Glycan Profiling of Plant Cell Wall Polymers using Microarrays

Podsumowanie

A technique called Comprehensive Microarray Polymer Profiling (CoMPP) for the characterisation of plant cell wall glycans is described. This method combines the specificity of monoclonal antibodies directed to defined glycan-epitopes with a miniature microarray analytical platform allowing screening of glycan occurrence in a broad range of biological contexts.

Streszczenie

Plant cell walls are complex matrixes of heterogeneous glycans which play an important role in the physiology and development of plants and provide the raw materials for human societies (e.g. wood, paper, textile and biofuel industries)^1,2. However, understanding the biosynthesis and function of these components remains challenging.

Cell wall glycans are chemically and conformationally diverse due to the complexity of their building blocks, the glycosyl residues. These form linkages at multiple positions and differ in ring structure, isomeric or anomeric configuration, and in addition, are substituted with an array of non-sugar residues. Glycan composition varies in different cell and/or tissue types or even sub-domains of a single cell wall³. Furthermore, their composition is also modified during development¹, or in response to environmental cues⁴.

In excess of 2,000 genes have Plant cell walls are complex matrixes of heterogeneous glycans been predicted to be involved in cell wall glycan biosynthesis and modification in Arabidopsis⁵. However, relatively few of the biosynthetic genes have been functionally characterized ^4,5. Reverse genetics approaches are difficult because the genes are often differentially expressed, often at low levels, between cell types⁶. Also, mutant studies are often hindered by gene redundancy or compensatory mechanisms to ensure appropriate cell wall function is maintained⁷. Thus novel approaches are needed to rapidly characterise the diverse range of glycan structures and to facilitate functional genomics approaches to understanding cell wall biosynthesis and modification.

Monoclonal antibodies (mAbs)^8,9 have emerged as an important tool for determining glycan structure and distribution in plants. These recognise distinct epitopes present within major classes of plant cell wall glycans, including pectins, xyloglucans, xylans, mannans, glucans and arabinogalactans. Recently their use has been extended to large-scale screening experiments to determine the relative abundance of glycans in a broad range of plant and tissue types simultaneously^9,10,11.

Here we present a microarray-based glycan screening method called Comprehensive Microarray Polymer Profiling (CoMPP) (Figures 1 & 2)^10,11 that enables multiple samples (100 sec) to be screened using a miniaturised microarray platform with reduced reagent and sample volumes. The spot signals on the microarray can be formally quantified to give semi-quantitative data about glycan epitope occurrence. This approach is well suited to tracking glycan changes in complex biological systems¹² and providing a global overview of cell wall composition particularly when prior knowledge of this is unavailable.

Protokół

1. Tissue Collection & Preparation

1. Collect 100 mg fresh weight of plant tissues (a minimum of 10 mg dry weight) in at least triplicate for each tissue of interest. The following steps describe the preparation of cell wall material from vegetative tissues. In the case of storage tissues, un-wanted starch is enzymatically removed before proceeding with the extraction of cell wall polymers as previously described¹³.
2. Homogenize the samples to a fine powder with liquid nitrogen using a Qiagen TissueLyser II, with 24 tube adapter sets and 3 mm tungsten carbide beads (30 Hz, 2 x 30 sec). Alternatively if only a few samples are being processed, a mortar and pestle is used.
3. Transfer the homogenates into 10 ml plastic conical tubes.
4. Prepare cell wall material by washing the homogenates in 10 ml 80% v/v ethanol at RT and vortexing vigorously for 2 min.
5. Centrifuge samples at 3,500 x g and discard supernatant. Repeat the 70% ethanol washes at least three times or until the supernatant is clear, particularly for tissues containing chlorophyll.
6. Perform a final wash with 100% acetone and leave the pellets containing Alcohol Insoluble Residues (AIR) to air-dry overnight.
7. Sieve the AIR samples with a 0.4 mm² mesh to achieve a fine, homogenous powder and to remove larger, poorly ground particles which sometime remain in the homogenate.
8. Weigh 10 mg AIR sample into microtubes, each containing a 3 mm glass bead to aid the mixing of samples.

