Materials and reagents

Biological materials

BL21(DE3) chemically competent E. coli cells (Invitrogen, One Shot, C600003)
C57BL/6J mice (The Jackson Laboratory, 000664)

Reagents

BGUS_pET-28a(+) (GenScript, SC1691, custom-made)
XylS_pET-28a(+) (GenScript, SC1691, custom-made)
IPTG (Isopropylthio-β-galactoside) (IBI Scientific, catalog number: IB02105)
Kanamycin (IBI Scientific, catalog number: IB02120)
TALON superflow metal affinity resin (Takara Bio, catalog number: 635506)
Econo-Column chromatography columns, 1.5 cm × 10 cm, glass (Bio-Rad, catalog number: 7371512)
Nuclease, Pierce Universal nuclease (Thermo Scientific, catalog number: 88701)
30 KD cutoff concentrators, Amicon Ultra centrifugal filters (Sigma-Aldrich, catalog number: UFC803024)
Coomassie stain, G-250 stain (Bio-Rad, catalog number: 1610786)
2-mercaptoethanol (VWR, catalog number: 97064-880)
Wheat germ agglutinin (WGA), agarose bound (Vector Laboratories, catalog number: AL-1023-10)
Core DG antibody (Bio-Techne, R&D systems, catalog number: AF6868)
Anti-matriglycan antibody (DSHB, catalog number: IIH6 C4)
SOC medium (Invitrogen, One Shot, catalog number: C600003)
Acrylamide, 30% Acrylamide/Bis solution, 37.5:1 (Bio-Rad, catalog number: 1610158)
Ammonium persulfate (APS) (Sigma-Aldrich, catalog number: 248614-500G)
TEMED (RPI, catalog number: T18000-0.05)
N-Acetylglucosamine (Sigma-Aldrich, catalog number: A8625)
Bacto-Agar (BD Difco, catalog number: 214010)
Bacto-Tryptone (BD Difco, catalog number: 211705)
NaCl (IBI Scientific, catalog number: IB07071)
Yeast extract (BD Difco, catalog number: 212750)
Tris (Roche, catalog number: 11814273001)
Triton X-100 (Fisher Chemicals, catalog number: BP151)
Pepstatin (EMD-Millipore, catalog number: 516481)
PMSF (Phenylmethylsulfonyl fluoride) (Sigma-Aldrich, catalog number: P7626)
Benzamidine hydrochloride hydrate (MP Biomedicals, catalog number: 195068)
Calpeptin (EMD-Millipore, catalog number: 03-34-0051)
Calpain inhibitor (Sigma-Aldrich, catalog number: A6185)
Leupeptin (Sigma-Aldrich, catalog number: EI8)
Aprotinin (Sigma-Aldrich, catalog number: A3886)
Glycine (Bio-Rad, catalog number: 1610718)
Methanol (Sigma-Aldrich, catalog number: 179337)
KCl (potassium chloride) (Fisher Chemicals, catalog number: P217)
Na₂HPO₄ (sodium dibasic monophosphate) (Fisher Chemicals, catalog number: S374)
KH₂PO₄ (potassium dihydrogen phosphate) (Sigma-Aldrich, catalog number: P5655)
CaCl₂·2H₂O (calcium chloride) (Sigma-Aldrich, catalog number: C8106)
MgCl₂·6H₂O (magnesium chloride hexahydrate) (Fisher Chemicals, catalog number: M33)
Sodium acetate (Fisher Chemicals, catalog number: BP334)
SDS (sodium dodecyl sulfate) (SERVA, catalog number: 20765)
EDTA (ethylenediaminetetraacetic acid) (PRIMA, catalog number: KCE14000)
Filtration system PES 0.45 µm (Cole-Parmer, catalog number: UX-07630-08)

Solutions

Luria-Bertani (LB) medium (see Recipes)
Luria-Bertani (LB) agar plates-Kanamycin (see Recipes)
Lysis buffer (see Recipes)
Wash buffer 1 (see Recipes)
High salt wash buffer (see Recipes)
Elution buffer (see Recipes)
Solubilization buffer (see Recipes)
WGA wash buffer (see Recipes)
WGA elution buffer (see Recipes)
10× Phosphate buffered saline (PBS) pH 7.4 (see Recipes)
Sodium acetate buffer (see Recipes)
Two (3%–15%) SDS-PAGE separating gradient gels (see Recipes)
Two stacking gels (see Recipes)
Separating gel buffer (see Recipes)
Stacking gel buffer (see Recipes)
10× Western blot transfer buffer (see Recipes)
1× Western transfer tank buffer (see Recipes)

