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A Hybrid Orbitrap-Nanoelectromechanical Systems Approach for the Analysis of Individual, Intact Proteins in Real Time.
Neumann, Adam P; Sage, Eric; Boll, Dmitri; Reinhardt-Szyba, Maria; Fon, Warren; Masselon, Christophe; Hentz, Sébastien; Sader, John E; Makarov, Alexander; Roukes, Michael L.
Affiliation
  • Neumann AP; Kavli Nanoscience Institute and Department of Physics, California Institute of Technology, Pasadena, California, 91125, USA.
  • Sage E; Kavli Nanoscience Institute and Department of Physics, California Institute of Technology, Pasadena, California, 91125, USA.
  • Boll D; Thermo Fisher Scientific, 28199, Bremen, Germany.
  • Reinhardt-Szyba M; Thermo Fisher Scientific, 28199, Bremen, Germany.
  • Fon W; Kavli Nanoscience Institute and Department of Physics, California Institute of Technology, Pasadena, California, 91125, USA.
  • Masselon C; Univ. Grenoble Alpes, CEA, IRIG, Biologie à Grande Echelle, INSERM UA 13, F-38054, Grenoble, France.
  • Hentz S; Univ. Grenoble Alpes, CEA, Leti, F-38000, Grenoble, France.
  • Sader JE; Graduate Aerospace Laboratories and Department of Applied Physics, California Institute of Technology, Pasadena, California, 91125, USA.
  • Makarov A; Thermo Fisher Scientific, 28199, Bremen, Germany.
  • Roukes ML; Biomolecular Mass Spectrometry and Proteomics, Bijvoet Center for Biomolecular Research and Utrecht Institute for Pharmaceutical Sciences, University of Utrecht, Padualaan 8, 3584 CH, Utrecht, The Netherlands.
Angew Chem Int Ed Engl ; 63(33): e202317064, 2024 Aug 12.
Article in En | MEDLINE | ID: mdl-38769756
ABSTRACT
Nanoelectromechanical systems (NEMS)-based mass spectrometry (MS) is an emerging technique that enables determination of the mass of individual adsorbed particles by driving nanomechanical devices at resonance and monitoring the real-time changes in their resonance frequencies induced by each single molecule adsorption event. We incorporate NEMS into an Orbitrap mass spectrometer and report our progress towards leveraging the single-molecule capabilities of the NEMS to enhance the dynamic range of conventional MS instrumentation and to offer new capabilities for performing deep proteomic analysis of clinically relevant samples. We use the hybrid instrument to deliver E. coli GroEL molecules (801 kDa) to the NEMS devices in their native, intact state. Custom ion optics are used to focus the beam down to 40 µm diameter with a maximum flux of 25 molecules/second. The mass spectrum obtained with NEMS-MS shows good agreement with the known mass of GroEL.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chaperonin 60 / Nanotechnology / Escherichia coli Language: En Journal: Angew Chem Int Ed Engl Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chaperonin 60 / Nanotechnology / Escherichia coli Language: En Journal: Angew Chem Int Ed Engl Year: 2024 Document type: Article Affiliation country: Country of publication: