EYER, Luděk, Roman PANTŮČEK, Zbyněk ZDRÁHAL, Hana KONEČNÁ, Petr KAŠPÁREK, Vladislava RŮŽIČKOVÁ, Lenka HERNYCHOVÁ, Jan PREISLER and Jiří DOŠKAŘ. Structural protein analysis of the polyvalent staphylococcal bacteriophage 812. Proteomics. Weinheim: Wiley-VCH, 2007, vol. 7, No 1, p. 64-72. ISSN 1615-9853.
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Basic information
Original name Structural protein analysis of the polyvalent staphylococcal bacteriophage 812
Name in Czech Analýza strukturních proteinů polyvalentního stafolofága 812
Authors EYER, Luděk (203 Czech Republic, belonging to the institution), Roman PANTŮČEK (203 Czech Republic, belonging to the institution), Zbyněk ZDRÁHAL (203 Czech Republic, belonging to the institution), Hana KONEČNÁ (203 Czech Republic, belonging to the institution), Petr KAŠPÁREK (203 Czech Republic), Vladislava RŮŽIČKOVÁ (203 Czech Republic, belonging to the institution), Lenka HERNYCHOVÁ (203 Czech Republic), Jan PREISLER (203 Czech Republic, belonging to the institution) and Jiří DOŠKAŘ (203 Czech Republic, guarantor).
Edition Proteomics, Weinheim, Wiley-VCH, 2007, 1615-9853.
Other information
Original language English
Type of outcome Article in a journal
Field of Study Genetics and molecular biology
Country of publisher Germany
Confidentiality degree is not subject to a state or trade secret
WWW [Abstract] [PDF]
Impact factor Impact factor: 5.479
RIV identification code RIV/00216224:14310/07:00020066
Organization unit Faculty of Science
UT WoS 000243762900007
Keywords in English staphylococcus bacteriophage; proteome; Myoviridae; Staphylococcus aureus; phage therapy
Tags Myoviridae, phage therapy, proteome, Staphylococcus aureus, Staphylococcus bacteriophage
Tags International impact, Reviewed
Changed by Changed by: prof. Mgr. Jan Preisler, Ph.D., učo 45329. Changed: 9/4/2013 14:18.
Abstract
Phage 812 is a polyvalent phage with a very broad host range in the genus Staphylococcus, which makes it a suitable candidate for phage therapy of staphylococcal infections. This proteomic study, combining the results of both 1-DE and 2-DE followed by PMF, led to the identification of 24 virion proteins. Twenty new proteins, not yet identified by proteome analysis of closely related staphylococcal phages K and G1 were identified using this approach. Fifteen proteins were assigned unambiguously to the head-tail genome module; the remaining nine proteins are encoded by genes of the left or right arms of the phage genome. As expected, the most abundant proteins in the electrophoretic patterns are the major capsid protein, the major tail sheath protein and proteins identical to ORF 50 and ORF 95 of phage K, although their function is only putative. Identification of these 20 new proteins contributes substantially to a detailed characterization of phage virions, knowledge of which is necessary for rational phage therapy
Abstract (in Czech)
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Links
GA203/03/0515, research and development projectName: Integrovaná analýza genomu a proteomu terapeuticky významných bakteriofágů kombinací elektroforézy a hmotnostní spektrometrie
Investor: Czech Science Foundation, Integrated genome and proteome analysis of therapeutically important bacteriophages by combination of electrophoresis and mass spectrometry
MSM0021622415, plan (intention)Name: Molekulární podstata buněčných a tkáňových regulací
Investor: Ministry of Education, Youth and Sports of the CR, Molecular basis of cell and tissue regulations
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