Recipes

Luria-Bertani (LB) medium
Reagent Final concentration Quantity
Bacto-Tryptone 1% 10 g
Yeast extract 0.5% 5 g
NaCl 1% 10 g
H₂O n/a 1,000 mL
Total n/a 1,000 mL
Autoclave for 30 min
Store at room temperature

Luria-Bertani (LB) agar plates-Kanamycin

Reagent	Final concentration	Quantity
Bacto-Tryptone	1%	10 g
Yeast extract	0.5%	5 g
NaCl	1%	10 g
Agar	2%	20 g
Kanamycin	50 μg/mL	50 μL (from 50 mg/mL stock)
H₂O	n/a	1,000 mL
Total	n/a	1,000 mL
Autoclave for 30 min Note: Add Kanamycin after media has cooled down to 65–70°C. Store plates at 4 °C

Lysis buffer

Reagent	Final concentration	Quantity	Stock concentration
Tris-HCl	50 mM	2.5 mL	1 M
NaCl	100 mM	1.25 mL	4 M
Triton X-100	1%	2.5 mL	20%
Pepstatin A	0.6 μg/mL	0.03 mL	1 mg/mL
Aprotinin	0.5 μg/mL	5 μL	5 mg/mL
Leupeptin	0.5 μg/mL	5 μL	5 mg/mL
Calpain I inhibitor	5 μM	0.05 mL	5 mM
Calpeptin	5 μM	0.05 mL	5 mM
PMSF	0.1 mM	0.05 mL	0.1 M
Benzamidine	0.75 M	0.375 mL	0.1 M
Total	n/a	50 mL
Always prepare fresh

Wash buffer 1

Reagent	Final concentration	Quantity	Stock concentration
Tris-HCl	50 mM	5 mL	1 M
NaCl	100 mM	2.5 mL	4 M
Triton X-100	0.1%	0.5 mL	20%
Pepstatin A	0.6 μg/mL	0.06 mL	1 mg/mL
Aprotinin	0.5 μg/mL	0.01 mL	5 mg/mL
Leupeptin	0.5 μg/mL	0.01 mL	5 mg/mL
Calpain I inhibitor	5 μM	0.1 mL	5 mM
Calpeptin	5 μM	0.1 mL	5 mM
PMSF	0.1 mM	0.1 mL	0.1 M
Benzamidine	0.75 mM	0.750 mL	0.1 M
Total	n/a	100 mL
Always prepare fresh

High salt wash buffer

Reagent	Final concentration	Quantity	Stock concentration
Tris-HCl	50 mM	2.5 mL	1 M
NaCl	500 mM	6.25 mL	4 M
Triton X-100	0.1%	0.25 mL	20%
Pepstatin A	0.6 μg/mL	0.03 mL	1 mg/mL
Aprotinin	0.5 μg/mL	5 μL	5 mg/mL
Leupeptin	0.5 μg/mL	5 μL	5 mg/mL
Calpain I inhibitor	5 μM	0.05 mL	5 mM
Calpeptin	5 μM	0.05 mL	5 mM
PMSF	0.1 mM	0.05 mL	0.1 M
Benzamidine	0.75 mM	0.375 mL	0.1 M
Total	n/a	50 mL
Always prepare fresh

Elution buffer

Reagent	Final concentration	Quantity	Stock concentration
Tris-HCl	50 mM	2.5 mL	1 M
NaCl	100 mM	1.25 mL	4 M
Triton X-100	0.1%	0.25 mL	20%
Imidazole	300 mM	15 mL	1 M
Pepstatin A	0.6 μg/mL	0.03 mL	1 mg/mL
Aprotinin	0.5 μg/mL	5 μL	5 mg/mL
Leupeptin	0.5 μg/mL	5 μL	5 mg/mL
Calpain I inhibitor	5 μM	0.05 mL	5 mM
Calpeptin	5 μM	0.05 mL	5 mM
PMSF	0.1 mM	0.05 mL	0.1 M
Benzamidine	0.75 mM	0.375 mL	0.1 M
Total	n/a	50 mL
Always prepare fresh

