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A robust micro‐electrospray ionization technique for high‐throughput liquid chromatography/mass spectrometry proteomics using a sanded metal needle as an emitter
Author(s) -
Guzzetta Andrew W.,
Thakur Rohan A.,
Mylchreest Iain C.
Publication year - 2002
Publication title -
rapid communications in mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.528
H-Index - 136
eISSN - 1097-0231
pISSN - 0951-4198
DOI - 10.1002/rcm.829
Subject(s) - chemistry , chromatography , mass spectrometry , electrospray , electrospray ionization , analytical chemistry (journal) , tandem mass spectrometry , liquid chromatography–mass spectrometry
A 60 µm internal diameter (i.d.) stainless‐steel needle was adapted to the orthogonal ESI probe (µESI) of a commercial ion trap mass spectrometer, and used for capillary liquid chromatography/tandem mass spectrometry (LC/MS/MS) protein identification experiments. The modification allows for the use of nitrogen sheath gas which helps in the nebulization at LC flow rates exceeding 500 nL/min and eliminates problems caused by liquid junctions commonly used to initiate nanospray ionization (NSI). A comparison is made between the performance of a 75 µm i.d. column with a 15 µm pulled glass tip using a liquid junction, and that of a 150 µm i.d. column using the new µESI device. The combination of the 150 µm i.d. column and µESI gave sensitivity close to that of NSI (250 attomoles horse heart myoglobin digest on column), and proved to be more robust than the standard pulled glass tips of similar i.d. No evidence of metal needle catalyzed oxidation of methionine was observed during analysis of the tetrapeptide MRFA under a range of test conditions. Phosphorylated peptides in a β‐casein tryptic digest were also successfully identified using the µESI interface with a steel needle. In addition it was found that a mild sanding of the metal needle tip improved spray performance. Copyright © 2002 John Wiley & Sons, Ltd.