2. Extraction of Cell Wall Glycans

1. Pectins, and polymers associated with pectins are extracted from the samples by adding 500 μl of 50 μM CDTA (pH 7.5) to each sample.
2. Briefly vortex the tubes to ensure the solvent is in contact with the sample material and then mix using the TissueLyser for 3 hr at 8 Hz.
3. Centrifuge samples at 12,000 x g, carefully remove the supernatants and store at 4 °C.
4. Wash pellets in 1 ml of de-ionized water to dilute and remove any remaining solvent, vortex and centrifuge at 13,000 x g. Repeat this step without disturbing the pellet and remove all liquid from the tubes before proceeding to the next step.
5. Cross-linking glycans are sequentially extracted from the remaining cell wall pellet with 500 μl of 4M NaOH with 0.1% w/v NaBH4, using the same procedure described in steps 2.1 - 2.4 for the CDTA extraction. NaBH₄ is added to reduce the aldehyde (or keto) group at the reducing end of the polysaccharides to an alcohol thereby preventing base peeling of polysaccharides.
6. After centrifugation, supernatants are again removed, stored at 4 °C, and the pellets washed twice in de-ionized water before proceeding to the next extraction.
7. As an optional step, residual polymers, such as cellulose are extracted with 500 μl cadoxen (31% v/v 1,2-diaminoethane with 0.78 M CdO) using the same procedure as described in steps 2.1 - 2.4. Alternatively, absolute cellulosic content in remaining pellets can be determined using Acetic/Nitric assays (See Discussion).

3. Printing Microarrays

1. Centrifuge supernatants containing extracted cell wall polymers at 13,000 x g to remove any particulate matter.
2. Load 50 μl of each sample into a polypropylene 384 well microtiter plate using a pre-designed custom layout where samples are arranged according to tissue type and extraction type.
3. Dilute the cell wall polymer sample in a 0, 5 and 25× serial dilution series with deionized water.
4. Parameters such as pin height, collection and dwell time, and washing steps are set on the software controlling the microarrayer.
5. The humidity of the printing chamber is controlled at 60% to prevent sample evaporation.
6. The printing job is started using LabNEXT software and a program which corresponds to the microarray layout.
7. The robot uses capillary channel pins to print solutions from the sample plate onto 20 x 20 cm nitrocellulose membrane which is attached to a flat plate in the machine. Each spot on the array contains 15 nl of solution and is printed in triplicate.
8. Identical microarrays are printed next to each other on the membrane and cut into individual arrays after the print job is complete.
9. In each experiment the arrays can be modified in order to accommodate more or less samples, dilutions or replicates.

4. Probing of Glycan Microarrays

1. After printing, block the individual microarrays in 5% w/v skimmed milk powder dissolved in phosphate buffered saline (MPBS) at room temperature for 2 hr to reduce non-specific binding.
2. Probe microarrays with monoclonal antibodies specific for cell-wall glycan epitopes for 2 hr in MPBS. The majority of monoclonal antibodies against cell wall glycans are commercially available from three companies; Biosupplies (www.biosupplies.com.au), Carbosource Services (www.carbosource.net) and PlantProbes (www.plantprobes.net).
3. Include a negative control, a microarray incubated with only MPBS and no primary antibody.
4. Wash the microarrays 3 times in phosphate buffered saline (PBS) for 5 min to remove non-specific binding.
5. Probe the microarrays with secondary antibody conjugated to horseradish peroxidase (HRP) in MPBS for 2 hr. Most monoclonal antibodies against cell wall glycans require anti-mouse or anti-rat secondary antibodies.
6. Repeat the washing steps 3 times with PBS buffer for 5 min to remove non-specific binding.
7. Develop the microarrays using chromogenic (3,3-Diaminobenzidine) or chemiluminecent (luminol) substrates.