Solubilization buffer

Reagent	Final concentration	Quantity	Stock concentration
Tris-HCl	50 mM	2.5 mL	1 M
NaCl	100 mM	1.25 mL	4 M
Triton X-100	1%	2.5 mL	20%
EDTA	10 mM	1 mL	0.5 M
Pepstatin A	0.6 μg/mL	0.03 mL	1 mg/mL
Aprotinin	0.5 μg/mL	5 μL	5 mg/mL
Leupeptin	0.5 μg/mL	5 μL	5 mg/mL
Calpain I inhibitor	5 μM	0.05 mL	5 mM
Calpeptin	5 μM	0.05 mL	5 mM
PMSF	0.1 mM	0.05 mL	0.1 M
Benzamidine	0.75 mM	0.375 mL	0.1 M
Total	n/a	50 mL
Always prepare fresh

WGA wash buffer

Reagent	Final concentration	Quantity	Stock concentration
Tris-HCl	50 mM	2.5 mL	1 M
NaCl	100 mM	1.25 mL	4 M
Triton X-100	0.1%	0.25 mL	20%
EDTA	10 mM	1 mL	0.5 M
Pepstatin A	0.6 μg/mL	0.03 mL	1 mg/mL
Aprotinin	0.5 μg/mL	5 μL	5 mg/mL
Leupeptin	0.5 μg/mL	5 μL	5 mg/mL
Calpain I inhibitor	5 μM	0.05 mL	5 mM
Calpeptin	5 μM	0.05 mL	5 mM
PMSF	0.1 mM	0.05 mL	0.1 M
Benzamidine	0.76 mM	0.376 mL	0.1 M
Total	n/a	50 mL
Always prepare fresh

WGA elution buffer

Reagent	Final concentration	Quantity	Stock concentration
Tris-HCl	50 mM	2.5 mL	1 M
NaCl	100 mM	1.25 mL	4 M
Triton X-100	0.1%	0.25 mL	20%
EDTA	10 mM	1 mL	0.5 M
N-acetylglucosamine	0.3 M	3.31 grams	n/a
Pepstatin A	0.6 μg/mL	0.03 mL	1 mg/mL
Aprotinin	0.5 μg/mL	5 μL	5 mg/mL
Leupeptin	0.5 μg/mL	5 μL	5 mg/mL
Calpain I inhibitor	5 μM	0.05 mL	5 mM
Calpeptin	5 μM	0.05 mL	5 mM
PMSF	0.1 mM	0.05 mL	0.1 M
Benzamidine	0.77 mM	0.377 mL	0.1 M
Total	n/a	50 mL
Always prepare fresh

10× Phosphate buffered saline (PBS)

Reagent	Final concentration	Quantity
NaCl	1.37 M	80 g
KCl	27 mM	2 g
Na₂HPO₄	100 mM	14.4 g
KH₂PO₄	18 mM	2.4 g
CaCl₂·2H₂O	10 mM	1.33 g
MgCl₂·6H₂O	5 mM	1.0 g
H₂O	n/a	1,000 mL
Adjust pH to 7.4 with HCl
Store at room temperature

Sodium acetate buffer
Reagent Final concentration Quantity
Sodium acetate 150 mM 10.2 g
Adjust pH to 5.5
H₂O n/a 500 mL
Total n/a 500 mL
Store at room temperature
Two (3%–15%) SDS-PAGE separating gradient gels
Reagent 3% 15%
Water 19.3 mL 7.3 mL
Separating gel buffer 7.5 mL 7.5 mL
Acrylamide 3 mL 15 mL
TEMED 11 μL 11 μL
10% APS 180 μL 180 μL
Prepare fresh 10% APS
Two stacking gels
Reagent Quantity
Water 13.3 mL
Stacking gel buffer 5 mL
Acrylamide 2.3 mL
TEMED 15 μL
10% APS 150 μL
Prepare fresh 10% APS
Separating gel buffer
Reagent Final concentration Quantity
Tris
Adjust pH to 8.8 with HCL
1.5 M 90 g
SDS 0.4% 2 g
H₂O n/a 500 mL
Total n/a 500 mL
Sterilize through 0.45 μm filter
Store at room temperature
Stacking gel buffer
Reagent Final concentration Quantity
Tris
Adjust pH to 6.8 with HCL
0.5 M 30 g
SDS 0.4% 2 g
H₂O n/a 500 mL
Total n/a 500 mL
Sterilize through 0.45 μm filter
Store at room temperature
10× Western blot transfer buffer
Reagent Quantity
Glycine 288 g
Tris base 60.6 g
Water 2,000 mL
Store at room temperature
1× Western transfer tank buffer
Reagent Quantity
10× transfer buffer 400 mL
100% methanol 800 mL
Water 2,800 mL
Total 4,000 mL

