Detailed Information on Publication Record
2003
Proteomic Analysis of Therapeutically Important Bacteriophage 812 by Combination of Electrophoresis and Mass Spectrometry
PREISLER, Jan, Zbyněk ZDRÁHAL, Karel KLEPÁRNÍK, František FORET, Patrik VRÁBEL et. al.Basic information
Original name
Proteomic Analysis of Therapeutically Important Bacteriophage 812 by Combination of Electrophoresis and Mass Spectrometry
Authors
PREISLER, Jan (203 Czech Republic, guarantor), Zbyněk ZDRÁHAL (203 Czech Republic), Karel KLEPÁRNÍK (203 Czech Republic), František FORET (203 Czech Republic), Patrik VRÁBEL (203 Czech Republic), Zdena MALÁ (203 Czech Republic), Jiří DOŠKAŘ (203 Czech Republic), Roman PANTŮČEK (203 Czech Republic), Vladislava RŮŽIČKOVÁ (203 Czech Republic), Hana KONEČNÁ (203 Czech Republic) and Pavel KRÁSENSKÝ (203 Czech Republic)
Edition
Montreal, Proceedings of the 51st Annual Conference on Mass Spectrometry and Allied Topics, p. 1152-1152, 2003
Publisher
American Society for Mass Spectrometry
Other information
Language
English
Type of outcome
Stať ve sborníku
Field of Study
Genetics and molecular biology
Country of publisher
Canada
Confidentiality degree
není předmětem státního či obchodního tajemství
RIV identification code
RIV/00216224:14310/03:00008100
Organization unit
Faculty of Science
Keywords in English
MALDI; staphylococcal bacteriophage; proteome
Změněno: 3/3/2006 14:34, prof. Mgr. Jan Preisler, Ph.D.
Abstract
V originále
The alarming increase in antibiotic-resistant bacteria has renewed interest in bacteriophage therapy of various human infections, such as postoperative staphylococcal wound infections or anthrax. Genetic engineering has been previously applied for obtaining phage mutants with the desired host specificity. However, the genomic sequence similarity of the different phages is generally low, and identification of proteins with the same function in various phages based solely on the DNA sequence is often impossible. Furthermore, amino acid modifications, such as variants and post-translational modifications of the predicted proteins cannot be deduced from the DNA sequence. In this work, we propose new approaches to the analysis of the phage proteins, especially low abundant proteins, such as lytic enzymes. SDS gel electrophoresis was used for the protein separation followed by tryptic digestion and ESI or MALDI analysis. Additionally, protein and peptide separations were performed with capillary electrophoresis (CE) and a new universal interface has been developed to couple CE with MALDI MS.
Links
GA203/03/0515, research and development project |
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MSM 143100008, plan (intention) |
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