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Home arrow Health arrow Analysis of Protein Post-Translational Modifications by Mass Spectrometry


The authors acknowledge the financial support from the National Natural Science Foundation of China (Grant No. 81272798 and 81572278 to X.Z.), the Hunan Provincial Natural Science Foundation of China (Grant No. 14JJ7008 to X. Z.), and the Xiangya Hospital Funds for Talent Introduction (to X.Z.) and China “863” Plan Project (Grant No. 2014AA020610-1 to X. Z.).


APPD (3-R,4.S)-1-(4-(aminomethyl)phenylsulfonyl)pyrrolidine-3,4-diol

BSA bovine serum albumin

CID collision-induced dissociation

COFRADIC combined fractional diagonal chromatography

cPILOT combined precursor isotopic labeling and isobaric tagging

ECD electron capture dissociation

ESI electrospray ionization

ETD electron transfer dissociation

FT-ICR Fourier transform ion cyclotron resonance

IR infrared iTRAQ isobaric tags for relative and absolute quantification

LC liquid chromatography

LE1 leucine enkephalin

LE2 nitro-Tyr leucine enkephalin

LE3 d(5)-Phe-nitro-Tyr leucine enkephalin

MAD metastable atom-activated dissociation

MALDI matrix-assisted laser desorption/ionization

MS mass spectrometry

MS/MS tandem mass spectrometry

m/z mass-to-charge ratio

NTAC nitrotyrosine affinity column

  • 3NT 3-nitrotyrosine residue
  • 1D/2D one/two dimensional

OVA ovalbumin

PMF peptide mass fingerprint

SCX strong cation exchange

SRM selected reaction monitoring

TMT tandem mass tags

TNM tetranitromethane

TOF time of flight

2DE two-dimensional electrophoresis

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