Laboratory supplies

Rattler plating beads, 5 mm (Zymo Research, catalog number: S1001)
Liquid scintillation vials (RPI, catalog number: 121043)
Glass homogenizer (Cole-Parmer, catalog number: EW-44468-18)
Plain plunger (Cole-Parmer, EW-44468-06)
PVDF membrane (Immobilon-FL, Millipore, catalog number: IPFL00010)
Blotting paper (Cytiva Whatman 3MM CHR, catalog number: 3030-917)
Petri dishes (Fisher Scientific, catalog number: FB0875713)
Scissors (FST, catalog number: 14090-11)
Forceps (FST, catalog number: 91150-20)
Mortar and pestle (Fisher Scientific, catalog number: S39831)

Equipment

Thermomixer (Eppendorf, catalog number: 5382000023)
Thermo Top (Eppendorf, catalog number: 5308000003)
Polytron homogenizer (Fisher Scientific, Kinematica Polytron PT 2500 E homogenizer, catalog number: 08-451-320)
Generator/probe for Polytron homogenizer (Fisher Scientific, Kinematica, catalog number: 05-400-263)
Spectrophotometer (Eppendorf Bio photometer, model: 6131)
Water bath (Fisher Scientific, Isotemp model: 205)
Incubator (VWR, New Brunswick, Innova 42, catalog number: 75875-638)
Rotator (ATR Rotamix, model: RKVSD)
Motorized overhead stirrer (Fisher Scientific, DWK Life Sciences Wheaton, catalog number: 22-244382)
SDS-PAGE gradient gel system (Hoefer SE 600 model, 18 cm × 16 cm)
Western blot transfer system (Hoefer, TE 42 model)

Procedure

Gene cloning
1. β-glucuronidase (Bgus) from Thermotoga maritima and α-xylosidase (Xyls) from Sulfolobus solfataricus were cloned into pET-28a(+) vector between NheI/XhoI sites in frame with the N-terminal 6x-His tag by GenScript (see supplemental file S1).
Cell transformation
1. Thaw BL21DE3 competent cells on ice (50 μL aliquot for each plasmid).
2. Add 20 ng of each plasmid to the competent cells (mix by swirling the pipette tip three times).
3. Incubate cells in ice for 30 min.
4. Heat shock the cells at 42 °C for 30 s.
5. Incubate on ice again for 5 min. Critical: This step is required to obtain high efficiency of transformation.
6. Add 950 μL of SOC medium (at room temperature) and incubate at 37 °C for 60 min with shaking at 350 rpm in a thermomixer.
7. For each sample, spread 50 μL from each tube onto LB agar plates with Kanamycin (use plating beads or spreader).
8. Incubate the plates at 37 °C for 16 h.
Purification of Bgus and Xyls
1. Pick a single colony from each plate and inoculate 20 mL of LB medium (with Kanamycin, 50 μg/mL). Incubate at 37 °C for 16 h with shaking at 200 rpm.
2. Use 10 mL of the overnight culture to inoculate 1 L of LB medium (with Kanamycin, 50 μg/mL). Incubate at 37 °C with shaking at 200 rpm. Keep checking the OD₆₀₀.
3. Once the OD₆₀₀ reaches 0.6, add 1 mM IPTG (1.6 mL from a 600 mM stock solution) to the culture to induce gene expression and incubate at 16 °C for 16 h with shaking at 200 rpm.
4. Centrifuge the cells at 5,000× g for 10 min at 4 °C.
5. Store the cell pellets at -80 °C until ready for the purification step. Pause point: Cell pellets can be stored long term if necessary.
6. Dissolve the cell pellets in lysis buffer (20 mL of buffer per liter of starting culture).
7. Store the cells at -80 °C overnight to allow ice crystals to form; this step aids in cell lysis.
8. Thaw the cells at room temperature for purification.
9. Add nuclease at 6.25 kU (5 μL) concentration and sonicate cells for 5 s (power 4–5) four times with 10 s intervals at 4 °C.
10. Centrifuge cells at 15,000× g for 20 min at 4 °C. Place supernatant into a new tube.
11. Place the supernatant into a 75 °C water bath for 10 min. Critical: This step is essential to enrich the thermophilic enzymes.
12. Spin cells at 15,000× g for 30 min at 4 °C. Transfer supernatant to fresh tube. This is the cell extract.
  Note: Perform steps C13–C17 in a cold room.
13. Prepare 2 TALON superflow metal affinity columns, one for each enzyme, by packing 3 mL of resin into a Econo-Column chromatography column and equilibrating with 10 mL of wash buffer 1.
14. Apply the cell extract obtained in step C12 to the column three times. Each time, incubate the column with the extract for 15–20 min on a gentle rocking platform. Save all flowthroughs.
15. Wash the column with 10 mL of wash buffer 1 three times. Save all washes.
16. Wash the column with high salt wash buffer to remove nonspecific interactions. Save the wash.
17. Elute the bound proteins with 3 mL elution buffer in five fractions.
18. Run 100 μL of each saved wash, flowthrough, and elution on an SDS-PAGE gel and visualize with Coomassie blue.
19. Combine the relevant fractions (usually 1 and 2, see Figure 1) and buffer exchange with PBS pH 7.4 using a 30 kD Amicon concentrator. Use a total dilution factor of 200 and bring the total volume down to 1 mL. Confirm pH is approximately 7.4 with strips.
20. Aliquot the combined fractions into PCR tubes (50 μL per tube) and flash freeze in liquid nitrogen. Transfer aliquots to a -80 °C freezer for long-term storage.
  
