Pages 441–448
doi: 10.1255/ejms.647 Rearrangements of transient neutral molecules in the gas phase. Does the
conversion of CCCHO to HCCCO involve oxygen or hydrogen migration? Khoa M. Tran, Andrew M. McAnoy and John H. Bowie*
Department
of Chemistry, The University of Adelaide, South Australia, 5005. E-mail: john.bowie@adelaide.edu.au
Pages 449–457
doi: 10.1255/ejms.648 A Comparative Study of the Collision Induced Dissociation and the Electron
Capture Dissociation of Model Peptides Using ESI-FTMS Y.M. Eva Fung, Lifang Duan and T.-W. Dominic Chan*
Department of Chemistry,
The Chinese University of Hong Kong, Shatin, NT, Hong Kong
Pages 459–468
doi: 10.1255/ejms.655 Liquid injection field desorption ionization: a new tool for soft ionization of samples
including air sensitive catalysts and non-polar hydrocarbons H. Bernhard Linden
Linden CMS GmbH, Auf dem Berge 25, D-28844 Leeste, Germany. E-mail:
linden@fdms.de
Pages 469–476
doi: 10.1255/ejms.654 High detection sensitivity achieved with cryogenic detectors in combination with
matrix-assisted laser desorption / ionisation time-of-flight mass spectrometry P. Christ,* S. Rutzinger, W. Seidel, S. Uchaikin and F.
Pröbst
Max Planck Institut für Physik, Föhringer Ring 6, 80805 München, Germany. E-mail: christ@mppmu.mpg.de
C. Koy and
M.O. Glocker
Proteome Center Rostock, Joachim-Jungius-Str. 9, 18059 Rostock, Germany
Pages 477–486
doi: 10.1255/ejms.650 The role of free electrons in MALDI: electron capture by molecules of α-
cyano-4-hydroxycinnamic acid S.A. Pshenichnyuk* and N.L. Asfandiarov
Institute of Physics of Molecules and Crystals, Ufa Research Center,
Russian Academy of Sciences, October Avenue 151, 450075 Ufa, Russia. E-mail: sapsh@anrb.ru
Pages 487–493
doi: 10.1255/ejms.645 Parameterising matrix-assisted laser desorption / ionization (MALDI): Effect of
solvents and co-additives on analyte peak intensities S. Bashir,a,c* R. Mutterb,d and P.J.
Derricka
aInstitute of Mass Spectrometry and Department of Chemistry, University of Warwick, Coventry CV4 7AL,
UK
bDepartment of Chemistry, University of Warwick, Coventry CV4 7AL, UK
Pages 495–500
doi: 10.1255/ejms.633 The abundances of fragment ions formed via skeletal rearrangements from 2,5-
disubstituted-1,3,4-oxadiazoles and their theoretical calculated stabilities Rafał Frański,a,* Krystian Eitner,a Grzegorz
Schroedera and Oles P. Szwajkab
aAdam Mickiewicz University, Faculty of Chemistry, Grunwaldzka 6, 60-780 Poznań,
Poland
bNational State University of Donetsk, Donetsk, Ukraine
Pages 501–508
doi: 10.1255/ejms.652 Mass spectrometry analysis of synthetically myristoylated peptides Tsefang S. Chen, Jennifer D. Yoder, and Dennis E. Hruby*
Department of Microbiology, Oregon State University, 220 Nash Hall, Corvallis, OR 97331-
3804, USA. E-mail: hrubyd@science.oregonstate.edu
Pages 509–521
doi: 10.1255/ejms.649 Low pressure chemical ionization in ion trap mass spectrometry Stéphane Bouchonnet,* Danielle Libong and Michel Sablier
Département de Chimie des Mécanismes Réactionnels,
Ecole Polytechnique, route de Saclay, 91128 Palaiseau Cedex, France. E-mail: stephane.bouchonnet@dcmr.polytechnique.fr
Pages 523–539
doi: 10.1255/ejms.658 Collision-induced dissociation of a series of coumarins studied by positive- and
negative-ion electrospray triple quadrupole tandem mass spectrometry Lidija Lerman, Andreja Čempuh Klonkay, Anita Filipović and Ivaylo
Elenkov*
Pliva, Research and Development, Zagreb, Croatia
Pages 541–554
doi: 10.1255/ejms.646 Structural reinvestigation of the core oligosaccharide of a mutant form of
Aeromonas salmonicida lipopolysaccharide containing an O-4 phosphorylated and O-5 substituted Kdo reducing end group using electrospray QqTOF-MS/MS Joseph Banoub,1,2* Alejandro Cohen,2 Anas El Aneed,2 Vincent LeQuart3 and Patrick
Martin3
1Department of Fisheries and Oceans, Science, Oceans and Environment Branch, Special Projects, PO Box 5667, St. John’s, NL
A1C 5X1, Canada
2Memorial University of Newfoundland, Biochemistry Department, St. John’s, NL A1C 5S7, Canada
3IUT Bethune,
Departement de Chimie, Université d’Artois, Bethune, France
Pages 555–568
doi: 10.1255/ejms.653 Review: Derivatization in mass spectrometry - 4. Formation of cyclic derivatives Vladimir G. Zaikin
Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Moscow, Russia. E-mail: zaikin@ips.ac.ru
John M.
Halket
Drug Control Centre, King's College London, Franklin-Wilkins Building, Stamford Street, London SE1 9NN, UK. E-mail: john.halket@kcl.ac.uk
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