Towards single-molecule nanomechanical mass spectrometry

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Abstract

Mass spectrometry provides rapid and quantitative identification of protein species with relatively low sample consumption. The trend towards biological analysis at increasingly smaller scales, ultimately down to the volume of an individual cell, continues, and mass spectrometry with a sensitivity of a few to single molecules will be necessary. Nanoelectromechanical systems provide unparalleled mass sensitivity, which is now sufficient for the detection of individual molecular species in real time. Here, we report the first demonstration of mass spectrometry based on single biological molecule detection with a nanoelectromechanical system. In our nanoelectromechanical–mass spectrometry system, nanoparticles and protein species are introduced by electrospray injection from the fluid phase in ambient conditions into vacuum, and are subsequently delivered to the nanoelectromechanical system detector by hexapole ion optics. Precipitous frequency shifts, proportional to the mass, are recorded in real time as analytes adsorb, one by one, onto a phase-locked, ultrahigh-frequency nanoelectromechanical resonator. These first nanoelectromechanical system–mass spectrometry spectra, obtained with modest mass sensitivity from only several hundred mass adsorption events, presage the future capabilities of this approach. We also outline the substantial improvements that are feasible in the near term, some of which are unique to nanoelectromechanical system based-mass spectrometry.

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Figure 1: First-generation NEMS–MS system.
Figure 2: Real-time records of single-molecule adsorption events on a NEMS mass sensor.
Figure 3: NEMS mass spectrometry of a gold nanoparticle dispersion.
Figure 4: NEMS–MS of proteins.

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Acknowledgements

We acknowledge support from the NIH under grant R21-GM072898 and, indirectly, from DARPA/MTO under DOI/NBCH1050001 (MGA program) and SPAWAR/ N66001-02-1-8914 (CSAC program). The latter has enabled development of critical NEMS technology for this work. We thank S. Stryker for expert technical assistance in constructing the NEMS-MS system, C. A. Zorman and M. Mehregany for custom SiC epilayers used in our NEMS fabrication, V. Semenchenko, D. A. Van Valen and R. Philips for help with gel electrophoresis, and I. Bargatin, J. L. Beauchamp, W. Lee, E. B. Myers and M. Shahgoli for helpful discussions.

Author information

A.K.N. and M.S.H. fabricated devices, performed experiments, analysed results and carried out some simulations. W.K.H. designed and assembled the system and performed the initial experiments. X.L.F. made the devices and did the initial phase-locked loop measurements. M.L.R. conceived the project and provided overall guidance throughout. All authors discussed the results and were involved in the analyses and manuscript preparation.

Correspondence to X. L. Feng or M. L. Roukes.

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Naik, A., Hanay, M., Hiebert, W. et al. Towards single-molecule nanomechanical mass spectrometry. Nature Nanotech 4, 445–450 (2009) doi:10.1038/nnano.2009.152

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