  Figure 1. Purification of Bgus and Xyls. A. Column-purified Bgus is shown here in Eluates 1 and 2 and runs at ~66 kD in a 3%–15% gradient SDS-PAGE gel stained with Coomassie blue. B. Column-purified Xyls is shown here in Eluates 1 and 2 and runs at ~80 kD in a 3%–15% gradient SDS-PAGE gel stained with Coomassie blue.
Digestion of α-Dystroglycan (α-DG)
1. Use wheat germ agglutinin (WGA) agarose to enrich α-DG from animal tissues, as follows:
  1. Harvest 1 g of skeletal muscle from C57BL/6J mice. Pour liquid nitrogen into a mortar and pestle and crush the muscle in it.
    Note: Take muscles from the legs after euthanizing mice by cervical dislocation. Briefly, remove the skin by making a small cut in the mid-dorsal or ventral region and peel it off the mouse; then, using scissors and forceps, take all muscles from the legs including quadriceps, tibialis anterior, and soleus, until bone is visible.
  2. Transfer powdered muscle into a vial and allow to warm for 3–5 min, either on ice or in a cold room.
    Note: Vial should be able to withstand cold liquid nitrogen. We use plastic liquid scintillation vials.
  3. Add 10 mL of solubilization buffer and mince the tissue in a polytron homogenizer for 15 s at speed 4. Repeat this three times.
  4. Transfer solution to a 50 mL glass homogenizer and macerate tissue by moving the plunger in and out of the solution at least 10 times.
    Note: For macerating tissue with an automated overhead stirrer (instead of doing it by hand), use speed 4.
  5. Transfer homogenized material to a 50 mL Falcon tube and incubate on a rotator for 1 h at 4 °C.
  6. Spin the material for 30 min at 20,000× g at 4 °C. Transfer supernatant to new tube.
  7. Equilibrate 500 μL of WGA beads with 5 mL of solubilization buffer. Spin down beads at 1,500× g for 5 min. Remove buffer.
  8. Combine material obtained in step D1e with the equilibrated WGA beads and incubate for 16 h on rotator at 4 °C.
  9. Spin down beads at 1,500× g for 5 min at 4 °C and save the supernatant as WGA-void fraction.
  10. Wash WGA beads with 5 mL of WGA wash buffer by incubating for 5 min on a rotator and then spinning beads at 1,000× g for 10 min at 4 °C. Repeat this wash step four times.
  11. α-DG is now on the WGA beads. Add 1 mL of WGA elution buffer to elute α-DG from 500 μL of WGA beads and incubate at 4 °C for 1 h on a rotator.
  12. Spin down beads at 1,500× g for 5 min at 4 °C. α-DG is now in the supernatant or eluate.
2. Buffer exchange 500 μL of the WGA eluate with sodium acetate (pH 5.5) using a 30 kD Amicon concentrator. Use a total dilution factor (DF) of 80 for successfully changing the pH. Critical: This step is essential for obtaining the pH (5.5) at which both enzymes work.
  Note: For buffer exchange, follow these steps:
  1. Add 1.5 mL of sodium acetate buffer to 500 μL of WGA eluate in the upper reservoir and spin at 2,000× g for 4 min at 4 °C (DF₁ = 4). Approximately 700 μL remains in the upper reservoir. Discard the solution collected in the centrifuge tube.
  2. Add 2.1 mL of sodium acetate buffer to the 700 μL solution from the previous step (DF₂ = 4). Spin at 2,000× g for 4 min at 4 °C. Approximately 500 μL remains in the upper reservoir.
  3. Add 2 mL of sodium acetate buffer to the 500 μL solution obtained in the previous step (DF₃ =5). Spin at 2,000× g for 4 min at 4 °C. The solution in the upper reservoir (~ 500 μL) is now at pH 5.5 and the total dilution factor used is 80 (DF₁ × DF₂ × DF₃ = 4 × 4 × 5 = 80)
3. Add 10 mM β-mercaptoethanol (~ 0.7 μL from 12.8 M stock) to the buffer-exchanged eluate and heat for 5 min at 99 °C. Critical: This step is essential to remove disulfide bridges and unfold the protein to make matriglycan accessible for digestion.
4. Add all protease inhibitors (at final concentrations given in the Recipes) after the solution is cooled down.
5. Thaw the 50 μL of enzyme aliquots on ice and add them to the above mixture.
6. Aliquot 100 μL as the initial timepoint (T_o) and incubate the rest of the mixture at 75 °C for 16 h with shaking at 600 rpm in a thermomixer.
  Note: Aliquots from other timepoints can also be taken (e.g., at 4, 6, and 10 h, for T₄, T₆, and T₁₀, respectively) to check the rate of progression of the digestion. However, for complete digestion of matriglycan on DG, we recommend incubating the samples for 16–23 h (Figure 2E).
  
