Ashok K. Shukla

Hydrophilic-interaction chromatography of complex carbohydrates

Complex carbohydrates can frequently be separated using hydrophilic-interaction chromatography (HILIC). The mechanism was investigated using small oligosaccharides and a new column, PolyGLYCOPLEX. Some carbohydrates exhibited anomer separation, which made it possible to determine the orientation of the reducing end relative to the stationary phase. Amide sugars were consistently good contact regions. Relative to amide sugars, sialic acids and neutral hexoses were better contact regions at lower levels of organic solvents than at higher levels. HILIC readily resolved carbohydrates differing in residue composition and position of linkage. Complex carbohydrate mixtures could be resolved using volatile mobile phases. This was evaluated with native glycans and with glycans derivatized with 2-aminopyridine or a nitrobenzene derivative. Both asialo- and sialylated glycans could be resolved using the same set of conditions. With derivatized carbohydrates, detection was possible at the picomole level by UV detection or on-line electrospray mass spectrometry. Selectivity compared favorably with that of other modes of HPLC. HILIC is promising for a variety of analytical and preparative applications.

The anti-recognition function of sialic acids: studies with erythrocytes and macrophages

Sialic acids have been found to mask antigens, receptors and other recognition sites on molecules and cells. This has been investigated best with hepatocyte and macrophage lectins which recognize 13-galactose and N-acetyl-13-galactosamine residues on molecules and cells exposed by sialidase treatment. The lectin on macrophages leads to the binding and phagocytosis of erythrocytes after the enzymic removal of a critical amount of sialic acids. New techniques (colorimetry, high-performance liquid chromatography, gas-liquid chromatographymass spectrometry) for the determination of the amount and nature of these sialic acids were developed. The interaction of partially desialylated rat erythrocytes with homologous peritoneal macrophages can be inhibited by 13-galactosyl glycosides in a degree depending on the structure of the oligosaccharides and glycoconjugates tested. Although homologous serum stimulates binding and phagocytosis, immunoglobulins and complement factors were found to play no role in this process. The main factor responsible for the masking effect of sialic acids on subterminal 13-galactosyl groups seems to be the carboxyl group of neuraminic acid, as reduction of this group to an alcohol largely abolishes this important function of sialic acids in the macrophage and hepatocyte systems studied. The anti-recognition function of sialic acids illuminates the pathophysiological role of serum sialidases in infectious and other diseases.

Analysis of N,O-acylated neuraminic acids by high-performance liquid anion-exchange chromatography

Abstract Analysis of different neuraminic acid derivatives can be performed within 10 min on a small column (40 × 4.6 mm) filled with the strong basic anion-exchange resin Aminex A-28 (particle size 9 μm), using 0.75 mM sodium sulphate solution as mobile phase. (For instance, the following retention times in seconds were obtained: N-acetylneuraminic acid, 361; N-glycolylneuraminic acid, 480; N-acetyl-9-mono-O-acetylneuraminic acid, 530). The effect of other anions such as chloride and acetate on the separation is described. The method allows determination of amounts of sialic acids as small as 6 ng (20 pmol). It is also used for the separation of sialyllactose isomers, sialyllactosamine and CMP-N-acetylneuraminic acid, and is compared with the behaviour of several neutral sugars and N-acylmannosamines. The method can be applied to follow enzymatic reactions of the sialic acid metabolism such as the actions of sialidase and N-acetylneuraminate lyase, and for preparation of individual sialic acids in small quantities. If combined with colorimetry, thin-layer or gas—liquid chromatography or with specific enzyme reactions, this method represents the fastest, most sensitive and specific technique available for the analysis of sialic acids.

Analysis of sialidase and N-acetylneuraminate pyruvate-lyase substrate specificity by high-performance liquid chromatography.

A rapid and sensitive assay by high-performance liquid chromatography for determination of the activity and substrate specificity of sialidase (EC 3.2.1.18) and N-acetylneuraminate lyase (EC 4.1.3.3) is described. Sialic acids were separated on a strong anion-exchange resin using 0.75 mM sodium sulfate as elution medium. This method allows the determination of a minimum amount of 200 pg (0.6 pmol) of sialic acid. Usually the enzyme mixtures were directly applied to the column without prior purification of substrates and products. The action of sialidase was studied either by the decrease of sialyllactose concentration or by the amount of sialic acid liberated. The relative hydrolysis rates of N-acetylneuraminyl-alpha(2-3)-lactose, N-glycolylneuraminyl-alpha(2-3)-lactose, N-acetylneuraminyl-alpha(2-6)-lactose, N-acetyl-9-O-acetylneuraminyl-alpha(2-3)-lactose, and N-acetyl-4-O-acetylneuraminyl-alpha(2-3)-lactose by Vibrio cholerae sialidase were 100, 88, 25, 12, and 0, respectively. The activity of N-acetylneuraminate lyase from Clostridium perfringens was determined by measuring the rate of disappearance of sialic acids or the formation of acylmannosamines, which is possible in the same chromatogram. Relative cleavage rates of N-acetylneuraminic acid, N-glycolylneuraminic acid, N-acetyl-9-O-acetylneuraminic acid, N-acetyl-7-O-acetylneuraminic acid, and N-acetyl-4-O-acetylneuraminic acid were found to be 100, 67, 24, 3, and 0, respectively. Comparison of the substrate specificities shows that substituents on the neuraminic acid molecule influence the reactions of both enzymes in a similar way.

