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2D FT-ICR MS of Calmodulin: A Top-Down and Bottom-Up Approach
被引:34
作者:
Floris, Federico
[1
]
van Agthoven, Maria
[1
]
Chiron, Lionel
[2
]
Soulby, Andrew J.
[1
]
Wootton, Christopher A.
[1
]
Lam, Yuko P. Y.
[1
]
Barrow, Mark P.
[1
]
Delsuc, Marc-Andre
[2
,3
]
O'Connor, Peter B.
[1
]
机构:
[1] Univ Warwick, Coventry, W Midlands, England
[2] CASC4DE, Illkirch Graffenstaden, France
[3] IGBMC, Illkirch Graffenstaden, France
基金:
英国工程与自然科学研究理事会;
关键词:
Tandem mass spectrometry;
FTICR mass spectrometry;
2-Dimensional mass spectrometry;
ION-CYCLOTRON RESONANCE;
INFRARED MULTIPHOTON DISSOCIATION;
MASS-SPECTROMETRY;
FRAGMENTATION PATHWAYS;
NOISE;
PEPTIDES;
D O I:
10.1007/s13361-016-1431-z
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Two-dimensional Fourier transform ion cyclotron resonance mass spectrometry (2D FT-ICR MS) allows data-independent fragmentation of all ions in a sample and correlation of fragment ions to their precursors through the modulation of precursor ion cyclotron radii prior to fragmentation. Previous results show that implementation of 2D FT-ICR MS with infrared multi-photon dissociation (IRMPD) and electron capture dissociation (ECD) has turned this method into a useful analytical tool. In this work, IRMPD tandem mass spectrometry of calmodulin (CaM) has been performed both in one-dimensional and two-dimensional FT-ICR MS using a top-down and bottom-up approach. 2D IRMPD FT-ICR MS is used to achieve extensive inter-residue bond cleavage and assignment for CaM, using its unique features for fragment identification in a less time- and sample-consuming experiment than doing the same thing using sequential MS/MS experiments.
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页码:1531 / 1538
页数:8
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