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On‐line sample clean‐up and chromatography coupled with electrospray ionization mass spectrometry to characterize the primary sequence and disulfide bond content of recombinant calcium binding proteins
Author(s) -
Johnson Kenneth L.,
Veenstra Timothy D.,
Londowski James M.,
Tomlinson Andy J.,
Kumar Rajiv,
Naylor Stephen
Publication year - 1999
Publication title -
biomedical chromatography
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.4
H-Index - 65
eISSN - 1099-0801
pISSN - 0269-3879
DOI - 10.1002/(sici)1099-0801(199902)13:1<37::aid-bmc810>3.0.co;2-p
Subject(s) - chemistry , electrospray ionization , chromatography , mass spectrometry , cysteine , recombinant dna , electrospray , molecular mass , biochemistry , enzyme , gene
We have used on‐line sample clean‐up, concentration, and chromatography with electrospray ionization mass spectrometry (ESI–MS), to characterize and determine the presence of disulfide bonds in recombinant full‐length rat brain calbindin D 28K and two deletion mutants of the protein, one lacking EF‐hand 2 (calbindin Δ2) and the other lacking EF‐hands 2 and 6 (calbindin Δ2,6). The molecular weights of the expressed proteins dissolved in biological buffers were determined with high accuracy using a low‐flow, pressurized chamber infusion system, that allows on‐line protein clean‐up by removing buffers/salts incompatible with ESI–MS. The molecular weight determinations showed that the amino‐terminal methionine residues had been cleaved during the expression and isolation of the recombinant proteins. Approximately 85–90% of the protein sequences were confirmed by on‐line HPLC–ESI–MS analysis of peptides generated by a lysyl endoproteinase C digestion. Comparisons of ESI–MS spectra of native and reduced calbindin D 28K and Δ2 show that the full length‐ and Δ2 mutant‐protein contain one disulfide bond. Molecular mass determinations of calbindin Δ2,6 showed that this protein contains a highly active cysteine residue that covalently binds a mercaptoethanol group, or forms a homodimer via a disulfide bond. The results show surprising differences amongst the deletion mutants of calbindin D 28K with respect to the formation of disulfide bonds. These differences are not readily detected by other techniques and show that ESI–MS is a powerful, rapid method by which to detect disulfide linkages for intact proteins. Copyright © 1999 John Wiley & Sons, Ltd.