July 1, 2007 (Vol. 27, No. 13)

Workhorse Analytical Technique Performed on Capillary Array DNA Analyzers

N-glycosylation is one of the most common posttranslational modifications encountered on biopharmaceuticals. While the modification is often critical to achieve efficient folding and secretion of the glycoprotein drug, its notorious heterogeneity can be detrimental for downstream-processing efficiency and can significantly complicate the structural characterization of the molecule.

Moreover, the type of N-glycosylation can have a tremendous impact on the pharmacokinetics of a drug, as receptors with affinity for certain carbohydrate types are present on the liver endothelium and on hepatocytes, which cause fast clearance of glycoproteins modified with their cognate carbohydrate ligands.

For example, a protein produced in nonengineered yeast will carry high-mannose type N-glycans, which will most often be recognized by the Mannose/GlcNAc receptor on the liver endothelium and on cells of the macrophage lineage, causing disappearance from the circulation in a matter of minutes. Another well-known example concerns the N-glycosylation of erythropoietin (EPO), where large multi-antennary N-glycans are necessary to avoid renal clearance of this small protein and achieve long residence time in the circulation, which is necessary for therapeutic efficacy.

Taking this concept one step further, second-generation EPO (AraNESP, Amgen(www.amgen.com) has been engineered to contain an extra N-glycosylation site, which makes the glycoprotein molecule even larger, effectively increasing the circulation time from days to weeks.

An active field in biomanufacturing research at present is the customization of the N-glycosylation pathway of expression host cells. This ranges from merely increasing the levels of sialylation in well-established hosts like CHO cells, to full-blown pathway engineering in bacteria, yeasts, insect cells, plants, and animals. Particularly in yeasts, N-glycosylation humanization campaigns have been successful so far, although matching of the exact engineering strategy to the specific protein and its fermentation regime remains necessary. In plants, the major successes so far have been in eliminating the potentially immunogenic beta-1,2-xylose and core-alpha-1,3-fucose modifications by inactivating all genes encoding the respective glycosyltransferases. This has now been achieved in the model plant A. thaliana and in Lemna.

A lot of work remains to be done, however, to achieve fully human N-glycosylation in these organisms in a robust way, and to translate the findings to crop plants.

Figure 1

Structural Profiling Tools

In all these engineering campaigns, the availability of robust, high-resolution and high-sensitivity N-glycan structural profiling tools is of paramount importance. It also is important in monitoring production process variations for their influence on product N-glycosylation and in ensuring batch-to-batch reproducibility. Moreover, a high-throughput, low-cost analytics platform that can be operated by nonspecialist technicians is a desirable feature.

In our laboratory, the workhorse analytical technique is N-glycan profiling on the Applied Biosystems(www.appliedbiosystems.com) gel-based or capillary array-based DNA sequencers.

We provide examples here on how this method has allowed N-glycan profiling to become a technique as routine as SDS-PAGE for proteins and sequencing of DNA, effectively being executed on over 10,000 samples per year on a single four-capillary instrument.

Samples of glycoproteins are worked up through an optimized multistep 96-well plate-based protocol, and the released N-glycans are labeled with the fluorophore 8-aminopyrene-1,3,6-trisulfonic acid, followed by removal of the excess label. The workflow for sample preparation is provided in Figure 1.

In a typical N-glycan engineering campaign in the yeast Pichia pastoris, a series of vectors for the inactivation of unwanted host cell genes, for the overexpression of glycosyltransferases, etc., needs to be transformed to a wild type strain, which produces maximal levels of a target biopharmaceutical under an optimized fermentation regime. Upon each transformation round, only a fraction of the selected clones will contain the transgene in a desired genomic configuration, and among these clones, there still is significant clonal variation in the efficiency of the N-glycan engineering, which is achieved. Therefore, phenotypic screening of a relatively large number of clones is warranted to identify the clone with the most complete engineering efficiency, and to minimize the heterogeneity of the N-glycosylation pattern that is finally obtained.

To perform this screening, we grew small cultures of the clones in 24 deep-well plates covered with a gas-permeable membrane and incubated in a shaking incubator.

As a first screen, we typically prepare a rather crude extract of the cell wall glycoproteins of the clones and profile the N-glycans of these yeast-endogenous glycoproteins, which are produced at high levels.

Figure 2 shows how such analysis allows the selection of those clones with the highest engineering efficiency in a rapid fashion.

If structural information on the observed N-glycans is desired, we perform exoglycosidase array sequencing, either on the total mixture if the major compounds are of interest, or on HPLC-purified minor compounds from the mixture. The integration of a normal phase ion-pairing HPLC option in our standard workflow allows for the complete analysis of complex mixtures (Figure 3).

Along similar lines, we have employed N-glycan profiling on DNA sequencers in analysis service to academic scientists and to the biopharmaceutical industry. The high sensitivity of the integrated analytical protocols is a significant advantage of the method, with 1–5 micrograms of protein being sufficient to obtain results of exoglycosidase array sequencing. This enables the implemention of N-glycan profiling at a much earlier stage of cell-line development than has been possible in the past.

Expertise was gained for the analysis of mAb N-glycosylation at an early stage of clone selection (24-well plate culture scale) for the analysis of mAbs and total glycoprotein extracts produced in plants (proteins extracted from parts of single Arabidopsis plants are sufficient), for the analysis of N-glycans derived from Western-blotted protein bands, for recombinant Factor IX secreted by muscular tissue implants, for EPO produced in the novel expression system Leishmania tarentolae, for N-glycosylation analysis of antigens derived from parasitic trematodes, and many more.

Customized contract analytical services (specializing in miniaturized comparative analysis of larger series of samples) built on this technology and performed by the developers, are available through the ProfileThoseSugars service at BCCM/LMBP (bccm.belspo.be/about/lmbp.php); contact: Kristien Neyts (kristien.neyts @dmbr.ugent.be).

Figure 2

Nico Callewaert, Ph.D., is professor of biochemistry, Ghent University, and group leader, VIB, and Steven Geysens, Ph.D., is postdoctoral fellow, Ghent University and VIB. Wouter Laroy, Ph.D., is senior scientist at Pronota. Web: www.dmbr.ugent.be.
Phone: 32 9 33 13 843. E-mail: [email protected].

Previous articleResearch Shows Expanded Role of ncRNAs
Next articleAldagen Establishes Manufacturing Facility