Single-nucleobase resolution of a surface energy transfer nanoruler for in situ measurement of aptamer binding at the receptor subunit level in living cells

In situ identification of aptamer-binding targets on living cell membrane surfaces is of considerable interest, but a major challenge, specifically, when advancing recognition to the level of membrane receptor subunits. Here we propose a novel nanometal surface energy transfer (NSET) based nanoruler with a single-nucleobase resolution (SN-nanoruler), in which FAM-labeled aptamers and single-sized gold nanoparticle (GNP) antibody conjugates act as a donor and an acceptor. A single nucleobase resolution of the SN-nanoruler was experimentally illustrated by molecular size, orientation, quenching nature, and other dye-GNP pairs. The SN-nanoruler provides high reproducibility and precision for measuring molecule distance on living cell membranes at the nanometer level owing to only the use of single-sized antibody-capped GNPs. In situ identification of the aptamer binding site was advanced to the protein subunit level on the living cell membrane for the utilization of this SN-nanoruler. The results suggest that the proposed strategy is a solid step towards the wider application of optical-based rulers to observe the molecular structural configuration and dynamic transitions on the membrane surface of living cells.

Automated summary

In this study, a novel nanometal surface energy transfer (NSET) nanoruler with a single-nucleobase resolution was proposed for in situ identification of aptamer-binding targets on living cell membrane surfaces. The nanoruler consisted of FAM-labeled aptamers and single-sized gold nanoparticle (GNP) antibody conjugates as a donor and an acceptor, respectively. Experimental evidence demonstrated the single nucleobase resolution of the nanoruler by molecular size, orientation, quenching nature, and other dye-GNP pairs. The nanoruler showed high reproducibility and precision for measuring molecule distance on living cell membranes at the nanometer level due to the use of only single-sized antibody-capped GNPs. The proposed strategy represents a solid step towards the wider application of optical-based rulers for observing molecular structural configuration and dynamic transitions on the membrane surface of living cells.