» Articles » PMID: 6947238

Protein Variations Associated with Lesch-Nyhan Syndrome

Overview
Specialty Science
Date 1981 Oct 1
PMID 6947238
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Patients having Lesch--Nyhan syndrome were studied by using enzymatic, immunologic, and two-dimensional electrophoretic techniques. Four hundred proteins were analyzed on each two-dimensional electrophoretogram for positional or quantitative variation. In autoradiograms of lymphocytes stimulated with phytohemagglutinin, there were 11 quantitative differences found in all patients that were significant at the 2P less than 0.01 level. A significant quantitative difference was also found in an analysis of silver-stained gels of unstimulated lymphocytes. Patients had trace amounts of erythrocyte hypoxanthine phosphoribosyl transferase (HPRT) activity and trace or no immunoprecipitable HPRT. However, HPRT was observed in silver-stained erythrocyte electrophoretograms and in autoradiograms from phytohemagglutinin-stimulated lymphocytes. Unstimulated lymphocytes contained 65% of the control HPRT concentration. Currently, the technology of two-dimensional electrophoresis detects a fraction of the total cellular proteins and defective proteins may not show electrophoretic alterations. However, specific secondary changes in other polypeptides may be observed and, when catalogued, will serve as an aid in the diagnosis and understanding of the pathophysiology of metabolic diseases.

Citing Articles

Amplification of hypoxanthine-guanine phosphoribosyltransferase genes in chromosome-mediated gene transferents.

Linder S, Coleman A, Eisenstadt J Mol Cell Biol. 1984; 4(4):618-24.

PMID: 6717438 PMC: 368767. DOI: 10.1128/mcb.4.4.618-624.1984.


Human lymphocyte polymorphisms detected by quantitative two-dimensional electrophoresis.

Goldman D, Merril C Am J Hum Genet. 1983; 35(5):827-37.

PMID: 6577787 PMC: 1685808.


Identification of a yellow gene-specific protein in Drosophila melanogaster by two-dimensional gel electrophoresis.

Nash W, Kamerow H, Merril C Biochem Genet. 1983; 21(11-12):1135-42.

PMID: 6422926 DOI: 10.1007/BF00488465.


Comparison of small proteoglycans from skin fibroblasts and vascular smooth-muscle cells.

Rauch U, Glossl J, Kresse H Biochem J. 1986; 238(2):465-74.

PMID: 3800948 PMC: 1147158. DOI: 10.1042/bj2380465.


Human neutrophil plasma membrane. Specific labelling, topological distribution of proteins and surface antigen detection.

Lacal P, Mollinedo F, Larraga V Mol Cell Biochem. 1987; 77(2):161-71.

PMID: 3325821 DOI: 10.1007/BF00221925.


References
1.
Seegmiller J, Rosenbloom F, Kelley W . Enzyme defect associated with a sex-linked human neurological disorder and excessive purine synthesis. Science. 1967; 155(3770):1682-4. DOI: 10.1126/science.155.3770.1682. View

2.
LOWRY O, ROSEBROUGH N, FARR A, RANDALL R . Protein measurement with the Folin phenol reagent. J Biol Chem. 1951; 193(1):265-75. View

3.
Sorensen L, Benke P . Biochemical evidence for a distinct type of primary gout. Nature. 1967; 213(5081):1122-3. DOI: 10.1038/2131122b0. View

4.
Rosenbloom F, HENDERSON J, CALDWELL I, Kelley W, Seegmiller J . Biochemical bases of accelerated purine biosynthesis de novo in human fibroblasts lacking hypoxanthine-guanine phosphoribosyltransferase. J Biol Chem. 1968; 243(6):1166-73. View

5.
Kelley W, Greene M, Rosenbloom F, HENDERSON J, Seegmiller J . Hypoxanthine-guanine phosphoribosyltransferase deficiency in gout. Ann Intern Med. 1969; 70(1):155-206. DOI: 10.7326/0003-4819-70-1-155. View