Development and Evaluation of a Reverse-Entry Ion Source Orbitrap Mass Spectrometer.

J Am Soc Mass Spectrom

Department of Chemistry, Texas A&M University, College Station, TX, 77843, USA.

Published: January 2019

AI Article Synopsis

  • - The text discusses the creation of a reverse-entry ion source (REIS) to enhance a high-resolution ion mobility mass spectrometer based on the orbitrap platform, marking an initial step toward developing a drift tube ion mobility-orbitrap MS.
  • - The REIS maintains the functionality of existing commercial ion sources, allowing for ongoing use of the instrument and enabling performance comparisons between the new and traditional sources.
  • - Testing with model proteins, ubiquitin and the AmtB protein complex, showed that the REIS provides similar mass resolution and consistent charge state distributions, indicating it effectively preserves the proteins' native structures in the gas phase.

Article Abstract

As a step towards development of a high-resolution ion mobility mass spectrometer using the orbitrap mass analyzer platform, we describe herein a novel reverse-entry ion source (REIS) coupled to the higher-energy C-trap dissociation (HCD) cell of an orbitrap mass spectrometer with extended mass range. Development of the REIS is a first step in the development of a drift tube ion mobility-orbitrap MS. The REIS approach retains the functionality of the commercial instrument ion source which permits the uninterrupted use of the instrument during development as well as performance comparisons between the two ion sources. Ubiquitin (8.5 kDa) and lipid binding to the ammonia transport channel (AmtB, 126 kDa) protein complex were used as model soluble and membrane proteins, respectively, to evaluate the performance of the REIS instrument. Mass resolution obtained with the REIS is comparable to that obtained using the commercial ion source. The charge state distributions for ubiquitin and AmtB obtained on the REIS are in agreement with previous studies which suggests that the REIS-orbitrap EMR retains native structure in the gas phase. Graphical Abstract ᅟ.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251776PMC
http://dx.doi.org/10.1007/s13361-018-1976-0DOI Listing

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