TY - JOUR
T1 - A microassay for acid β-galactosidase activity toward asialofetuin
AU - Mutoh, Tatsuro
AU - Naoi, Makoto
AU - Sobue, Itsuro
AU - Kiuchi, Kazutoshi
AU - Nagatsu, Toshiharu
N1 - Funding Information:
This work was supported by grants from the Ministry Culture of Japan.
PY - 1985/11/15
Y1 - 1985/11/15
N2 - To study the enzymatic properties of β-galactosidase from the patients with a β-galactosidase deficiency such as GM1 gangliosidosis, determination of enzymatic activity with naturally occurring substrates, asialofetuin in addition to another natural substrate, GM1 ganglioside, is essentially required. With a previously reported, simple and sensitive fluorometric assay for GM1 ganglioside β-galactosidase using high performance liquid chromatography (HPLC), optimal reaction conditions were determined for the assay of acid β-galactosidase activity toward asialofetuin in skin fibroblast homogenates. Under these conditions, reduced enzymatic activities could be detected in cultured skin fibroblasts from patients with type 1 and 3 GM1 gangliosidoses and mucopolysaccharidosis IV-B (Morquio B syndrome). This method was applicable to study of the enzymatic properties of the mutant β-galactosidase and provided an alternative to assays employing radioactive or artificial substrates.
AB - To study the enzymatic properties of β-galactosidase from the patients with a β-galactosidase deficiency such as GM1 gangliosidosis, determination of enzymatic activity with naturally occurring substrates, asialofetuin in addition to another natural substrate, GM1 ganglioside, is essentially required. With a previously reported, simple and sensitive fluorometric assay for GM1 ganglioside β-galactosidase using high performance liquid chromatography (HPLC), optimal reaction conditions were determined for the assay of acid β-galactosidase activity toward asialofetuin in skin fibroblast homogenates. Under these conditions, reduced enzymatic activities could be detected in cultured skin fibroblasts from patients with type 1 and 3 GM1 gangliosidoses and mucopolysaccharidosis IV-B (Morquio B syndrome). This method was applicable to study of the enzymatic properties of the mutant β-galactosidase and provided an alternative to assays employing radioactive or artificial substrates.
UR - http://www.scopus.com/inward/record.url?scp=0022377743&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0022377743&partnerID=8YFLogxK
U2 - 10.1016/0009-8981(85)90106-8
DO - 10.1016/0009-8981(85)90106-8
M3 - Article
C2 - 2415273
AN - SCOPUS:0022377743
SN - 0009-8981
VL - 152
SP - 307
EP - 314
JO - Clinica Chimica Acta
JF - Clinica Chimica Acta
IS - 3
ER -