Quantitation and Identification of Urine Mucopolysaccharides. George Gray MetBioNet Workshop 2008

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Transcription:

Quantitation and Identification of Urine Mucopolysaccharides George Gray MetBioNet Workshop 2008

The Big Questions What are we measuring? Where does it come from? How do we measure it?

What are we measuring?

What are Mucopolysaccharides?

Chondroitin Sulphate Dermatan Sulphate Heparan Sulphate Keratan Sulphate Hyaluronin GlcUA-GalNAc GalNAc GlcUA/IdUA-GalNAc GalNAc GlcUA/IdUA-GlcNAc GlcNAc Gal-GlcNAc GlcNAc GlcUA-GlcNAc GlcNAc All highly sulphated at 2,4 or 6 positions 25-10000 Polymer Units per chain

Biosynthesis Protein cores made on the ER and transferred to the cell membrane. Sequential addition of the carbohydrate units. Completed chain expelled into matrix or integrated into the cell membrane.

Catabolism Matrix MPS in endocytosed by cells and transferred to the lysosome for breakdown Peptidases break down the core protein Exoglycosidases sequentially remove the carbohydrate chain (Sulphatases and Glycosidases) Endoglycosidases (hyaluronidase, heparanidase) can partially degrade bigger molecules.

Where does it come from?

GAG Localization Comments Hyaluronin Chondroitin Sulphate Heparan Sulphate Heparin Dermatan Sulphate Keratan Sulphate Synovial fluid, Vitreous Humour, ECM of loose connective tissue Cartilage, Bone, Heart Valves Basement membranes, Components of cell surfaces Component of intracellular granules of mast cells Lining the arteries of the lungs, liver and skin Skin, Blood Vessels, Heart Valves Cornea, Bone, Cartilage aggregated with chondroitin sulphates Large polymers, shock absorbing Most abundant GAG Contains higher acetylated glucosamine than heparin More sulphated than heparan sulphates

Sources of Glycosaminoglycans How does it get in the urine? Cell Death Urine Leakage From Cells Plasma Extracellular Matrix

What sort of Glycosaminoglycans are in Urine? Molecular weights are lower than in tissues and those in patients with MPS disorders are even lower. Most glycosaminoglycans are probably partially degraded glycosaminoglycans with the core protein removed. Wide spread of molecular weights particularly in MPS patients.

How do we measure them?

Spot Tests Toluidine Blue Spot Test Alcian Blue Spot Test Albumin Turbidimetric Spot Test Cetylpyridinium Chloride Precipitation Test

Quantitative Tests Uronic Acid Quantitation Measures Glucuronic & Iduronic Acid using nasty chemicals! Does not measure keratan sulphate. Alcian Blue Quantitation 1,9 Dimethylmethylene Blue (DMB Quantitation)

Alcian Blue

Alcian Blue Quantitation Add urine to Alcian Blue in buffer ph5.8 + 10mmol/l MgCl 2 Allow to stand to precipitate GAG Wash in ethanol Resuspend pellet in solvent which release GAG. Measure OD at 690nm with appropriate standard(s) ) calculate relative to standard. Take ratio to creatinine

1,9 Dimethylmethylene Blue (DMB)

DMB Quantitation Incubate urine sample with DMB in Tris-Formate Buffer ph? Measure end point OD at 510nm with appropriate standards and relate to standard curve. Take ratio to creatinine One step assay Can be adapted for Centrifugal Analyser Requires only 60ul urine

GAG concentrations vary with age GAG mg/mmol creatinine 90 80 70 60 50 40 30 20 10 0 0 5 10 15 20 25 30 35 40 45 50 55 60 65 70 75 80 85 90 Age years

DMB Quantitation - MPS Patients GAG mg/mmol creatinine 300 290 280 270 260 250 240 230 220 210 200 190 180 170 160 150 140 130 120 110 100 90 80 70 60 50 40 30 20 10 0 0 2 4 6 8 10 12 14 16 18 20 22 24 26 28 30 32 34 36 38 40 42 44 46 48 50 52 54 56 Action Limit Age years MPS1 MPS2 MPS3 MPS4 MPS6 MPS7

Separation Techniques Thin Layer Chromatography Cellulose Acetate Electrophoresis I Dimensional 2 Dimensional

Thin Layer Chromatography GAGs are extracted from 25 ml urine by CPC or Alcian Blue precipitation with washes An aliquot of the redissolved GAG is spotted on to the plate and put through a series of six solvents of increasing ethanol concentrations containing calcium acetate. It is the stained with Alcian Blue and destained in acetic acid solution.

Cellulose Acetate Electrophoresis GAG Isolation GAGs are isolated from 2 ml urine by precipitation with Alcian Blue in 10 mmol/l MgCl 2 Redissolve in NaCl/methanol mixture and add sodium carbonate solution to facilitate precipitation on non-gag material. Centrifuge and precipitate the GAGs from the supernatant with ethanol. Resuspend the pellet in water

Cellulose Acetate Electrophoresis 1 D Electrophoresis Apply a small aliquot of dissolved isolated GAG (? fixed amount of GAG) on to a rectangular membrane (? 8 samples including standards and a Morquio QA). Subject to electrophoresis in a barium acetate buffer ph 5.8 for 4-54 5 hours. Stain with Alcian Blue and destain in acetic acid solution.

Cellulose Acetate Electrophoresis 2 D Electrophoresis Apply 1-2ul 1 of GAG solution to the corner of a square membrane. Subject to electrophoresis in pyridine:acetic acid:water 1-1.51.5 hours. Turn through 90 degrees and subject to electrophoresis for 3 hours in barium acetate buffer. Stain in Alcian Blue and destain in acetic acid.

One Dimensional Cellulose Acetate Electrophoresis

Two Dimensional Electrophoresis

Two Dimensional Electrophoresis MPS2

Two Dimensional Electrophoresis Electrophoresis MPS4

Anomalies If large loads are used traces of dermatan and keratan sulphate are occasionally seen. Hyaluronic Acid may very occasionally appear as a narrow band between Chondroitin and Heparan Sulphate. It has been reported to be excreted in certain renal tumours and is regularly seen in amniotic fluid.

Problems Infected urines rarely a problem. Infection level needs to be high to cause problems. Slys (MPS VII) can be difficult! Heparin be wary of apparently raised heparan sulphate in samples from patients on ITU or cardiac patients. Drugs-rarely rarely a problem Funny spots and bands lubricants used on the skin may contain mucopolysaccharides. It is more common in urines collected in bags, It is said that sometimes neonates may not be clearly abnormal in some disorders Adult patients sometimes do not have as clearly abnormal patterns

Amniotic Fluid GAGs GAGs can be isolated from the amniotic fluid supernatant collected at 16-18 18 week gestation. The position and pattern of individual GAGs can vary slightly form the ones in urine. Hyaluronic Acid is a major component. The test can reliably detect MPS1 & II but MPS III & IV can sometimes be a problem It is best to do both 1D and 2D electrophoresis.

Quality Assurance Internal GAG Standards are from non-human sources! External EQA Scheme run by Willink Unit 3 urine samples 3-43 4 times per year Reports on screening tests, quantitation and separation technique results. -ERNDIM analyte scheme GAG Quantitation only