Download e-book for kindle: BSL3 and BSL4 Agents: Proteomics, Glycomics, and by Jiri Stulik, Rudolf Toman, Patrick Butaye, Robert G. Ulrich

By Jiri Stulik, Rudolf Toman, Patrick Butaye, Robert G. Ulrich

ISBN-10: 3527327800

ISBN-13: 9783527327805

Edited by means of major specialists within the ecu and the USA, this publication presents a distinct insurance of novel expertise methods for the detection of hugely similar versions of harmful brokers and novel treatment techniques. essential for all pros facing BSL3 and/or BSL four brokers

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Extra info for BSL3 and BSL4 Agents: Proteomics, Glycomics, and Antigenicity

Example text

The primary difference is in the reduced flow rate of the analyte containing liquid (μl/min and nl/min, respectively); this allows the application of micro- or nanoscale chromatography that yield much wanted sensitivity in proteomic experiments. This change causes adjustments in setup such as the reduced internal diameter of the tubing or lack of nebulization gas. 1). In the context of proteomics, its key parameters are sensitivity, resolution, mass accuracy and ability to generate information-rich ion mass spectra from peptides (MS/MS spectra).

The proteins can be identified either by peptide mass fingerprinting (PMF) or by peptide sequencing. 2 Peptide Mass Fingerprinting PMF is an analytical technique for protein identification [14–18]. A necessary condition of this method is the known genome of the analyzed organism. The unknown protein of interest is first experimentally cleaved into smaller peptides, whose absolute masses can be accurately measured with a mass spectrometer [19]. These masses are then in silico compared to either a database containing known protein or the gene sequences.

Chromatogr. A, 954, 115–126. , and Tempst, P. (1999) Immobilized gallium(III) affinity chromatography of phosphopeptides. Anal. , 71, 2883–2892. , et al. (2007) 48 49 50 51 52 53 54 55 56 57 Immobilized zirconium ion affinity chromatography for specific enrichment of phosphopeptides in phosphoproteome analysis. Mol. Cell. Proteomics, 6, 1656–1665. , and Aebersold, R. (2004) Chemical probes and tandem mass spectrometry, a strategy for the quantitative analysis of proteomes and subproteomes. Curr. Opin.

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BSL3 and BSL4 Agents: Proteomics, Glycomics, and Antigenicity by Jiri Stulik, Rudolf Toman, Patrick Butaye, Robert G. Ulrich


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