04885. Epub 2021 Feb 18.
Accurate counting of single molecules at nanoscale resolution is essential for the study of molecular interactions and distribution in subcellular fractions. By using small-sized carbon dots (CDs), we have now developed a quantitative single-molecule localization microscopy technique (qSMLM) based on spontaneous blinking to count single molecules with a localization precision of 10 nm, which can be accomplished on conventional microscopes without sophisticated laser control. We explore and adapt the blinking of CDs with diverse structures and demonstrate a counting accuracy of >97% at a molecular density of 500 per μm. When applied to G-protein coupled receptors on a cell membrane, we discriminated receptor oligomerization and clustering and revealed ligand-regulated receptor distribution patterns. This is the first example of adapting nanoparticle self-blinking for molecular counting, and this demonstrates the power of CDs as SMLM probes to reliably decipher sub-diffraction structures that mediate crucial biological functions.
在纳米尺度分辨率下准确计数单分子对于研究亚细胞组分中的分子相互作用和分布至关重要。通过使用小尺寸碳点(CDs),我们现已开发出一种基于自发闪烁的定量单分子定位显微镜技术(qSMLM),能够以10纳米的定位精度对单分子进行计数,这可以在无需复杂激光控制的传统显微镜上实现。我们探索并利用了具有不同结构的碳点的闪烁特性,在分子密度为每平方微米500个分子时,计数准确率超过97%。当应用于细胞膜上的G蛋白偶联受体时,我们区分了受体的寡聚化和聚集,并揭示了配体调节的受体分布模式。这是将纳米颗粒自闪烁用于分子计数的首个实例,证明了碳点作为单分子定位显微镜探针在可靠解析介导关键生物学功能的亚衍射结构方面的强大能力。