  Figure 2. Digestion of matriglycan by Bgus and Xyls. A, B. Wheat germ agglutinin (WGA) eluate from mouse skeletal muscle digested with Bgus and Xyls at 65 °C and 75 °C. T_ON indicates overnight digestion of 16 h. The digestion products are immunoblotted with (A) core DG antibody AF6868 1:200 and (B) anti-matriglycan antibody, IIH6, 1:100. C, D. WGA eluate of mouse skeletal muscle digested with Bgus and Xyls at 75 °C overnight (T_ON, 16 h) and immunoblotted with (C) AF6868 1:200 and (D) IIH6 1:100. E. Progress of digestion over time, as monitored at 2 (T₂), 4 (T₄), 6 (T₆), and 20 h (T₂₀); immunoblotting is with antibody against matriglycan IIH6 (1:100).
SDS-PAGE and western blotting
We analyze the progression and effectiveness of digestion by running the samples in 3%–15% SDS-PAGE gradient gels and performing immunoblotting on PVDF membranes, using antibodies against matriglycan (IIH6, 1:100), against core α-DG (AF6868 1:200) (Figure 2), and/or laminin overlay and solid phase laminin binding assay (Walimbe et al., 2020).

Data analysis

Upon successful digestion, clear shifts in the molecular weights of α-DG and matriglycan are observed. We also measure changes in laminin binding by performing laminin overlay and solid phase binding analysis (Walimbe et al., 2020, Figure 5D and 5E). Blots are scanned using a Li-Cor Odyssey imaging system and fluorescence detection, and images are analyzed using the Image Studio software. A detailed description of data analysis was provided previously (Briggs et al., 2016, Supplementary figure 1).

Validation of protocol

We have routinely used this method to identify matriglycan and found it to be robust and reproducible (Okuma et al., 2023; Briggs et al., 2016; Sheikh et al., 2020; Walimbe et al., 2020). Additional data validating our method is provided in Figure 1 and Figure 2.

General notes and troubleshooting

General notes

We have found that these enzymes are most effective when freshly purified.

Troubleshooting

If the enzymes are 4–5 months old and do not seem to work, it is best to purify fresh samples.

Acknowledgments

Research reported in this publication was supported by the National Institute of Neurological Disorders and Stroke of the National Institutes of Health under Award Number P50NS053672. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. We are thankful to Dr. Christine Blaumueller of the Scientific Editing and Research Communication Core at the University of Iowa Carver College of Medicine for her critical reading of the manuscript. We also thank Briggs et al. (2016) for first demonstrating the utility of the thermophilic enzymes in digesting matriglycan. K.P.C. is an investigator of the Howard Hughes Medical Institute.

