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  • 1
    Online Resource
    Online Resource
    Newark :John Wiley & Sons, Incorporated,
    Keywords: Matrix-assisted laser desorption-ionization. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (477 pages)
    Edition: 2nd ed.
    ISBN: 9783527673735
    Language: English
    Note: Cover -- Related Titles -- Title page -- Copyright page -- Contents -- Preface to the Second Edition -- List of Contributors -- 1: The MALDI Process and Method -- 1.1 Introduction -- 1.2 Analyte Incorporation -- 1.3 Absorption of the Laser Radiation -- 1.4 The Ablation/Desorption Process -- 1.5 Ionization -- 1.6 Fragmentation of MALDI Ions -- 1.7 MALDI of Noncovalent Complexes -- 1.8 The Optimal Choice of Matrix: Sample Preparation -- 1.8.1 Surface Preparation -- 1.8.2 Anchor Sample Plates -- 1.8.3 Matrix Additives and Influence of the Sample Plate Surface -- Abbreviations -- References -- 2: MALDI Mass Spectrometry Instrumentation -- 2.1 Introduction -- 2.2 Lasers for MALDI-MS -- 2.3 Fragmentation of MALDI Ions -- 2.3.1 MALDI at Elevated Pressure -- 2.3.2 Tandem Mass Spectrometry of MALDI Ions -- 2.4 Mass Analyzers -- 2.4.1 Axial TOF Mass Spectrometers -- 2.4.2 Reflectron TOF Mass Spectrometers -- 2.4.3 Tandem TOF Mass Spectrometers -- 2.4.4 Orthogonal TOF Mass Analyzers -- 2.4.5 Tandem Mass Spectrometry in oTOF Mass Analyzers -- 2.4.6 Ion Detectors and Data Processing in MALDI-TOF Analyzers -- 2.5 Fourier Transform Ion Cyclotron Resonance Mass Spectrometers -- 2.5.1 Tandem Mass Spectrometry on FTICR Mass Spectrometers -- 2.6 Quadrupole Ion Trap Mass Spectrometers -- 2.6.1 RF-Only Ion Guides and LIT Mass Spectrometers -- 2.6.2 Tandem Mass Spectrometry on QIT Mass Spectrometers -- 2.7 Hybrid Mass Spectrometers -- 2.7.1 Quadrupole TOF Mass Spectrometers -- 2.7.2 Quadrupole FT Mass Spectrometers -- 2.7.3 QIT-TOF Mass Spectrometers -- 2.7.4 Ion Mobility oTOF Mass Spectrometers -- 2.7.5 Orbitrap -- 2.8 Future Directions -- Definitions and Acronyms -- References -- 3: MALDI-MS in Protein Chemistry and Proteomics -- 3.1 Introduction -- 3.2 Sample Preparation for Protein and Peptide Analysis by MALDI-MS. , 3.3 Strategies for Using MALDI-MS in Protein Biochemistry -- 3.3.1 Peptide Mass Mapping of Purified Proteins -- 3.3.2 Peptide Sequencing by MALDI-MS/MS -- 3.3.3 Analysis of Post-Translational Modifications -- 3.4 Applications of MALDI-MS in Proteomics -- 3.4.1 Protein Identification by MALDI-MS Peptide Mass Mapping -- 3.4.2 Quantitation of Proteins by MALDI-MS -- 3.5 Computational Tools for Protein Analysis by MALDI-MS -- 3.6 Clinical Applications of MALDI-MS -- 3.7 Conclusions -- Acknowledgments -- References -- 4: MALDI-Mass Spectrometry Imaging -- 4.1 Introduction -- 4.2 History of Mass Spectrometry Imaging (MSI) and Microprobing Techniques -- 4.3 MALDI in Micro Dimensions: Instruments and Mechanistic Differences -- 4.4 Visualization of Mass Spectrometric Information -- 4.5 Data Processing and Data Exchange -- 4.6 Matrix Deposition for High-Resolution Imaging -- 4.7 Organisms, Organs, and Tissues: MALDI Imaging at Various Lateral Resolutions -- 4.7.1 Phospholipid Analysis -- 4.7.2 Peptide Analysis -- 4.7.3 Drug Monitoring -- 4.8 Whole-Cell and Single-Cell Analysis -- 4.8.1 Cellular Analysis -- 4.8.2 Individually Isolated Cells -- 4.8.3 Direct Cellular and Subcellular Imaging -- 4.9 Cell Sorting and Capturing -- 4.10 Direct Protein Identification and Localization -- 4.11 Identification and Characterization: Requirements for Mass Resolution and Accuracy -- 4.12 Conclusions -- Acknowledgments -- References -- 5: Analysis of Nucleic Acids, and Practical Implementations in Genomics and Genetics -- 5.1 Challenges in Nucleic Acid Analysis by MALDI-MS -- 5.2 Genetic Markers -- 5.2.1 Restriction Fragment Length Polymorphisms (RFLPs) -- 5.2.2 Microsatellites/Short Tandem Repeats (STRs) -- 5.2.3 Single Nucleotide Polymorphisms (SNPs) -- 5.2.4 Characterization of Base Modifications and Covalent Adducts. , 