5. Quantification

1. After development, scan the individual microarrays using a high-resolution (1,200 dpi) desktop scanner and save the images as negative, 16-bit TIFF files (Figure 3).
2. Calculate the integral intensity of each spot using Xplore Image Processing Software (LabNEXT) fitted with an automated grid tool. The integral spot intensity is derived from the sum of pixels in the grid area surrounding each spot.
3. The grid data for each microarray is exported as a txt file and can be manually imported into an Excel spreadsheet for analysis. An online tool (http://microarray.plantcell.unimelb.edu.au/ ) has been developed to automatically translate and process data from individual txt files.
4. The integral spot intensity is averaged across printing replicates and dilutions to obtain a 'mean spot intensity' value for each sample (Figure 2). Alternatively, spot signals corresponding to just one dilution value on the array are used to quantify the relative glycan epitope abundance for each sample.
5. The relative mean spot intensities between different samples are presented as a heatmap (Figure 4) using conditional formatting in excel or online heatmapper tools (http://bar.utoronto.ca/welcome.htm). The data for each antibody type is corrected to 100 and a 5% cutoff value is imposed to remove background signal and false positives.

Wyniki

The relative abundance of glycans in six tissue types (anther filaments, pollen, ovaries, petals, sepals and stigma) from Nicotiana alata flowers was determined using CoMPP. Figure 3A shows a representative microarray that has been probed with mAb JIM5 specific for partially (low) methylesterified homogalacturonan (HG), an epitope which occurs on pectic polysaccharides¹⁴. The JIM5 epitope is detected in CDTA extracts of all flower tissues however is highest in pollen and lowest in stigmatic tissue (

Dyskusje

CoMPP is a fast and sensitive method for profiling the glycan composition of hundreds plant-derived samples in a matter of days. This method complements the already available bacterial or mammalian glycan array platforms for high-throughput screening of carbohydrate interactions with glycan-binding proteins such as lectins, receptors, and antibodies¹⁶. With a large diversity of probes available for detecting cell wall glycans, it is possible to gain detailed information about glycan epitopes belonging to all m...

Materiały

Name	Company	Catalog Number	Comments
3 mm Tungsten Carbide beads	Qiagen	69997
Collection microtubes (1.2 mm)	Qiagen	19560	1.5 ml microfuge tubes can also be used
Qiagen TissueLyser II	Qiagen	85300
3 mm glass beads	Sigma Aldrich	Z143928
CDTA	Sigma Aldrich	34588
Cadmium oxide	Sigma Aldrich	202894
1,2-diamin–thane	Sigma Aldrich	03550
Nitrocellulose membrane (0.22 μm pore size)	GE-water process technologies	EP2HY00010	different pore sized membranes are suitable for different pin types
Xact II microarrayer robot	Labnext	001A	the Xact II robot was fitted with a custom 20 x 20 cm ceramic plate to which the nitrocellulose membrane is attached
Xtend RM microarray pins	Labnext	0037-350	pins must be suitable for spotting on membranes
384 well microtiter plates (polypropylene)	Greiner	781207
Anti-glycan monoclonal antibodies	Plant Probes/ CarboSource/Biosupplies		Websites; PlantProbes (www.plantprobes.net), Carbosource (www.carbosource.net) and Biosupplies (www.biosupplies.com.au).
Anti-Rat IgG (whole molecule) - Peroxidase antibody produced in goat.	Sigma	A9037	the type of secondary antibodies depends on the primary antibody used (e.g. raised in rat, mouse, goat etc).
SIGMAFAST 3,3'-Diaminobenzidine tablets	Sigma	D4293	the type of developing reagent depends on the secondary antibodies used and the detection method (colourmetric, or chemiluminecent).
SuperSignal West Pico Chemiluminescent Substrate	Thermoscientific	34080	see above
Xplore Image Processing Software	LabNext	008	many software types with automatic gridding tools are available to measure pixel value of microarray spots.
Plant polysaccharides	Sigma/Megazyme