Collision-induced dissociation mass

Collision-induced dissociation mass spectrum of tire proton-bound dimer of isopropanol [(CH2)2CHOH]2H. The mJz 121 ions were first isolated in the trap, followed by resonant excitation of their trajectories to produce CID. Fragment ions include water loss mJz 103), loss of isopropanol mJz 61) and loss of 42 anui mJz 79). (b) Ion-molecule reactions in an ion trap. In this example the mJz 103 ion was first isolated and then resonantly excited in the trap. Endothennic reaction with water inside the trap produces the proton-bound cluster at mJz 121, while CID produces the fragment with mJz 61. 

Muller, C., Schafer, P., Stortzel, M., Vogt, S., and Weinmann, W. (2002). Ion suppression effects in liquid chromatography-electrospray-ionization transport-region collision induced dissociation mass spectrometry with different serum extraction methods for systematic toxicological analysis with mass spectra libraries. /. Chromatogr. B 773, 47— 52. 

Wang PP, Bartlett MG (1998) Collision-induced dissociation mass spectra of cocaine, and its metabolites and pyrolysis products. J Mass Spectrom 33 961-967... 

Muller, C. Schafer, R Stortzel,M. Vogt, S. Weinmann, W. Ion Suppression Effects in Liquid Chromatography-Electrospray-Ionisation Transport-Region Collision Induced Dissociation Mass Spectrometry with Different Serum Extraction Methods for Systematic Toxicological Analysis with Mass Spectra Libraries, J. Chromatogr. B Anal. Technol. Biomed. Life Sci. 773(1), 47-52 (2002). 

Flamini, R. and Dalla Vedova, A. (2004). Fast determination of the total free resveratrol content in wine by direct-exposure-probe, positive-ion chemical ionization and collision-induced-dissociation mass spectrometry, Rapid Commun. Mass Spectrom., 18,1925-1931. 

Deng, Y, Pan, H., Smith, D.L. (1999) Selective isotope labeling demonstrates that hydrogen exchange at individual peptide amide linkages can be determined by collision-induced dissociation mass spectrometry. J Am Chem Soc, 121 (9), 1966-1967. 

P. H. Lipniunas, R. R. Reid Townsend, A. L. Burhngame, and O. Hindsgaul, Fligh-energy collision-induced dissociation mass spectrometry of synthetic mannose-6-phosphate oligosaccharides, 7. Am. Soc. Mass Spectrom. 7,182-188 (1996). 

Rodgers MT, Armentrout PB. Noncovalent metal-ligand bond energies as studied by threshold collision-induced dissociation. Mass Spectrom Rev. 2000 19 215 7. 

Poon C, Kaplan H, Mayer PM. Methylating peptides to prevent adduct ion formation also directs cleavage in collision-induced dissociation mass spectrometry. Eur J Mass Spectrom. 

Field desorption - collision induced dissociation mass spectra of seven disaccharides, involving alkali metal-cationized... 

FIGURE 9.14 Collision-induced dissociation mass spectra of Qo, using helium as the target gas at (a) low [20%], (b) medium [80%] and (c) high [98%] attenuation. (Reprinted with permission from reference 11). 

Hines, W.M., Falick, A.M., Burlingame, A.L. and Gibson, B.W., Pattern-based algorithm for peptide sequencing from tandem high energy collision-induced dissociation mass spectra. J. Am. Soc. Mass Spectrom., 3, 326-336 (1992). 

Similar results were obtained by CID-MIKE (collision induced dissociation) mass spectrometry of an ornithine-containing lipid (57). Homologues were detected by FAB mass spectrometry and the ions were distinguished by their CID spectra (52). 

Figure 10 (A) Surface-induced dissociation spectrum of the pyrene molecular ion mlz202) with a stainless steel surface at a collision energy of 100 eV. (B) Collision-induced dissociation mass spectrum of the pyrene moelcular ion (miz 202) with Ar under single collision condiitons. Note that the mIz axis is not aligned or the same scale between (A) and (B). Adapted with permission fron Riederer Jr DE, PhD Thesis, Purdue University, 1993.

Figure 5 Collision induced dissociation mass spectra of (A) CHsOH and (B) CH20H2. Note the intense signal for the doubly charged ion in (B).

Nacson, S. Harrison, A. G. Davidson, W. R. Effect of Method of Ion Preparation on Low-Energy Collision-Induced Dissociation Mass Spectra. Org. Mass Spectrom. 1986, 21, 317 319. 

Gillece-Castro, B. L. Burlingame, A. L. Oligosaccharide Characterization with High-Eneigy Collision-Induced Dissociation Mass Spectrometry. Met. Enzy. 1990, 193, 689-712. 

M. Lisurek, M.-I. Kang, R.W. Hartmann, R. Bernhardt, Identification of monohydroxy pro-gesterones produced by CYP106A2 using comparative HPLC and electrospray ionisation collision-induced dissociation mass spectrometry, Biochem. Biophys. Res. Commun. 319 (2) (2004) 677-682. 

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