Hioppe-Seyler's Z. Physiol. Chem.
Bd. 363, S.425-430, April 1982
Synthesis and Processing of Arylsulfatase A in Human Skin Fibroblasts
Abdul WAHEED*, Andrej HASILIK and Kurt VON FIGURA
Physiologisch-Chemisches Institut der Universität Münster
(Received 28 December 1981)
Summary: Biosynthesis of arylsulfatase A in
normal and mutant human fibroblasts was
studied by growing cells in the presence of L -
[4,5-
3
H]leucine or [2-
3
H]mannose, isolation of
labelled arylsulfatase A by immune precipitation
and visualization of electrophoretically separated
polypeptides by fluorography. Arylsulfatase A
was synthesized as a precursor with a mean ap-
parent molecular mass of 62 kDa. Intracellularly
the precursor was converted into a 60.5 kDa poly-
peptide within a chase period of 1 to 7 days. The
60.5 kDa product in polyacrylamide corresponded
to one of two polypeptides present in arylsul-
fatase A isolated from human placenta. In fibro-
blasts from a patient with metachromatic leuko-
dystrophy no immune precipitable polypeptides
of arylsulfatase A were detected. In normal fibro-
blasts less than 10% of the precursor of arylsul-
fatase A was secreted into the medium, whereas
in mucolipidosis II fibroblasts and in control
fibroblasts grown in the presence of NH4C1 up to
90% of the precursor of arylsulfatase A, appeared
in the medium and remained there without change
in the apparent molecular mass for at least
7 days. Arylsulfatase A polypeptides appear to
contain two carbohydrate side chains. In about
90% of the polypeptides both side chains are
cleaved by endo-ß-yV-acetylglucosaminidase H,
whereas in the remaining chains one of the two
oligosaccharides is not cleaved.
Synthese und höhermolekulare Vorstufen (processing) von Arylsulfatase A in menschlichen
Hautfibrob lasten
Zusammenfassung: Arylsulfatase A wurde durch
Immunpräzipitation aus Zell- und Mediumextrak-
ten von normalen und mutanten menschlichen
Fibroblasten isoliert, die in Gegenwart von L-
[4,5-
3
H]Leucin bzw. [2-
3
H]Mannose inkubiert
worden waren. Die Immunpräzipitate wurden
solubilisiert und die radioaktiven Polypeptide
nach gelelektrophoretischer Auftrennung durch
Fluorographie sichtbar gemacht. Arylsulfatase
A wird als ein Polypeptid mit einer mittleren
Molekularmasse von 62.5 kDa synthetisiert. Diese
62.5-kDa-Form der Arylsulfatase ist eine Vor-
stufe und wird innerhalb von 7 Tagen zu einem
Polypeptid mit einer mittleren Molekularmasse
von 60.5 kDa verkürzt, das einer der beiden Aryl-
sulfatase-A-Formen aus menschlicher Plazenta
Enzymes:
Arylsulfatase A, aryl-sulfate sulfohydrolase (EC 3.1.6.1);
Endo-j3-7V-acetylglucosaminidase H, mannosyl-glycoprotein l,4-7V-acetamidodeoxy-/3-D-glycohydrolase (EC 3.2.1.96).
* Recipient of an Alexander von Humboldt fellowship
00184888/82/0363-0425$02.00
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