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| Main Authors: | , , , , , , , , , , , , , , , , |
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| Format: | Preprint |
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2025
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| Subjects: | |
| Online Access: | https://arxiv.org/abs/2512.10269 |
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| _version_ | 1866909956590010368 |
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| author | Li, Min Zhang, Qi Kong, Xi Zhao, Sheng Pan, Bin-Bin Sun, Ziting Yu, Pei Wang, Zhecheng Wang, Mengqi Ji, Wentao Kong, Fei Cheng, Guanglei Wu, Si Wang, Ya Chen, Sanyou Su, Xun-Cheng Shi, Fazhan |
| author_facet | Li, Min Zhang, Qi Kong, Xi Zhao, Sheng Pan, Bin-Bin Sun, Ziting Yu, Pei Wang, Zhecheng Wang, Mengqi Ji, Wentao Kong, Fei Cheng, Guanglei Wu, Si Wang, Ya Chen, Sanyou Su, Xun-Cheng Shi, Fazhan |
| contents | The investigation of biomolecular interactions at the single-molecule level has emerged as a pivotal research area in life science, particularly through optical, mechanical, and electrochemical approaches. Spins existing widely in biological systems, offer a unique degree of freedom for detecting such interactions. However, most previous studies have been largely confined to ensemble-level detection in the spin degree. Here, we developed a molecular interaction analysis method approaching single-molecule level based on relaxometry using the quantum sensor, nitrogen-vacancy (NV) center in diamond. Experiments utilized an optimized diamond surface functionalized with a polyethylenimine nanogel layer, achieving $\sim$10 nm average protein distance and mitigating interfacial steric hindrance. Then we measured the strong interaction between streptavidin and spin-labeled biotin complexes, as well as the weak interaction between bovine serum albumin and biotin complexes, at both the micrometer scale and nanoscale. For the micrometer-scale measurements using ensemble NV centers, we re-examined the often-neglected fast relaxation component and proposed a relaxation rate evaluation method, substantially enhancing the measurement sensitivity. Furthermore, we achieved nanoscale detection approaching single-molecule level using single NV centers. This methodology holds promise for applications in molecular screening, identification and kinetic studies at the single-molecule level, offering critical insights into molecular function and activity mechanisms. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2512_10269 |
| institution | arXiv |
| publishDate | 2025 |
| record_format | arxiv |
| spellingShingle | Quantum relaxometry for detecting biomolecular interactions with single NV centers Li, Min Zhang, Qi Kong, Xi Zhao, Sheng Pan, Bin-Bin Sun, Ziting Yu, Pei Wang, Zhecheng Wang, Mengqi Ji, Wentao Kong, Fei Cheng, Guanglei Wu, Si Wang, Ya Chen, Sanyou Su, Xun-Cheng Shi, Fazhan Quantum Physics Biological Physics The investigation of biomolecular interactions at the single-molecule level has emerged as a pivotal research area in life science, particularly through optical, mechanical, and electrochemical approaches. Spins existing widely in biological systems, offer a unique degree of freedom for detecting such interactions. However, most previous studies have been largely confined to ensemble-level detection in the spin degree. Here, we developed a molecular interaction analysis method approaching single-molecule level based on relaxometry using the quantum sensor, nitrogen-vacancy (NV) center in diamond. Experiments utilized an optimized diamond surface functionalized with a polyethylenimine nanogel layer, achieving $\sim$10 nm average protein distance and mitigating interfacial steric hindrance. Then we measured the strong interaction between streptavidin and spin-labeled biotin complexes, as well as the weak interaction between bovine serum albumin and biotin complexes, at both the micrometer scale and nanoscale. For the micrometer-scale measurements using ensemble NV centers, we re-examined the often-neglected fast relaxation component and proposed a relaxation rate evaluation method, substantially enhancing the measurement sensitivity. Furthermore, we achieved nanoscale detection approaching single-molecule level using single NV centers. This methodology holds promise for applications in molecular screening, identification and kinetic studies at the single-molecule level, offering critical insights into molecular function and activity mechanisms. |
| title | Quantum relaxometry for detecting biomolecular interactions with single NV centers |
| topic | Quantum Physics Biological Physics |
| url | https://arxiv.org/abs/2512.10269 |