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Single-protein nanomechanical mass spectrometry in real time

Nanoelectromechanical systems (NEMS) resonators can detect mass with exceptional sensitivity. Previously, mass spectra from several hundred adsorption events were assembled in NEMS-based mass spectrometry using statistical analysis. Here, we report the first realization of single-molecule NEMS-based...

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Detalles Bibliográficos
Autores principales: Hanay, M.S., Kelber, S., Naik, A.K., Chi, D., Hentz, S., Bullard, E.C., Colinet, E., Duraffourg, L., Roukes, M.L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3435450/
https://www.ncbi.nlm.nih.gov/pubmed/22922541
http://dx.doi.org/10.1038/nnano.2012.119
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author Hanay, M.S.
Kelber, S.
Naik, A.K.
Chi, D.
Hentz, S.
Bullard, E.C.
Colinet, E.
Duraffourg, L.
Roukes, M.L.
author_facet Hanay, M.S.
Kelber, S.
Naik, A.K.
Chi, D.
Hentz, S.
Bullard, E.C.
Colinet, E.
Duraffourg, L.
Roukes, M.L.
author_sort Hanay, M.S.
collection PubMed
description Nanoelectromechanical systems (NEMS) resonators can detect mass with exceptional sensitivity. Previously, mass spectra from several hundred adsorption events were assembled in NEMS-based mass spectrometry using statistical analysis. Here, we report the first realization of single-molecule NEMS-based mass spectrometry in real time. As each molecule in the sample adsorbs upon the NEMS resonator, its mass and the position-of-adsorption are determined by continuously tracking two driven vibrational modes of the device. We demonstrate the potential of multimode NEMS-based mass spectrometry by analyzing IgM antibody complexes in real-time. NEMS-MS is a unique and promising new form of mass spectrometry: it can resolve neutral species, provides resolving power that increases markedly for very large masses, and allows acquisition of spectra, molecule-by-molecule, in real-time.
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spelling pubmed-34354502013-03-01 Single-protein nanomechanical mass spectrometry in real time Hanay, M.S. Kelber, S. Naik, A.K. Chi, D. Hentz, S. Bullard, E.C. Colinet, E. Duraffourg, L. Roukes, M.L. Nat Nanotechnol Article Nanoelectromechanical systems (NEMS) resonators can detect mass with exceptional sensitivity. Previously, mass spectra from several hundred adsorption events were assembled in NEMS-based mass spectrometry using statistical analysis. Here, we report the first realization of single-molecule NEMS-based mass spectrometry in real time. As each molecule in the sample adsorbs upon the NEMS resonator, its mass and the position-of-adsorption are determined by continuously tracking two driven vibrational modes of the device. We demonstrate the potential of multimode NEMS-based mass spectrometry by analyzing IgM antibody complexes in real-time. NEMS-MS is a unique and promising new form of mass spectrometry: it can resolve neutral species, provides resolving power that increases markedly for very large masses, and allows acquisition of spectra, molecule-by-molecule, in real-time. 2012-08-26 2012-09 /pmc/articles/PMC3435450/ /pubmed/22922541 http://dx.doi.org/10.1038/nnano.2012.119 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Hanay, M.S.
Kelber, S.
Naik, A.K.
Chi, D.
Hentz, S.
Bullard, E.C.
Colinet, E.
Duraffourg, L.
Roukes, M.L.
Single-protein nanomechanical mass spectrometry in real time
title Single-protein nanomechanical mass spectrometry in real time
title_full Single-protein nanomechanical mass spectrometry in real time
title_fullStr Single-protein nanomechanical mass spectrometry in real time
title_full_unstemmed Single-protein nanomechanical mass spectrometry in real time
title_short Single-protein nanomechanical mass spectrometry in real time
title_sort single-protein nanomechanical mass spectrometry in real time
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3435450/
https://www.ncbi.nlm.nih.gov/pubmed/22922541
http://dx.doi.org/10.1038/nnano.2012.119
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