Magnetic resonance is essential in revealing the structure and dynamics of biomolecules. However, measuring the magnetic resonance spectrum of single biomolecules has remained an elusive goal. We demonstrate the detection of the electron spin resonance signal from a single spin-labeled protein under ambient conditions. As a sensor, we use a single nitrogen vacancy center in bulk diamond in close proximity to the protein. We measure the orientation of the spin label at the protein and detect the impact of protein motion on the spin label dynamics. In addition, we coherently drive the spin at the protein, which is a prerequisite for studies involving polarization of nuclear spins of the protein or detailed structure analysis of the protein itself.

The measurement of the microwave field is crucial for many developments in microwave technology and related applications. However, measuring microwave fields with high sensitivity and spatial resolution under ambient conditions remains elusive. In this work, we propose and experimentally demonstrate a scheme to measure both the strength and orientation of the microwave magnetic field by utilizing the quantum coherent dynamics of nitrogen vacancy centres in diamond. An angular resolution of 5.7 mrad and a sensitivity of 1.0 μT Hz−1/2 are achieved at a microwave frequency of 2.6000 GHz, and the microwave magnetic field vectors generated by a copper wire are precisely reconstructed. The solid-state microwave magnetometry with high resolution and wide frequency range that can work under ambient conditions proposed here enables unique potential applications over other state-of-art microwave magnetometry.