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Assays / Genetic
Enzymes / [35S]-Cystine
Incorporation
PRINCIPLE OF METHOD: Cultured cells or
fragments of chorionic villi are incubated in tissue culture medium
containing [35S]-L-cystine. In normal cells the
labelled amino acid enters lysosomes and diffuses out again. In
cells from cystinosis patients, however, it remains within lysosomes
due to lack of a transporter required for its exit. When the cells
are harvested, protein is removed by precipitation and the soluble
fraction run on a thin-layer chromatogram an excess of label is
found in the position of cystine. The harvested cells are in fact
suspended in a buffer containing N-ethylmaleimide (NEM) which binds
to free -SH compounds. The glutathione-NEM complex thus formed is
also separated in the chromatogram and counted. Final results are
expressed as a ratio cystine: glutathione-NEM and also as cystine
incorporated per ìg protein.
USES AND LIMITATIONS OF THE METHOD: The
method is used to diagnose cystinosis both postnatally and
prenatally. In fact the use for postnatal diagnosis has been largely
superseded by an alternative method employing a cystine binding
protein which can be used with freshly prepared white cells and
is more rapid and less costly than the isotope incorporation method
(available in the Paediatrics Department laboratory, Guy's
Hospital). However, the isotope method is still routinely used for
prenatal diagnosis. Heterozygote detection is not offered using
this method.
SPECIMEN REQUIREMENTS: Fibroblasts cultured
from a skin biopsy are 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 at the laboratory
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.
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