PREISLER, Jan, Ping HU, Barry, L. KARGER, Tomáš REJTAR a Eugene MOSKOVEETS. Capillary Array Electrophoresis-MALDI Mass Spectrometry Using a Vacuum Deposition Interface. Analytical Chemistry. Washington, D.C., USA: American Chemical Society, 2002, roč. 74, č. 1, s. 17-25. ISSN 0003-2700.
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Základní údaje
Originální název Capillary Array Electrophoresis-MALDI Mass Spectrometry Using a Vacuum Deposition Interface
Autoři PREISLER, Jan (203 Česká republika, garant), Ping HU (156 Čína), Barry, L. KARGER (840 Spojené státy), Tomáš REJTAR (203 Česká republika) a Eugene MOSKOVEETS (643 Rusko).
Vydání Analytical Chemistry, Washington, D.C., USA, American Chemical Society, 2002, 0003-2700.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 10406 Analytical chemistry
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
Impakt faktor Impact factor: 5.094
Kód RIV RIV/00216224:14310/02:00008542
Organizační jednotka Přírodovědecká fakulta
UT WoS 000173086200010
Klíčová slova anglicky capillary array electrophoresis; MALDI; mass spectrometry; proteomics; peptide
Štítky capillary array electrophoresis, MALDI, mass spectrometry, peptide, proteomics
Změnil Změnil: prof. Mgr. Jan Preisler, Ph.D., učo 45329. Změněno: 28. 6. 2009 00:01.
Anotace
The approach of vacuum deposition has been extended to demonstrate parallel analysis for multiple on-line infusion MALDI TOF MS and capillary array electrophoresis (CAE)-MALDI MS. In the infusion mode, individual peptide samples were simultaneously deposited on a Mylar tape cartridge using an array of eight capillaries, yielding eight parallel traces. For CAE-MALDI/TOF MS, the same number of separation capillaries were coupled with an array of eight infusion capillaries using a common liquid junction, containing matrix solution. A fast-scanning mirror was employed to traverse the beam of the desorption laser across the Mylar tape to probe one trace at a time. The positions of the eight sample traces formed on the tape were automatically determined, and all samples were analyzed in rapid sequence using a kilohertz repetition rate laser and a high-throughput data acquisition system. The instrumentation was operated with CAE MS for high-throughput analysis without compromising data quality applicable to MALDI/TOF MS analysis for proteomics and other areas where separation and high throughput are required.
VytisknoutZobrazeno: 5. 5. 2024 20:53