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Activated ion electron capture dissociation

Horn, D.M. Ge, Y. McLafferty, F.W. Activated ion electron capture dissociation for mass spectral sequencing of larger (42 kDa) proteins. Anal. Chem. 2000, 72, 4778-4784. [Pg.77]

Tsybin, Y. O. He, H. Emmett, M. R. Hendrickson, C. L. Marshall, A. G. Ion activation in electron capture dissociation to distinguish between N-terminal and C-terminal product ions. Anal. Chem. 2007, 79, 7596-7602. [Pg.626]

DGE a AC AMS APCI API AP-MALDI APPI ASAP BIRD c CAD CE CF CF-FAB Cl CID cw CZE Da DAPCI DART DC DE DESI DIOS DTIMS EC ECD El ELDI EM ESI ETD eV f FAB FAIMS FD FI FT FTICR two-dimensional gel electrophoresis atto, 10 18 alternating current accelerator mass spectrometry atmospheric pressure chemical ionization atmospheric pressure ionization atmospheric pressure matrix-assisted laser desorption/ionization atmospheric pressure photoionization atmospheric-pressure solids analysis probe blackbody infrared radiative dissociation centi, 10-2 collision-activated dissociation capillary electrophoresis continuous flow continuous flow fast atom bombardment chemical ionization collision-induced dissociation continuous wave capillary zone electrophoresis dalton desorption atmospheric pressure chemical ionization direct analysis in real time direct current delayed extraction desorption electrospray ionization desorption/ionization on silicon drift tube ion mobility spectrometry electrochromatography electron capture dissociation electron ionization electrospray-assisted laser desorption/ionization electron multiplier electrospray ionization electron transfer dissociation electron volt femto, 1CT15 fast atom bombardment field asymmetric waveform ion mobility spectrometry field desorption field ionization Fourier transform Fourier transform ion cyclotron resonance... [Pg.11]

The activation step can alternatively be performed without gas by means of infrared multiphoton dissociation (IRMPD) or electron capture dissociation (BCD) (Chap. 2.12.2). Both IRMPD and BCD, solely require storage of the ions during their excitation by photons or electrons, respectively. It is one of the most charming properties of FT-ICR-MS/MS that even the accurate mass of the fragment ions can be determined. [216,217]... [Pg.172]

FT-ICR instruments are also capable of performing MS" experiments. The most popular method of ion activation is sustained off-resonance irradiation (SORI), where ions are excited to a larger cyclotron radius using rf energy, undergo collisions with a neutral gas pulsed into the cell and dissociate. Other methods are available, including infrared multiphoton dissociation (IRMPD)65 and electron capture dissociation (ECD)66 which is of particular value in glyco-peptide analysis (Section VIA). [Pg.85]

Two other ion activation methods were developed to replace the gas molecules as targets by laser beams (photodissociation or infrared multiphoton dissociation IRMPD) or by electron beams (electron capture dissociation ECD). These two methods can be applied to ions that are trapped during their excitations by photons or electrons, respectively. Thus, they are most often used with ion trap or ICR analysers because the residence time and the interaction time are longer. [Pg.200]

Electron capture dissociation (ECD) has recently been developed as an alternative activation method and is now widely used [24,25], The ECD activation method is applied to multiply charged positive ions submitted to a beam of low energy produced by an emitter... [Pg.200]

The fragmentation of peptides can also be obtained by FTICR instruments. Besides the most commonly used activation method, namely CID, the activation can alternatively be performed without gas by infrared multiphoton dissociation (IRMPD) and electron capture dissociation (ECD). These methods fragment peptide ions in the ICR cell by emitting a laser beam or electron beam, respectively. [Pg.310]

The following ion-activation techniques have been used at one time or other to sequence peptides (1) fast atom bombardment (FAB) ionization, (2) CID—tandem MS (MS/MS), (3) ESI in-source CID, (4) MALDI ion-source decay, (5) MALDI postsource decay (PSD), (6) electron-capture dissociation (ECD) and electron-transfer dissociation, and (7) peptide ladder sequencing. Because of the lack of space, only (2) and (4) will be discussed further. [Pg.473]

Electron-Capture Dissociation (ECD) BCD mass spectmm can also identify the glycosylated sites in peptides. In this mild activation process, the carbohydrate chains remain attached to the sequence-specific c- and z-type ions, thereby providing direct evidence of glycosylation in glycosylated peptides [85]. [Pg.369]

In addition, new tandem mass spectrometry technologies were also among the important innovations. Apart from traditional collision-induced dissociation (CID) [89-91], a variety of activation methods (used to add energy to mass-selected ions) based on inelastic collisions and photon absorption have been widely utilized. They include IR multiphoton excitation [92,93], UV laser excitation [94—97], surface-induced dissociation (SID) [98-100], black body radiation (101, 102], thermal dissociation [103], and others. As the fragmentation of peptide/protein ions is a central topic in proteomics, there is strong interest in such novel ion dissociation methods as electron capture dissociation (ECD) [104, 105] and electron transfer dissociation [22]. These new methods can provide structural information that complements that obtained by traditional collisional activation. Also, very recently, ambient ion dissociation methods such as atmospheric pressure thermal dissociation [106] and low temperature plasma assisted ion dissociation [107] have been reported. [Pg.41]

While most peptide dissociation is carried out in the positive ion mode, the negative ion mode is often better suited for acidic peptides, particularity those carrying acidic modifications (e.g., phosphorylations). There are a number of equivalent ion activation methods for peptide anions, involving ion-electron and ion-ion reactions, such as electron detachment dissociation (EDD) [49], negative electron transfer dissociation (NETD) [50, 51], and negative electron capture dissociation (nECD) [52]. [Pg.178]

Following the development of the hybrid Q-FTMS instruments, a linear ion trap (LIT) was used in place of the mass-filtering quadrupole and storage multipole. This hybrid-FTMS configuration is found in some commercial FTMS instruments, and an example of this instrument configuration is shown in Figure 11.20C. Ions pass from the ESI source into the LIT where they are stored, and then they are passed down to the analyzer cell. With the LIT, ion accumulation, mass selection, and dissociation (including MS") can be performed within the LIT instead of the analyzer cell. CAD is typically performed within the LIT, while other methods of ion activation, infrared multiphoton dissociation (IRMPD), and electron capture dissociation (ECD) (vide infra) are performed inside the analyzer cell. One unique... [Pg.391]

Dissociative electron capture is observed with hyperthermal electrons in NIMS electron impact experiments. In order for dissociative electron capture to take place with thermal electrons, there must be a dissociative pathway that is accessible by the thermal activation of the neutral molecule or a low-lying negative-ion state. The quantity D(R — Le) — Ea(Le) must be less than about 1.0 eV. This limit has been established empirically. Two types of dissociative thermal electron attachment have been observed in NIMS and ECD. The first occurs by unimolecular dissociation in which there is only one temperature region for many compounds. In the original work a low-temperature low-slope region was observed but unexplained. We now believe this could represent the formation of a molecular ion with an electron affinity of about 0.1 eV. The exact nature of this ion is not known, but it could represent stabilization to an excited state. In Figure 4.8 ECD data are plotted for several... [Pg.59]


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Activated dissociation

Activation electronic

Dissociation, Ions

Dissociative electron capture

Electron activation

Electron dissociation

Electron dissociative

Electronic dissociative

Electrons active

Ion activity

Ion-activated

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