|
Assays / Genetic
Enzymes / Glucosamine
N-Acetyltransferase
Principle Of Method:
The transfer of an acetyl group from acetyl-CoA to 14C(U)glucosamine
is measured by determining the amount of radioactivity eluted from
a Dowex-50 (H+) column. Unreacted [14C]-glucosamine
remains bound. The glucosamine in this reaction serves as a substitute
for glucosamine at the non-reducing end of heparan sulphate molecules
which is the natural substrate for the enzyme. Use of glucosamine
greatly facilitates assay of the enzyme. An alternative fluorogenic
substrate, 4-methylumbelliferyl-a-D-glucosaminide
is available but the method is not yet running in the SAS laboratory.
Uses And Limitations Of The Method:
Deficiency of the N-acetyltransferase (full name acetyl-CoA:a-glucosaminide
N-acetyltransferase) is the primary defect in Sanfilippo
disease type C (MPS IIIC). Its natural
function is to acetylate a-linked
glucosamine residues in heparan sulphate after they have been de-N-sulphated
by heparan sulphamidase so that a-N-acetylglucosaminidase
can then cleave them. In its absence there is storage of heparan
sulphate in the tissues and excess excretion in the urine. The deficiency
can be shown in white cells or fibroblasts, and the assay is usually
run after excess heparan sulphaturia has been found. MPS IIIC is
rare in the UK but native-born cases are known. It is probably rather
more common in continental Europe. Prenatal diagnosis is possible
by analysis of chorionic villi or cultured amniotic cells; when
amniocentesis is performed investigation of the GAG pattern in the
supernatant fluid may assist in the diagnosis. Heterozygote detection
is not offered by the laboratory.
Specimen Requirements:
For preliminary testing, blood. 5 ml lithium heparin (orange
capped tube) unseparated and unfrozen. Send at room temperature
to arrive at the laboratory
within 24h of venepuncture. For follow-up, fibroblasts cultured
from a skin biopsy may be needed. Biopsy material should
be collected aseptically into a sterile bottle containing tissue
culture medium (available from the laboratory), and sent at room
temperature to arrive within 24 hours. Biopsies for tissue culture
should not be frozen. Fibroblast cultures established
in other laboratories should be sent in plastic 25 cm2
flasks filled with medium.
THE LABORATORY RECOMMENDS USE OF A COURIER SERVICE
OR ROYAL MAIL SPECIAL DELIVERY FOR SENDING ALL SPECIMENS TO THE
LABORATORY.
Back to Lysosomal
Storage Disorders Index
Back to Alphabetical List of
Assays Available
|