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- W4244580745 abstract "Abstract Nonvolatile salts are essential for the structures and functions of many proteins and protein complexes but can severely degrade performance of native mass spectrometry by adducting to protein and protein complex ions, thereby reducing sensitivity and mass measuring accuracy. Small nanoelectrospray emitters are used to form protein and protein complex ions directly from high‐ionic‐strength (>150 m m ) nonvolatile buffers with salts that mimic the extracellular environment. Charge‐state distributions are not obtained for proteins and protein complexes from six commonly used nonvolatile buffers and ≥150 m m Na + with conventionally sized nanoelectrospray emitter tips but are resolved with 0.5 μm tips. This method enables mass measurements of proteins and protein complexes directly from a variety of commonly used buffers with high concentrations of nonvolatile salts and eliminates the need to buffer exchange into volatile ammonium buffers traditionally used in native mass spectrometry." @default.
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- W4244580745 date "2017-06-05" @default.
- W4244580745 modified "2023-09-25" @default.
- W4244580745 title "Native Mass Spectrometry from Common Buffers with Salts That Mimic the Extracellular Environment" @default.
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- W4244580745 doi "https://doi.org/10.1002/ange.201702330" @default.
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