Deficiency in human lysosomal α-mannosidase (MAN2B1) results in α-mannosidosis, a lysosomal storage disorder; patients present a wide range of neurological, immunological, and skeletal symptoms caused by a multisystemic accumulation of mannose-containing oligosaccharides. Here, we describe the expression of recombinant MAN2B1 both transiently in Nicotiana benthamiana leaves and in the leaves and seeds of stably transformed N. tabacum plants. After purification from tobacco leaves, the recombinant enzyme was found to be N-glycosylated and localized in vacuolar compartments. In the fresh leaves of tobacco transformants, MAN2B1 was measured at 10,200 units/kg, and the purified enzyme from these leaves had a specific activity of 32-45 U/mg. Fur...
Neutral alpha-mannosidase and lysosomal MAN2B1 alpha-mannosidase belong to glycoside hydrolase famil...
Plant-specific N-glycosylation can represent an important limitation for the use of recombinant glyc...
Kifunensine, a potent and selective inhibitor of class I α-mannosidases, prevents α-mannosidases I f...
Deficiency in human lysosomal α-mannosidase (MAN2B1) results in α-mannosidosis, a lysosomal storage ...
The transport of secretory proteins from the endoplasmic reticulum to the vacuole requires sorting s...
Mucopolysaccharidosis (MPS) I is a lysosomal storage disease caused by a deficiency of α-L-iduronida...
Genetic deficiency of acid alpha glucosidase (GAA) results in glycogen storage disease type II (GSDI...
A mannose selection system was evaluated for its potential application as a selectable marker in tob...
Lysosomal alpha-mannosidase (EC 3.2.1.24) is required in the degradation of the asparagine-linked ca...
There is a clear need for efficient methods to produce protein therapeutics requiring mannose-termin...
β-mannosidase (EC 3.2.1.25, MANB) dissects the non-reducing end of N-linked mannose moie-ties of gly...
Gaucher disease is caused by a deficiency of the enzyme glucocerebrosidase (GCase). Currently, enzym...
In recent years, plants have been developed as an alternative expression system to mammalian hosts f...
α-Galactosidases (EC 3.2.1.22) are retaining glycosidases that cleave terminal α-linked galactose re...
Kifunensine, a potent and selective inhibitor of class I α-mannosidases, prevents α-mannosidases I f...
Neutral alpha-mannosidase and lysosomal MAN2B1 alpha-mannosidase belong to glycoside hydrolase famil...
Plant-specific N-glycosylation can represent an important limitation for the use of recombinant glyc...
Kifunensine, a potent and selective inhibitor of class I α-mannosidases, prevents α-mannosidases I f...
Deficiency in human lysosomal α-mannosidase (MAN2B1) results in α-mannosidosis, a lysosomal storage ...
The transport of secretory proteins from the endoplasmic reticulum to the vacuole requires sorting s...
Mucopolysaccharidosis (MPS) I is a lysosomal storage disease caused by a deficiency of α-L-iduronida...
Genetic deficiency of acid alpha glucosidase (GAA) results in glycogen storage disease type II (GSDI...
A mannose selection system was evaluated for its potential application as a selectable marker in tob...
Lysosomal alpha-mannosidase (EC 3.2.1.24) is required in the degradation of the asparagine-linked ca...
There is a clear need for efficient methods to produce protein therapeutics requiring mannose-termin...
β-mannosidase (EC 3.2.1.25, MANB) dissects the non-reducing end of N-linked mannose moie-ties of gly...
Gaucher disease is caused by a deficiency of the enzyme glucocerebrosidase (GCase). Currently, enzym...
In recent years, plants have been developed as an alternative expression system to mammalian hosts f...
α-Galactosidases (EC 3.2.1.22) are retaining glycosidases that cleave terminal α-linked galactose re...
Kifunensine, a potent and selective inhibitor of class I α-mannosidases, prevents α-mannosidases I f...
Neutral alpha-mannosidase and lysosomal MAN2B1 alpha-mannosidase belong to glycoside hydrolase famil...
Plant-specific N-glycosylation can represent an important limitation for the use of recombinant glyc...
Kifunensine, a potent and selective inhibitor of class I α-mannosidases, prevents α-mannosidases I f...