Application of combined high-performance thin-layer chromatography immunostaining and nanoelectrospray ionization quadrupole time-of-flight tandem mass spectrometry to the structural characterization of high- and low-affinity binding ligands of Shiga toxin 1

• Published in: Rapid communications in mass spectrometry Vol. 19; no. 24; pp. 3659 - 3665
• Main Authors: Meisen, Iris, Friedrich, Alexander W., Karch, Helge, Witting, Ute, Peter-Katalinić, Jasna, Müthing, Johannes
• Format: Journal Article
• Language: English
• Published: Chichester, UK John Wiley & Sons, Ltd 30.12.2005
• Subjects: Antibodies - immunology; Chromatography, Thin Layer - methods; Globosides - analysis; Globosides - chemistry; Globosides - immunology; Immunoassay - methods; Ligands; Protein Binding; Shiga Toxin 1 - metabolism; Silica Gel; Silicon Dioxide; Spectrometry, Mass, Electrospray Ionization - methods; Trihexosylceramides - analysis; Trihexosylceramides - chemistry; Trihexosylceramides - immunology
• ISSN: 0951-4198; 1097-0231
• DOI: 10.1002/rcm.2241

Shiga toxin 1 (Stx1) represents an AB5 toxin produced by enterohemorrhagic Escherichia coli, which cause gastrointestinal diseases in humans that are often followed by potentially fatal systemic complications, such as acute encephalopathy and hemolytic uremic syndrome. The expression of the preferential Stx1 receptor, Gb3Cer/CD77 (Galα1‐4Galβ1‐4Glcβ1‐1Cer), is one of the primary determinants of susceptibility to tissue injury. Due to the clinical importance of this life‐threatening toxin, a combined strategy of preparative high‐performance thin‐layer chromatography (HPTLC) overlay assay and mass spectrometry was developed for the detection and structural characterization of Stx1‐binding glycosphingolipids (GSLs). A preparation of neutral GSLs from human erythrocytes, comprising 21.4% and 59.1% of the high‐ and low‐affinity Stx1‐binding ligands Gb3Cer/CD77 and Gb4Cer, respectively, was separated on silica gel precoated HPTLC plates and probed for the presence of Stx1 receptors. Stx1 positive on the one hand and anti‐Gb3Cer/CD77 and anti‐Gb4Cer antibody positive bands from parallel reference runs on the other hand were extracted with chloroform/methanol/water (30/60/8, v/v/v). These crude extracts were used without any further purification for a detailed structural analysis by nanoelectrospray ionization quadrupole time‐of‐flight mass spectrometry (nanoESI‐QTOF‐MS) in the negative ion mode. In all extracts investigated, neutral GSLs were detected as singly charged deprotonated molecular ions, [M–H]−, and neither buffer‐derived salt adducts nor coextracted contaminants from the overlay assay procedure or the silica gel layer were observed. For the structural characterization of Stx1‐ and antibody‐binding GSLs low‐energy collision‐induced dissociation (CID) was applied to high and low abundant receptor species of the crude extracts. All MS/MS spectra obtained contained full series of Y‐type ions, B‐type ions and additional ions generated by ring cleavages of the sugar moiety. Only analytical quantities in the microgram scale of a single GSL species within the complex GSL mixture were required for the structural MS characterization of Stx1 ligands as Gb3Cer/CD77 and Gb4Cer. This effective combined HPTLC/MS procedure offers a broad range of applications, not only for toxins of bacterial origin, but also for any GSL‐binding agents such as plant‐derived lectins or human proteins with yet unknown binding specificities. Copyright © 2005 John Wiley & Sons, Ltd.