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PMID: 3360781 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Human apolipoprotein E3 in aqueous solution. I. Evidence for two structural domains.

The Journal of biological chemistry ·Vol. 263 ·No. 13 ·1988-05-05 ·Pages 6240-8

Wetterau JR, Aggerbeck LP, Rall SC, Weisgraber KH

Abstract

The stability and structure of human apolipoprotein (apo) E3 in aqueous solution were investigated by guanidine HCl denaturation and limited proteolysis. The guanidine HCl denaturation curve, as monitored by circular dichroism spectroscopy, was biphasic; the two transition midpoints occurred at 0.7 and 2.5 M guanidine HCl, indicating that there are stable intermediate structures in the unfolding of apoE. Limited proteolysis of apoE with five enzymes demonstrated two proteolytically resistant regions, an amino-terminal domain (residues 20-165) and a carboxyl-terminal domain (residues 225-299). The region between them was highly susceptible to proteolytic cleavage. Because of their similarity to the proteolytically resistant regions, the amino-terminal (residues 1-191) and carboxyl-terminal (residues 216-299) thrombolytic fragments of apoE were used as models for the two domains. Guanidine HCl denaturation of the carboxyl- and amino-terminal fragments gave transition midpoints of 0.7 and 2.4 M guanidine HCl, respectively. The results establish that the two domains identified by limited proteolysis correspond to the two domains detected by protein denaturation experiments. Therefore, the thrombolytic fragments are useful models for the two domains. The free energies of denaturation calculated from the denaturation curves of intact apoE or the model domains were approximately 4 and 8-12 kcal/mol for the carboxyl- and amino-terminal domains, respectively. The value for the carboxyl-terminal domain is similar to those of previously characterized apolipoproteins, whereas the value for the amino-terminal domain is considerably higher and resembles those of soluble globular proteins. These studies suggest that, in aqueous solution, apoE is unlike other apolipoproteins in that it contains two independently folded structural domains of markedly different stabilities: an amino-terminal domain and a carboxyl-terminal domain, separated by residues that may act as a hinge region.

MeSH Terms
Algorithms Apolipoprotein E3 Apolipoproteins E Circular Dichroism Electrophoresis, Polyacrylamide Gel Guanidine Guanidines Humans Hydrolysis Protein Conformation Protein Denaturation Solutions Time Factors
Chemicals
Apolipoprotein E3 Apolipoproteins E Guanidines Solutions Guanidine
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Wetterau J R
Gladstone Foundation Laboratories for Cardiovascular Disease, University of California, San Francisco 94140-0608.
Aggerbeck L P
Rall S C
Weisgraber K H
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1988-05-05
Pages
6240-8
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NHLBI NIH HHS · HL 18577-11 · United States
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