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PNGase F |
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- Specific Activity: 1,800,000 units/mg
- Supplied with 10X Reaction Buffer, 10X Denaturation Buffer and 10% NP-40
Description: Peptide: N-Glycosidase F, also known as PNGase F, is an amidase that cleaves between the innermost GlcNAc and asparagine residues of high mannose, hybrid, and complex oligosaccharides from N-linked glycoproteins (1)



 PNGase F hydrolyzes nearly all types of N-glycan chains from glycopeptides/proteins. [x = H or sugar(s)]


 Source: PNGase F is purified from Flavobacterium meningosepticum (2).
Applications:- Removal of carbohydrate residues from proteins
Reagents Supplied: G7 Reaction Buffer (10X)
Glycoprotein Denaturing Buffer (10X)
NP-40 (10%)
Enzyme Properties

 Molecular Weight: Apparent: 36,000 daltons
Specific Activity: 1,800,000 units/mg
Reaction & Storage Conditions

 Reaction Conditions: 1X G7 Reaction Buffer Supplemented with 1 % NP-40 Incubate at
37°C.
1X G7 Reaction Buffer: 50 mM sodium phosphate
pH 7.5 @ 25°C
Unit Definition: One unit is defined as the amount of enzyme required to remove > 95% of the carbohydrate from 10 µg of denatured RNase B in 1 hour at 37°C in a total reaction volume of 10 µl (65 NEB units = 1 IUB milliunit).
Unit Definition Assay: 10 µg of RNase B are denatured with 1X Glycoprotein Denaturing Buffer at 100°C for 10 minutes. After the addition of NP-40 and G7 Reaction Buffer, two-fold dilutions of PNGase F are added and the reaction mix is incubated for 1 hour at 37°C. Separation of reaction products are visualized by SDS-PAGE.
Concentration: 500,000 units/ml
Storage Conditions: 20 mM Tris-HCl 50 mM NaCl 5 mM EDTA 50% Glycerol
pH 7.5 @ 25°C
Storage Temperature: -20°C
Notes

 Usage notes:- Since PNGase F activity is inhibited by SDS, it is essential to have NP-40 present in the reaction mixture. Why this non-ionic detergent counteracts the SDS inhibition is unknown at present.
- To deglycosylate a native glycoprotein, longer incubation time as well as more enzyme may be required.
- PNGase F will not cleave N-linked glycans containing core α1-3 Fucose.
- Activity at different temperatures (measured after a 1 hour incubation of glycosidase and denatured RNase B at the given temperature): 37°C - 100%; 30°C - 100%; 23°C - 65%; 17°C - 40% and 3°C - 0%.
- Typical reaction conditions: Please see FAQs.
FAQs


- I tried the PNGase F on my glycoprotein and didn't see removal of the carbohydrate. What could be the problem?
- What is the difference between PNGase F and Endo H?
- How much PNGase F should I use to remove my carbohydrate under native conditions?
- How do I inhibit PNGase F?
- What is a good endoglycosidase substrate?
- Does PNGase F work in Urea?
- Do detergents inhibit exoglycosidases/endoglycosidases?
- What are the typical reaction conditions for PNGase F?
- Why is my immunoprecipitated (IP) protein degraded? When I denature and add SDS all I see on my SDS-PAGE is a smear or no protein?
- What are Glycosidases and their uses?
Quality Control for Current Lot

 Quality control values for a specific lot can be found on the datacard which accompanies each product.
Quality Assurance Statement: No contaminating exoglycosidase or Endoglycosidase F2 or F3 activity could be detected. < 0.01% of Endoglycosidase F1 could be detected. No contaminating proteolytic activity could be detected.
Glycosidase Assays: 5,000 units of PNGase F were incubated with 0.1 mM of fluorescently-labeled oligosaccharides and glycopeptides, in a 10 µl reaction for 20 hours at 37°C. The reaction products were analyzed by TLC for digestion of substrate.
No other glycosidase activities were detected (ND) with the following substrates:
β-N-Acetylglucosaminidase: GlcNAcβ1-4GlcNAcβ1-4GlcNAc-AMC ND
α-Fucosidase: Fucα1-2Galβ1-4Glc-AMCGalβ1-4(Fucα1-3)GlcNAcβ1-3Galβ1-4Glc-AMC ND
β-Galactosidase: Galβ1-3GlcNAcβ1-4Galβ1-4Glc-AMC ND
α-Galactosidase: Galα1-3Galβ1-4Galα1-3Gal-AMC ND
α-Neuraminidase: Neu5Acα2-3Galβ1-3GlcNAcβ1-3Galβ1-4Glc-AMC ND
α-Mannosidase: Manα1-3Manβ1-4GlcNAc-AMC ND Manα1-6Manα1-6(Manα1-3)Man-AMC ND
β-Glucosidase: Glcβ1-4Glcβ1-4Glc-AMC ND
β-Xylosidase: Xylβ1-4Xylβ1-4Xylβ1-4Xyl-AMC ND
β-Mannosidase: Manβ1-4Manβ1-4Man-AMC ND
Endo F1, F2, H: Dansylated invertase high mannose. ND
Endo F2, F3: Dansylated fibrinogen biantennary ND
Protease Assay: After incubation of 10,000 units of PNGase F with 0.2 nmol of a standardized mixture of proteins, for 20 hours at 37°C, no proteolytic activity could be detected by SDS-PAGE.
References


- Maley, F. et al. (1989) Anal. Biochem., 180, 195-204.
- Plummer, T.H. Jr. and Tarentino, A.L. (1991) Glycobiology, 1, 257-263.
Companion Products

 Endo H Endo Hf Endoglycosidase Reaction Buffer Pack PNGase F (Glycerol Free) RNase B
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