Characterization, cell-free synthesis and processing of apolipoprotein A-I of rat high-density lipoproteins

Abstract

Rat apolipoprotein A-I (apoA-I) was isolated from delipidated high-density lipoproteins by sequential chromatography on Sepharcyl S-200 and Sephadex G-150 columns in guanidine buffer. The purified protein had an apparent MW of 27,000 and was homogeneous by NaDodSO4 (sodium dodecyl sulfate) and urea gel electrophoresis. Its amino acid composition was similar to that previously reported by Swaney et al. Microsequencing yielded an N-terminal sequence of Asp-Glu-Pro-Pro-Val-(Ser)-Glu-. Rabbit antisera were generated against the purified rat apoA-I and were shown to be monospecific against the protein by immunodiffusion and immunoelectrophoresis. Total poly(A) RNA was isolated from the rat liver by extraction in guanidine hydrochloride buffer and oligo(dT)-cellulose chromatography. In vitro translation of the RNA was performed in both wheat germ and nuclease-treated reticulocyte lysate systems, using [35S]Met as the radioactive amino acid precursor. Immunoreactive 35S-labeled apoA-I synthesized in vitro was precipitated by a rabbit antirat apoA-I serum. It was analyzed on an NaDodSO4-acrylamide slab gel and visualized by fluorography. The in vitro product had an apparent MW of 28,500, being larger than the authentic plasma protein by approximately 1500 daltons. When translation was performed in the presence of dog pancreatic microsomal membranes, the immunoprecipitable material was cotranslationally cleaved to a product identical in size (Mr 27,000) with plasma apoA-I. A putative precursor to rat apoA-I, designated preapoA-I was thus synthesized in vitro. The preapoA-I was processed in a cell-free system to its mature plasma counterpart by the addition of exogenous microsomal membranes.