High-performance liquid chromatography of N,O-acylated sialic acids

Abstract A rapid, isocratic high-performance liquid chromatographic method for the analysis of N -acetylneuraminic acid, N -glycolylneuraminic acid, and their O -acetylated derivatives is described. Separation of sialic acids and of other monosaccharides as sugar-borate complexes is achieved on an anion-exchange resin. The sialic acids elute as individual peaks after the other sugars tested. The method allows quantitative determination, for example, of amounts of N -acetylneuraminic acid as small as 10 nmol. On cation-exchange resin sialic acids cannot be differentiated, but can be separated from neutral and amino sugars, allowing the determination of as little as 3 nmol of total sialic acids.

Reconstitution of the masking effect of sialic acid groups on sialidase-treated erythrocytes by the action of sialyltransferases

Glutardialdehyde-fixed or native rat erythrocytes were partially desialylated by the action of Vibrio cholerae sialidase, resulting in the binding of these cells to homologous peritoneal macrophages. Resialylation of these erythrocytes by purified alpha-(2----3)- or alpha-(2----6)-sialyltransferases with CMP-N-acetylneuraminic acid led to the incorporation of 60-80% of the enzymically released sialic acid. Binding of the resialylated erythrocytes to peritoneal macrophages was reduced when compared with corresponding, partially desialylated erythrocytes. Thus, the amount of transferred sialic acid was sufficient to demonstrate reconstitution of the masking effect of sialic acids.

Determination of 3-deoxy-d-manno-octulosonic acid (KDO), N-acetylneuraminic acid, and their derivatives by ion-exchange liquid chromatography

A liquid chromatography (1.6 MPa) system for the analysis of 3-deoxy-D-manno-2-octulosonic acid (KDO), N-acetylneuraminic acid (Neu5Ac), methyl alpha- and beta-glycosides of Neu5Ac and KDO, alpha-heptosyl-(1----5)-KDO, various sialyllactoses, alpha-KDO-(2----4)-KDO, alpha-KDO-(2----4)-KDO methyl alpha-glycoside, beta-KDO-(2----4)-KDO methyl beta-glycoside, D-glucuronic acid, D-glucurono-3,6-lactone, and D-galacturonic acid has been developed. Separation was achieved within 10 and 30 min by the use of a small column filled with a strongly basic, anion-exchange resin, Aminex A-29, and 0.75 or 10mM sodium sulfate solutions as mobile phases. This method allowed the determination of KDO and sialic acids in amounts of 100 ng (0.5 nmol) and 200 pg (0.6 pmol), respectively.

Structural analysis of underivatized sialic acids by combined high-performance liquid chromatography—mass spectrometry

Mass spectra of chemically ionized, positive ions of underivatized N,O-acylated sialic acids, 2-deoxy-2,3-didehydro-N-acetylneuraminic acid and sialyl-alpha(2-3)-lactose were obtained by combined high-performance liquid chromatography--mass spectrometry, using a direct liquid inlet system. The mass spectra of the different compounds for which fragmentation schemes are proposed enable the differentiation between sialic acids, although the localization of O-substituents is not possible. However, since the various sialic acids separated well on high-performance liquid chromatography, combined high-performance liquid chromatography-mass spectrometry allowed their unequivocal characterization.

New Techniques for the Investigation of Structure and Metabolism of Sialic Acids

Sialic acid analysis in biological material including gangliosides is often confronted with the necessity to determine trace amounts of various N,O-substituted species. Therefore, techniques of high sensitivity and resolution are required, such as capillary gas-liquid chromatography (GLC) and high performance liquid chromatography (HPLC). Both methods in combination with mass spectrometry allow structural analysis of the different neuraminic acid derivatives. Thus, the number of natural sialic acids known so far has increased to more than 30, including non only saturated, but also 2,3-unsaturated and 2,7-anhydro-sialic acids. Furthermore, HPLC has proved to be especially useful for the study of enzyme reactions, as the sialic acids of enzyme assay mixtures in most cases can be analyzed without prior extensive purification or derivatization.

Natural occurrence and preparation of O-acylated 2,3-unsaturated sialic acids

Three O-acylated, unsaturated sialic acids, N-acetyl-9-O-acetyl-, N-acetyl-9-O-lactoyl-, and 2-deoxy-N-glycoloyl-9-O-lactoyl-2,3-didehydroneuraminic acid (5-acetamido-9-O-acetyl-, 5-acetamido-9-O-lactoyl-, and 2,6-anhydro-3,5-dideoxy-5-glycoloylamido-9-O-lactoyl-D-glycero-D-g alacto-non-2- enonic acid) were isolated from urine or submandibular glands of rat, pig, and cow. Mass spectrometric evidence for the existence of 2,3-unsaturated 9-O-acetyl-N-glycoloylneuraminic acid in porcine urine was also obtained. The sialic acids were purified by dialysis, gel- and ion-exchange chromatography, and preparative thin-layer chromatography. They were analyzed by thin-layer chromatography, high-pressure liquid chromatography, and capillary gas-liquid chromatography-mass spectrometry. For comparison, O-acetylated unsaturated sialic acids were synthesized.