ABSTRACT
BACKGROUND & AIMS: Many putative pronucleating proteins have been isolated from the biliary concanavalin A (con A)-binding fraction. The pronase resistance of the overall nucleating-promoting activity was almost never taken into consideration. The aim of this study was to identify the major pronase-resistant con A-binding glycoproteins. METHODS: Pronase-treated and -untreated con A-binding glycoproteins were separated on a Superose 12 gel permeation column (Pharmacia, Uppsala, Sweden) and tested in a crystal growth assay. Proteins were identified by amino-terminal sequencing. RESULTS: Con A-binding pronucleating activity eluted in two peaks on the Superose column. This activity was unaltered after pronase treatment. Activity peak I contained too little protein to allow amino-terminal sequencing. In activity peak II, the major pronase-resistant con A-binding glycoproteins were identified as alpha 1-antitrypsin and alpha 1-antichymotrypsin. The 130-kilodalton nucleation promoter was identified as aminopeptidase N, but the full pronase resistance of this protein, reported earlier, was not confirmed. Immunoabsorptive removal of alpha 1-antitrypsin and alpha 1-antichymotrypsin and immunopurification showed that only alpha 1-antichymotrypsin had pronucleating activity. CONCLUSIONS: The pronase resistance of the nucleating-promoting activity of the con A-binding glycoprotein fraction was confirmed. An important part of this activity could be attributed to alpha 1-antichymotrypsin. It is an acute-phase protein, as are many other pronucleating proteins, which might indicate a general mechanism of action in gallstone formation.
Subject(s)
Bile/metabolism , Cholesterol/physiology , Glycoproteins/physiology , Pronase/pharmacology , Adult , Aged , Amino Acid Sequence , Bile/drug effects , Chromatography, Gel , Concanavalin A , Crystallization , Drug Resistance , Enzyme-Linked Immunosorbent Assay , Female , Glycoproteins/genetics , Humans , Male , Middle Aged , Molecular Sequence Data , Pronase/genetics , Sepharose , alpha 1-Antichymotrypsin/physiology , alpha 1-Antitrypsin/physiologyABSTRACT
We present an assay to study cholesterol crystallization that is fast, facile, and highly reproducible. Cholesterol crystallization from metastable vesicles was induced upon addition of bile salts and depended on the hydrophobicity of the bile salt used and the cholesterol-to-phospholipid ratio of the vesicles. Bile salt-induced crystallization was stimulated upon addition of Con A-binding glycoproteins (CABGs), comparable to the results of the same CABGs in a crystal growth assay. The onset time and total measuring time, however, were much shorter. This assay might, moreover, provide a tool to study the mechanism of cholesterol crystallization in more detail.
Subject(s)
Cholesterol/chemistry , Bile/chemistry , Cholelithiasis/chemistry , Crystallization , Humans , In Vitro Techniques , Micelles , Microscopy, ElectronABSTRACT
In this study, the interaction of mucin and concanavalin A-binding proteins isolated from human bile with cholesterol/phospholipid vesicles was investigated. Using resonance energy transfer assays originally developed by Struck, Hoekstra and Pagano [(1981) Biochemistry 20, 4093-4099], no significant protein-induced fusion or aggregation of vesicles was demonstrated. Instead of fusion, these proteins induced destabilization of cholesterol/phospholipid vesicles, as monitored by release of entrapped carboxyfluorescein. A good correlation (rho = 0.81) was obtained between the extent of leakage and the nucleation-promoting activity of the concanavalin A-binding proteins. We conclude that aggregation or fusion of cholesterol/phospholipid vesicles is not an obligatory step in cholesterol crystallization. Biliary protein-induced crystallization seems to be preceded by vesicle disruption.
