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PMID: 3707586 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

Hereditary cerebral amyloid angiopathy: the amyloid fibrils contain a protein which is a variant of cystatin C, an inhibitor of lysosomal cysteine proteases.

Biochemical and biophysical research communications ·Vol. 136 ·No. 2 ·1986-04-29 ·Pages 548-54

Ghiso J, Pons-Estel B, Frangione B

Abstract

Hereditary Cerebral Hemorrhage With Amyloidosis is an autosomal dominant form of amyloidosis restricted to the cerebral vasculature. We have previously demonstrated that the amyloid protein subunit is similar to Cystatin C (or gamma-trace), an inhibitor of lysosomal cysteine proteinases, and homologous to kininogens. High pressure liquid chromatography tryptic fingerprint analysis was developed to distinguish Cystatin C from the amyloid protein. Moreover, we isolated and sequenced tryptic peptides in which the differences were detected. The data prove that the amyloid protein is 10 residues shorter than Cystatin C and has one amino acid substitution at residue 58.

MeSH Terms
Amino Acid Sequence Amino Acids/analysis Amyloid/analysis,metabolism Amyloidosis/complications,genetics,metabolism Cerebral Hemorrhage/etiology Chromatography, High Pressure Liquid Cystatin C Cystatins Humans Macromolecular Substances Peptide Fragments/metabolism Proteins/analysis Proteinuria Trypsin/metabolism
Chemicals
Amino Acids Amyloid CST3 protein, human Cystatin C Cystatins Macromolecular Substances Peptide Fragments Proteins Trypsin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Ghiso J
Pons-Estel B
Frangione B
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1986-04-29
Pages
548-54
Language
English
Region
United States
NLM ID
0372516
Subset
IM
Grants
NIA NIH HHS · AG 05891 · United States
NIADDK NIH HHS · AM 01431 · United States
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