5.2.5 Detection of Noncovalent Complexes of Nucleic Acids -- 5.3 Assay Formats for Nucleic Acid Analysis by MALDI-MS -- 5.4 Applications in Genotyping -- 5.4.1 MALDI-TOF-MS SNP and Mutation Analysis -- 5.4.2 MALDI-TOF MS for Haplotyping -- 5.5 Applications in Comparative Sequence Analysis -- 5.6 Applications in Quantitation of Nucleic Acids for Analysis of Gene Expression and Gene Amplification -- 5.6.1 Analysis of DNA Mixtures and Allele Frequency Determinations in DNA Pools -- 5.6.2 Analysis of Gene Expression -- 5.7 Future Perspectives for the MALDI-MS Analysis of Nucleic Acids -- Acknowledgments -- References -- 6: MALDI-MS of Glycans and Glycoconjugates -- 6.1 Introduction -- 6.1.1 Glycans in Glycoproteins: Types and Importance -- 6.1.2 Glycosphingolipids -- 6.2 Profiling of Glycans and Glycosphingolipids -- 6.2.1 Importance of Glycan Profiling and Techniques Used for This Purpose -- 6.2.2 Importance of Glycosphingolipid Profiling and Characterization -- Techniques Used -- 6.2.3 MALDI-MS of Glycans and Glycoprotein Components -- 6.2.4 N- and O-Glycan Release -- 6.2.5 Preparation of Glycans for MALDI-MS Analysis -- 6.2.6 Preparation of Glycosphingolipids for MALDI-MS Analysis -- 6.3 Structural Determination -- 6.3.1 MS and MS/MS of N-Glycans -- 6.3.2 O-Glycosylation by MS and MS/MS -- 6.3.3 Exoglycosidase Arrays -- 6.3.4 Characterization of Glycopeptides -- 6.4 Quantitative Analysis -- 6.4.1 Quantitative Analysis of Glycans -- 6.4.2 Quantitative Analysis of Glycopeptides (e.g., i-Tag, i-Traq) -- 6.5 Conclusions -- References -- 7: Lipids -- 7.1 Introduction -- 7.1.1 Why Are Lipids of Such Great Interest? -- 7.1.2 Problems in Lipid Analysis: A Short Comparison of the Different Methods -- 7.1.3 Analysis of Lipids by Mass Spectrometry -- 7.1.4 Capabilities and Limitations of MALDI-TOF-MS in the Field of Lipid Analysis. , 7.1.5 Choosing an Appropriate Matrix -- 7.1.6 Sample Preparation, Extraction, and Purification -- 7.2 Analysis of Individual Lipid Classes and Their Characteristics -- 7.2.1 The Apolar Lipids: Diacylglycerols, Triacylglycerols, Cholesterol, and Cholesteryl Esters -- 7.2.2 Zwitterionic Phospholipids: Sphingomyelin, Phosphatidylcholine, and Phosphatidylethanolamine -- 7.2.3 Acidic Phospholipids: Phosphatidic Acid, Cardiolipin, Phosphatidylglycerol, Phosphatidylserine, Phosphatidylinositol, and Phosphorylated Phosphoinositides -- 7.2.4 Free Fatty Acids -- 7.3 MALDI-TOF-MS of Typical Lipid Mixtures -- 7.3.1 Brain Lipids -- 7.4 Characterization of Typical Oxidation Products of Lipids -- 7.5 MALDI-MS Imaging -- 7.6 Combining TLC and MALDI for Lipid Analysis -- 7.7 Summary and Outlook -- Acknowledgments -- Abbreviations -- References -- 8: MALDI-MS for Polymer Characterization -- 8.1 Introduction -- 8.2 Technical Aspects of MALDI-MS -- 8.2.1 Sample Preparation Issues -- 8.2.2 Instrumental and Measurement Issues -- 8.2.3 Data Processing Issues -- 8.3 Attributes and Limitations of MALDI-MS -- 8.4 Conclusions and Perspectives -- References -- 9: Small-Molecule Desorption/Ionization Mass Analysis -- 9.1 Introduction -- 9.2 Matrix Choices for Small-Molecule MALDI -- 9.2.1 Organic Matrices -- 9.2.2 Inorganic Matrices -- 9.2.3 Liquid Matrices -- 9.2.4 Matrix-Free Approaches -- 9.3 Sample Preparation -- 9.3.1 Electrospray Sample Deposition -- 9.3.2 Analyte Derivatization -- 9.3.3 Analyte Pre-Concentration -- 9.3.4 Matrix Suppression -- 9.4 Qualitative Characterization of LMM Molecules -- 9.5 Analyte Quantitation by MALDI -- 9.5.1 Selection of IS -- 9.5.2 Methods for Improving Quantitative Performance -- 9.5.3 Quantitation of Pharmaceutical Compounds -- 9.5.4 Enzyme Activity and Inhibition Studies. , 9.5.5 Quantitative Analysis of Samples from Complex Biological Matrices -- 9.5.6 Environmental Applications of Quantitative MALDI -- 9.5.7 Separation Methods Coupled with MALDI and DIOS -- 9.5.8 TLC-MALDI -- 9.5.9 Capillary and Frontal Affinity Liquid Chromatography -- 9.6 Conclusions -- Acknowledgments -- Abbreviations/Acronyms -- References -- 10: Computational Analysis of High-Throughput MALDI-TOF-MS-Based Peptide Profiling -- 10.1 Introduction -- 10.2 MALDI-MS Data Preprocessing -- 10.2.1 A Workflow for Data Acquired on a 4800 MALDI-TOF/TOF Mass Spectrometer -- 10.2.2 Identification of Peptide Ion Peaks -- 10.3 Statistical Analysis of Preprocessed Data -- 10.3.1 Unsupervised Methods -- 10.3.2 Supervised Methods -- 10.4 Concluding Remarks -- References -- 11: Biotyping of Microorganisms -- 11.1 The Technique -- 11.2 Standard Identification of Bacteria and Other Microorganisms -- 11.3 Applicability and Performance in Routine Laboratories -- 11.4 Direct Specimen Analysis -- 11.5 Subtyping -- 11.6 Resistance Testing -- 11.7 Outlook -- References -- Index.
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Biochemistry 28 (1989), S. 2923-2929 
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 46 (1981), S. 940-948 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-0843
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Intracellular concentrations of prednimustine (PM), chlorambucil (CLB), phenylacetic acid mustard (PAAM) and prednisolone (P) were measured in different experimental tumor cell lines that had been incubated with either PM or CLB+P. For intracellular analytical determination, we modified a high-pressure liquid chromatographic method for the detection of these substances in plasma. Intact PM could be detected in the intracellular compartment of the incubated tumor cells. PM-incubated cells from PM-injected rats exhibited a higher intracellular concentration-time integral (PAAM) and longer concentration-time profiles for drugs with alkylating capacity than did cells exposed to the CLB+P mixture or to CLB. PAAM was not detectable after incubation of cells with PM, whereas in CLB-incubated cells the AUC of PAAM exceeded that of the parent drug CLB. Our in vitro results therefore favour the concept of a facilitated intracellular uptake and an increased antiproliferative effect for PM versus CLB and CLB+P.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1573-4986
    Keywords: Gangliosides ; human granulocytes ; TLC overlay assay ; receptor ; influenza A virus ; Sendai virus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The structures of gangliosides from human granulocytes were elucidated by fast atom bombardment mass spectrometry and by gas chromatography/mass spectrometry as their partially methylated alditol acetates. In human granulocytes besides GM3 (II3Neu5Ac-LacCer), neolacto-series gangliosides (IV3Neu5Ac-nLcOse4Cer, IV6Neu5Ac-nLcOse4Cer and VI3Neu5Ac-nLcOse6Cer) containing C24:1, and to some extent C22:0; and C16:0 fatty acid in their respective ceramide portions, were identified as major components. In this study we demonstrate that gangliosides from human granulocytes, the second most abundant cells in peripheral blood, can serve as receptors for influenza viruses A/PR/8/34 (H1N1), A/X-31 (H3N2), and a parainfluenza virus Sendai virus (HNF1, Z-strain). Viruses were found to exhibit specific adhesion to terminal Neu5Acα2-3Gal and/or Neu5Acα2-6Gal sequences as well as depending on the chain length of ganglioside carbohydrate backbones from human granulocytes, these important effector cells which represent the first line of defence in immunologically mediated reactions.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1573-4986
