^*Indicates author to whom correspondence should be addressed

Vladimír Hanuš—an Appreciation

Vladimír Havlícek
Institute of Microbiology, Academy of Sciences of the Czech Republic, Vídeñská 1083, CZ-142 20 Prague 4, Czech Republic.

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DOI: 10.1255/ejms.224

Mass spectrometry of clusters: a new trend paralleling the development of biochemical mass spectrometry

István Cornides
Physics Department, Faculty of Science, Constantin Philosopher University, Tr. A. Hlinku 1, 949 74 Nitra, Slovakia.

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DOI: 10.1255/ejms.226

Energy partitioning in collisions of slow polyatomic ions with surfaces: ethanol molecular ions on stainless steel surfaces

Jirí Kubišta, Zdenìk Dolejšek and Zdenìk Herman
J. Heyrovský Institute of Physical Chemistry, Academy of Sciences of the Czech Republic, Dolejškova 3, 182 23 Prague 8, Czech Republic.

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DOI: 10.1255/ejms.227

Distinction of isomeric pyridyl cations and radicals by neutralization-reionization mass spectrometry, ab initio and density functional theory calculations

František Turecek, Jill K. Wolken and Martin Sadilek
Department of Chemistry, Bagley Hall, Box 351700, University of Washington, Seattle, WA 98195-1700, USA.

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DOI: 10.1255/ejms.228

Unimolecular dissociation of ionized methylcyclohexane

Tino Gäumann, Andreas Heusler, Sophie Haebel and Wei-Qing Feng
Institute of Physical Chemistry of the Federal School of Technology, Lausanne, Switzerland.

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DOI: 10.1255/ejms.229

The gas-phase reactions of the methoxymethyl cation with aldehydes and ketones

G. van der Rest, G. Bouchoux, H.E. Audier
Laboratoire des Mecanismes Réactionnels, CNRS UMR 7651, Ecole Polytechnique, 91128, Palaiseau, France.
T.B. McMahon
Department of Chemistry, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada.

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DOI: 10.1255/ejms.230

Proton affinity of some substituted 2,6-dimethylbenzamides and their N,N-dimethyl derivatives: the susceptibility of the amide group to polar substituent effects

Hans-Friedrich Grützmacher and Anke Caltapanides
Fakultät für Chemie der Universität Bielefeld, POB. 10 01 31, D-33501 Bielefeld, Germany.

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DOI: 10.1255/ejms.231

Low-energy collision induced dissociation of protonated peptides. Importance of an oxazolone formation for a peptide bond cleavage

Tomáš Vaisar and Jan Urban
Molecumetics Ltd, 2023 120^th Ave NE, Bellevue WA, USA. E-mail: tvaisar@molecumetics.com.

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DOI: 10.1255/ejms.233

Electrospray and atmospheric pressure chemical ionisation of aromatic compounds in dichloromethane solvent

Zoltán Takáts and Károly Vékey
Institute of Chemistry, Hungarian Academy of Sciences, H-1025 Budapest, Pusztaszeri út 59–67, Hungary.

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DOI: 10.1255/ejms.234

High performance liquid chromatography/ electrospray ionisation and atmospheric pressure chemical ionisation mass spectrometry for the analysis of butylated amino resins

Donata Favretto
CNR Area di Ricerca, Corso Stati Uniti 4, I-35100 Padova, Italy.
Pietro Traldi
CNR, Centro di Studi sulla Stabilita’ e Reattivita’ dei Composti di Coordinazione, Via Marzolo 1, I-35100 Padova, Italy.
Adriano Marcelli
McWorther, Sant’Albano Stura, Cuneo, Italy.

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DOI: 10.1255/ejms.235

p-Nitroaniline/glycerol: a binary liquid matrix for MALDI analysis

Tracie L. Williams and Catherine Fenselau^*
Department of Chemistry and Biochemistry, University of Maryland, College Park, MD 20742-2021, USA.

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DOI: 10.1255/ejms.236

Mass spectrometric amino acid structure determination in ergopeptines

Petr Halada, Petr Sedmera and Vladimír Havlícek^*
Institute of Microbiology, Academy of Sciences of the Czech Republic, Vídenská 1083, 142 20 Prague 4, Czech Republic. E- mail: vlhavlic@biomed.cas.cz
Alexandr Jegorov
Galena Co., Research Unit, Branišovská 31, 370 05 Ceské Budejovice, Czech Republic.
Ladislav Cvak
Galena Co., R&D, 747 70 Opava-Komárov, Czech Republic.
Miroslav Ryska
Prague Institute of Chemical Technology, Technická 5, Prague 6, Czech Republic.

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DOI: 10.1255/ejms.237

Linoleic acid peroxidation products are metabolized by hydrogenation in porcine liver tissue

Stefan Hecht and Gerhard Spiteller^*
Lehrstuhl Organische Chemie I, Universität Bayreuth, Universitätsstrasse 30, 95447 Bayreuth, Germany.

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DOI: 10.1255/ejms.238

Evaluation of heat-induced conformational changes in proteins by nanoelectrospray Fourier transform ion cyclotron resonance mass spectrometry

Thilo A. Fligge and Michael Przybylski^*
Fakultät für Chemie, Universität Konstanz, M 731, D-78457 Konstanz, Germany.
John P. Quinn and Alan G. Marshall
National High Magnetic Field Laboratory, Florida State University, 1800 East Paul Dirac Drive, Tallahassee, FL 32310, USA.

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DOI: 10.1255/ejms.239

Characterisation of genetically modified nisin molecules by Fourier transform ion cyclotron resonance mass spectrometry

Hélène Lavanant, Albert Heck and Peter J. Derrick
Institute of Mass Spectrometry and Department of Chemistry, University of Warwick, Coventry CV4 7AL, UK.
Fred A. Mellon,^* Adrian Parr, Helen M. Dodd, Catriona J. Giffard, Nikki Horn and Mike J. Gasson
Institute of Food Research, Norwich Laboratory, Norwich Research Park, Norwich NR4 7UA, UK. E-mail: fred.mellon@bbsrc.ac.uk.

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DOI: 10.1255/ejms.240

Letter: Matrix-assisted laser desorption/ionization and electrospray ionization mass spectrometry: sodium-cationized oligosaccharides do not exhibit “internal-residue loss” rearrangement

Vladimír Kovácik and Vladimír Pätoprstý
Institute of Chemistry, Slovak Academy of Sciences, Dúbravská cesta 9, 842 38 Bratislava, Slovak Republic.
Vladimír Havlicek
Institute of Microbiology, Academy of Sciences of the Czech Republic, Videñská 1083, 142 20 Prague, Czech Republic.
Pavol Kovác
NIDDK, National Institute of Health, Bethesda, Maryland 20892, USA.

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DOI: 10.1255/ejms.241

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