An electric field enhanced by a metallic nanoprobe has locally induced coherent anti-Stokes Raman scattering (CARS) of adenine molecules in a nanometric DNA network structure. Owing to the third-order nonlinearity, the excitation of the CARS polarization is extremely confined to the end of the tip apex, resulting in a spatial resolution far beyond the diffraction limit of light. Our tip-enhanced CARS microscope visualized the DNA network structure at a specific vibrational frequency (approximately 1337 cm(-1)) corresponding to the ring-breathing mode of diazole of adenine molecules.

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Kinesin-1, the founding member of the kinesin superfamily of proteins, is known to use only a subset of microtubules for transport in living cells. This biased use of microtubules is proposed as the guidance cue for polarized transport in neurons, but the underlying mechanisms are still poorly understood. Here, we report that kinesin-1 binding changes the microtubule lattice and promotes further kinesin-1 binding. This high-affinity state requires the binding of kinesin-1 in the nucleotide-free state. Microtubules return to the initial low-affinity state by washing out the binding kinesin-1 or by the binding of non-hydrolyzable ATP analogue AMPPNP to kinesin-1. X-ray fiber diffraction, fluorescence speckle microscopy, and second-harmonic generation microscopy, as well as cryo-EM, collectively demonstrated that the binding of nucleotide-free kinesin-1 to GDP microtubules changes the conformation of the GDP microtubule to a conformation resembling the GTP microtubule.

Tip-enhanced Raman scattering microscopy is a powerful technique for analysing nanomaterials at high spatial resolution far beyond the diffraction limit of light. However, imaging of intrinsic properties of materials such as individual molecules or local structures has not yet been achieved even with a tip-enhanced Raman scattering microscope. Here we demonstrate colour-coded tip-enhanced Raman scattering imaging of strain distribution along the length of a carbon nanotube. The strain is induced by dragging the nanotube with an atomic force microscope tip. A silver-coated nanotip is employed to enhance and detect Raman scattering from specific locations of the nanotube directly under the tip apex, representing deformation of its molecular alignment because of the existence of local strain. Our technique remarkably provides an insight into localized variations of structural properties in nanomaterials, which could prove useful for a variety of applications of carbon nanotubes and other nanomaterials as functional devices and materials.

We present a near-field Raman investigation in the subnanometric vicinity of a metallic nanotip, where the tip-sample distance is precisely controlled by our newly developed time-gated illumination technique. Using this scheme on an isolated carbon nanotube, we have profiled the spatial decay of evanescent light. We also investigated extremely short-ranged chemical and mechanical interactions between the metal on the tip apex and the molecules of an adenine sample, which are observable only within the subnanometric vicinity of the tip. The results show a near-field Raman investigation with an accuracy of better than a few angstroms. Further, this shows strong promise for superhigh resolution in optical microscopy based on this technique.