    Keywords: O-linked glycans ; acidic carbohydrates ; mucins ; human milk ; FAB mass spectrometry ; NMR spectroscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract O-Linked glycans were isolated from human skim milk mucins or mucin-derived high-molecular weight glycopeptides and fractionated by anion exchange chromatography into neutral and acidic alditols. Major oligosaccharides contained in the acidic fraction were purified by high performance liquid chromatography and structurally characterized by a combination of fast atom bombardment mass spectrometry, methylation analysis and 500 MHz1H-nuclear magnetic resonance spectroscopy. The structural aspects exhibited by these major species in the acidic fraction resemble those established previously for the neutral oligosaccharides from human skim milk mucins: 1) the size of the alditols varies from tri- to decasaccharides 2) the core structure is of the ubiquitous type 2 3) the backbone sequences are of the poly-N-acetyllactosamine type with a particular preponderance of linearly extended GlcNAcβ(1–3)Gal (major) or GlcNAcβ(1–6)Gal units (minor). N-Acetylneuraminic acid on monosialylated (mucin- or glycopeptide-derived) and disialylated glycans (glycopeptide derived) is linked predominantly to position C-3 of galactose.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1573-0778
    Keywords: Hybridoma growth ; inhibition ; gangliosides ; GM 3
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Gangliosides of the mouse-rat hybridoma cell line 187.1, which secretes an antibody against ϰ-light chain of mouse IgG, were isolated and structurally characterized by biochemical and immunological methods (overlay technique), and fast atom bombardment-mass spectrometry. Exclusively G M3, substituted with C24∶1 and C16∶0 fatty acid and C18∶1 sphingosine, was found in this B cell derived cell line. A G M3 (NeuGc) to G M3(NeuAc) ratio (80 to 20), was characteristic for 187.1 cells, and absolute G M3 amounts of about 0.3 mg 10−9 viable cells were determined. Exogenous application of G M3, which has been isolated from large cell preparations, to 187.1 cells showed growth inhibition in a concentration dependent manner. Using the MTT-assay and the [3H]thymidine incorporation assay, the cells exhibited a strong reduction in metabolic and proliferative activity, respectively, after exposure of cells to G M3. G M3 was applied in concentrations between 3μM and 30μM, giving evidence for strong inhibitory effects at 30μM G M3 and less but significant suppression after application of G M3 concentrations lower than 20μM. No cellular response was observed at the lowest concentration (3μM) used in this study. Hybridoma cells as well as other cell types like fibroblasts, muscle cells and endothelial cells, are in general characterized by high expression of the G M3 ganglioside, which is known to act as a modulator of cellular growth in monolayer cultures of adherent cells. Since gangliosides are released to the culture medium by cell lysis, i.e. cell death, and/or by active membrane shedding, the results obtained in this study suggest a growth regulatory role of G M3 in high density hybridoma cell cultures.
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  • 10
    ISSN: 1573-4986
    Keywords: MDAY-D2 ; metastatic tumour cell line ; GD1α ; FAB-MS ; GC-MS
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The aim of the present study was to investigate the ganglioside expression of the highly metastatic murine lymphoreticular tumour cell line MDAY-D2. Cells were propagated under controlled pH conditions and oxygen supply in bioreactors of 1 and 7.5l volumes by repeated batch fermentation. Gangliosides were isolated from 2.7×1011 cells, purified by silica gel chromatography and separated into mono- and disialoganglioside fractions by preparative DEAE anion exchange high performance liquid chromatography. Individual gangliosides were obtained by preparative thin layer chromatography. Their structural features were established by immunostaining, fast atom bombardment and gas chromatography mass spectrometry. In addition to gangliosides of the GM1a-pathway (GM2, GM1a and GD1a) and GM1b (IV3Neu5Ac-GgOse4Cer) and GalNAc-GM1b of the GM1b-pathway, the dis8aloganglioside GD1α (IV3Neu5Ac, III6Neu5Ac-GgOse4Cer) was found in equal amounts compared to GD1a (IV3Neu5Ac, II3Neu5Ac-GgOse4Cer). All gangliosides were substituted with C24:0,24:1 and C16:0 fatty acids, sphingosine andN-acetylneuraminic acid as the sole sialic acid.
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