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Sulfur Pentafluoride is a Preferred Reagent Cation for Negative Electron Transfer Dissociation.


ABSTRACT: Negative mode proteome analysis offers access to unique portions of the proteome and several acidic post-translational modifications; however, traditional collision-based fragmentation methods fail to reliably provide sequence information for peptide anions. Negative electron transfer dissociation (NETD), on the other hand, can sequence precursor anions in a high-throughput manner. Similar to other ion-ion methods, NETD is most efficient with peptides of higher charge state because of the increased electrostatic interaction between reacting molecules. Here we demonstrate that NETD performance for lower charge state precursors can be improved by altering the reagent cation. Specifically, the recombination energy of the NETD reaction-largely dictated by the ionization energy (IE) of the reagent cation-can affect the extent of fragmentation. We compare the NETD reagent cations of C16H10?+ (IE?=?7.9 eV) and SF5?+ (IE?=?9.6 eV) on a set of standard peptides, concluding that SF5?+ yields greater sequence ion generation. Subsequent proteome-scale nLC-MS/MS experiments comparing C16H10?+ and SF5?+ further supported this outcome: analyses using SF5?+ yielded 4637 peptide spectral matches (PSMs) and 2900 unique peptides, whereas C16H10?+ produced 3563 PSMs and 2231 peptides. The substantive gain in identification power with SF5?+ was largely driven by improved identification of doubly deprotonated precursors, indicating that increased NETD recombination energy can increase product ion yield for low charge density precursors. This work demonstrates that SF5?+ is a viable, if not favorable, reagent cation for NETD, and provides improved fragmentation over the commonly used fluoranthene reagent. Graphical Abstract ?.

SUBMITTER: Rush MJP 

PROVIDER: S-EPMC5483201 | biostudies-literature | 2017 Jul

REPOSITORIES: biostudies-literature

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Sulfur Pentafluoride is a Preferred Reagent Cation for Negative Electron Transfer Dissociation.

Rush Matthew J P MJP   Riley Nicholas M NM   Westphall Michael S MS   Syka John E P JEP   Coon Joshua J JJ  

Journal of the American Society for Mass Spectrometry 20170327 7


Negative mode proteome analysis offers access to unique portions of the proteome and several acidic post-translational modifications; however, traditional collision-based fragmentation methods fail to reliably provide sequence information for peptide anions. Negative electron transfer dissociation (NETD), on the other hand, can sequence precursor anions in a high-throughput manner. Similar to other ion-ion methods, NETD is most efficient with peptides of higher charge state because of the increa  ...[more]

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