Real-time reaction monitoring by probe electrospray ionization mass spectrometry

Probe electrospray ionization (PESI) is a modified version of the electrospray ionization (ESI), where the capillary for sampling and spraying is replaced by a solid needle. High tolerance to salts and direct ambient sampling are major advantages of PESI compared with conventional ESI. In this study...

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Autor principal: Yu, Z.
Otros Autores: Chen, L.C, Erra-Balsells, R., Nonami, H., Hiraoka, K.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2010
Acceso en línea:Registro en Scopus
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Registro en la Biblioteca Digital
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024 7 |2 scopus  |a 2-s2.0-77952892404 
024 7 |2 cas  |a Myoglobin; Peptides 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
030 |a RCMSE 
100 1 |a Yu, Z. 
245 1 0 |a Real-time reaction monitoring by probe electrospray ionization mass spectrometry 
260 |c 2010 
270 1 0 |m Hiraoka, K.; Clean Energy Research Center, University of Yamanashi, 4-3-11 Takeda, Kofu, Yamanashi 400-8511, Japan; email: hiraoka@yamanashi.ac.jp 
506 |2 openaire  |e Política editorial 
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520 3 |a Probe electrospray ionization (PESI) is a modified version of the electrospray ionization (ESI), where the capillary for sampling and spraying is replaced by a solid needle. High tolerance to salts and direct ambient sampling are major advantages of PESI compared with conventional ESI. In this study, PESI-MS was used to monitor some biological and chemical reactions in real-time, such as acid-induced protein denaturation, hydrogen/deuterium exchange (HDX) of peptides, and Schiff base formation. By using PESI-MS, time-resolved mass spectra and ion chromatograms can be obtained reproducibly. Real-time PESI-MS monitoring can give direct and detailed information on each chemical species taking part in reactions, and this is valuable for a better understanding of the whole reaction process and for the optimization of reaction parameters. PESI-MS can be considered as a potential tool for real-time reaction monitoring due to its simplicity in instrumental setup, direct sampling with minimum sample preparation and low sample consumption. © 2010 John Wiley & Sons, Ltd.  |l eng 
593 |a Clean Energy Research Center, University of Yamanashi, Kofu, Japan 
593 |a CIHIDECAR-CONICET, Departamento de Quimica Organica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, 1428 Buenos Aires, Argentina 
593 |a Plant Biophysics/Biochemistry Research Laboratory, Faculty of Agriculture, Ehime University, Matsuyama, Japan 
593 |a College of Chemistry and Biology, Shenyang Normal University, Shenyang, China 
690 1 0 |a MYOGLOBIN 
690 1 0 |a PEPTIDE 
690 1 0 |a ARTICLE 
690 1 0 |a CHEMICAL REACTION 
690 1 0 |a CHEMICAL STRUCTURE 
690 1 0 |a CHEMISTRY 
690 1 0 |a COMPUTER SYSTEM 
690 1 0 |a ELECTROSPRAY MASS SPECTROMETRY 
690 1 0 |a EVALUATION 
690 1 0 |a HUMAN 
690 1 0 |a METHODOLOGY 
690 1 0 |a PROTEIN DENATURATION 
690 1 0 |a CHEMICAL PROCESSES 
690 1 0 |a COMPUTER SYSTEMS 
690 1 0 |a HUMANS 
690 1 0 |a MOLECULAR STRUCTURE 
690 1 0 |a MYOGLOBIN 
690 1 0 |a PEPTIDES 
690 1 0 |a PROTEIN DENATURATION 
690 1 0 |a SPECTROMETRY, MASS, ELECTROSPRAY IONIZATION 
700 1 |a Chen, L.C. 
700 1 |a Erra-Balsells, R. 
700 1 |a Nonami, H. 
700 1 |a Hiraoka, K. 
773 0 |d 2010  |g v. 24  |h pp. 1507-1513  |k n. 11  |p Rapid Commun. Mass Spectrom.  |x 09514198  |t Rapid Communications in Mass Spectrometry 
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