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dc.contributor.author
Yu, Zhan  
dc.contributor.author
Chen, Lee Chuin  
dc.contributor.author
Mandal, Mridul Kanti  
dc.contributor.author
Nonami, Hiroshi  
dc.contributor.author
Erra Balsells, Rosa  
dc.contributor.author
Hiraoka, Kenzo  
dc.date.available
2019-01-16T20:20:31Z  
dc.date.issued
2012-04  
dc.identifier.citation
Yu, Zhan; Chen, Lee Chuin; Mandal, Mridul Kanti; Nonami, Hiroshi; Erra Balsells, Rosa; et al.; Online electrospray ionization mass spectrometric monitoring of protease-catalyzed reactions in real time; Springer; Journal of The American Society for Mass Spectrometry; 23; 4; 4-2012; 728-735  
dc.identifier.issn
1044-0305  
dc.identifier.uri
http://hdl.handle.net/11336/68168  
dc.description.abstract
Although there are a lot of well established methods for monitoring enzyme-catalyzed reactions, most of them are based on changes in spectroscopic properties during the conversion of substrates to products. However, reactions without optical changes are common, which are inapplicable to these spectroscopic methods. As an alternative technique for enzymologic research, mass spectrometry (MS) is favored due to its specificity, sensitivity, and the ability to obtain stoichiometric information. In this work, probe electrospray ionization (PESI) source coupled with a time of flight mass spectrometer was employed to monitor some typical proteasecatalyzed reactions, including pepsinolysis and trypsinolysis of cytochrome c in real time. Due to the high electrical conductivity of each reaction system, corona discharges are likely to occur, which would decrease intensities of mass spectrometric signals. An ultra-fine sampling probe and an auxiliary vapor spray were adopted to prevent corona discharges. Experimental results from peptic and tryptic digestions of cytochrome c showed different and characteristic catalytic pathways. With the data presented in this study, PESI-MS can be considered as a potential tool for real-time monitoring of enzymatic reactions because of its simplicity in instrumental configuration, wide applicability under harsh conditions, and flexibility in combination with other techniques.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Springer  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Electrochemical Etching  
dc.subject
Onlinemonitoring  
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Probe Electrospray Ionization  
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Proteolytic Reactions  
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Solid Probe  
dc.subject.classification
Otras Ciencias Químicas  
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Ciencias Químicas  
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CIENCIAS NATURALES Y EXACTAS  
dc.title
Online electrospray ionization mass spectrometric monitoring of protease-catalyzed reactions in real time  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2019-01-16T18:10:56Z  
dc.journal.volume
23  
dc.journal.number
4  
dc.journal.pagination
728-735  
dc.journal.pais
Alemania  
dc.journal.ciudad
Berlin  
dc.description.fil
Fil: Yu, Zhan. Shenyang Normal University; China. University Of Yamanashi; Japón  
dc.description.fil
Fil: Chen, Lee Chuin. University Of Yamanashi; Japón  
dc.description.fil
Fil: Mandal, Mridul Kanti. University Of Yamanashi; Japón  
dc.description.fil
Fil: Nonami, Hiroshi. Ehime University; Japón  
dc.description.fil
Fil: Erra Balsells, Rosa. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Centro de Investigaciones en Hidratos de Carbono; Argentina  
dc.description.fil
Fil: Hiraoka, Kenzo. University Of Yamanashi; Japón  
dc.journal.title
Journal of The American Society for Mass Spectrometry  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/https://dx.doi.org/10.1007/s13361-011-0323-5  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://link.springer.com/article/10.1007%2Fs13361-011-0323-5