Scanning tunneling microscopy (STM) can be used to image individual biological molecules, such as proteins, in vacuum or air. This requires sample dehydration and thus may not reflect the native state of the molecule. Extensive efforts have been made to image single proteins in solution using STM; however, the images have revealed only round or oval shapes with no sub-molecular details. Here, we present the sub-molecular features of streptavidin proteins under physiological conditions using a homebuilt low-leakage-current and highstability liquid phase STM. The N-lobe, C-lobe, and C-terminal tail of the epidermal growth factor receptor kinase domains were also resolved in solution. Our results demonstrate that the structure, morphology, and dynamics of a protein molecule can be examined under physiological conditions by the STM.

We report the first atomically resolved scanning tunneling microscope (STM) imaging in a water-cooled magnet (WM), for which extremely harsh vibrations and noise have been the major challenge. This custom WM-STM features an ultra-rigid and compact scan head in which the coarse approach is driven by our newly designed TunaDrive piezoelectric motor. A three-level spring hanging system is used for vibration isolation. Room-temperature raw-data images of graphite with quality atomic resolution were acquired in the presence of very strong magnetic fields, with a field strength up to 27 T, in a 32-mm-diameter bore WM with a maximum field strength of 27.5 T at a power rating of 10 MW, calibrated by nuclear magnetic resonance (NMR). This record field strength of 27 T exceeds the maximal field strength achieved by the conventional superconducting magnets. Besides, our WM-STM has paved the way to STM imaging using a 45 T, 32-mm-diameter bore hybrid magnet, which is the world's flagship magnet, producing the strongest steady magnetic field.