Competing interests

The authors declare that no competing interests exist.

Ethical considerations

All mice were maintained in a barrier-free, specific pathogen-free grade facility and had access to normal chow and water ad libitum. All animals were manipulated in biosafety cabinets and change stations using aseptic procedures. The mice were maintained in a climate-controlled environment at 25 °C on a 12:12 h light/dark cycle. Animal care, ethical usage, and procedures were approved and performed in accordance with the standards set forth by the National Institutes of Health and the University of Iowa Animal Care and Use Committee (IACUC).

References

Briggs, D. C., Yoshida-Moriguchi, T., Zheng, T., Venzke, D., Anderson, M. E., Strazzulli, A., Moracci, M., Yu, L., Hohenester, E., Campbell, K. P., et al. (2016). Structural basis of laminin binding to the LARGE glycans on dystroglycan. Nat. Chem. Biol. 12(10): 810–814.
Inamori, K. I., Beedle, A. M., de Bernabe, D. B., Wright, M. E. and Campbell, K. P. (2016). LARGE2-dependent glycosylation confers laminin-binding ability on proteoglycans. Glycobiology 26(12): 1284–1296.
Liu, Y., Yu, M., Shang, X., Nguyen, M. H. H., Balakrishnan, S., Sager, R. and Hu, H. (2020). Eyes shut homolog (EYS) interacts with matriglycan of O-mannosyl glycans whose deficiency results in EYS mislocalization and degeneration of photoreceptors. Sci. Rep. 10(1): e1038/s41598-020-64752-4.
Moracci, M., Ponzano, B. C., Trincone, A., Fusco, S., De Rosa, M., van der Oost, J., Sensen, C. W., Charlebois, R. L. and Rossi, M. (2000). Identification and Molecular Characterization of the First α-Xylosidase from an Archaeon. J. Biol. Chem. 275(29): 22082–22089.
Okuma, H., Hord, J. M., Chandel, I., Venzke, D., Anderson, M. E., Walimbe, A. S., Joseph, S., Gastel, Z., Hara, Y., Saito, F., et al. (2023). N-terminal domain on dystroglycan enables LARGE1 to extend matriglycan on α-dystroglycan and prevents muscular dystrophy. eLife 12: e82811.
Praissman, J. L., Willer, T., Sheikh, M. O., Toi, A., Chitayat, D., Lin, Y. Y., Lee, H., Stalnaker, S. H., Wang, S., Prabhakar, P. K., et al. (2016). The functional O-mannose glycan on α-dystroglycan contains a phospho-ribitol primed for matriglycan addition. eLife 5: e14473.
Salleh, H. M., Müllegger, J., Reid, S. P., Chan, W. Y., Hwang, J., Warren, R. A. J. and Withers, S. G. (2006). Cloning and characterization of Thermotoga maritima β-glucuronidase. Carbohydr. Res. 341(1): 49–59.
Sheikh, M. O., Venzke, D., Anderson, M. E., Yoshida-Moriguchi, T., Glushka, J. N., Nairn, A. V., Galizzi, M., Moremen, K. W., Campbell, K. P., Wells, L., et al. (2020). HNK-1 sulfotransferase modulates α-dystroglycan glycosylation by 3-O-sulfation of glucuronic acid on matriglycan. Glycobiology 30(10): 817–829.
Walimbe, A. S., Okuma, H., Joseph, S., Yang, T., Yonekawa, T., Hord, J. M., Venzke, D., Anderson, M. E., Torelli, S., Manzur, A., et al. (2020). POMK regulates dystroglycan function via LARGE1-mediated elongation of matriglycan. eLife 9: e61388.
Yoshida-Moriguchi, T. and Campbell, K. P. (2015). Matriglycan: a novel polysaccharide that links dystroglycan to the basement membrane. Glycobiology 25(7): 702–713.
Yoshida-Moriguchi, T., Willer, T., Anderson, M. E., Venzke, D., Whyte, T., Muntoni, F., Lee, H., Nelson, S. F., Yu, L., Campbell, K. P., et al. (2013). SGK196 Is a Glycosylation-Specific O-Mannose Kinase Required for Dystroglycan Function. Science 341(6148): 896–899.

Supplementary information

The following supporting information can be downloaded here:

File S1.