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PMID: 11560492 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

An engineered transthyretin monomer that is nonamyloidogenic, unless it is partially denatured.

Biochemistry ·Vol. 40 ·No. 38 ·2001-09-25 ·Pages 11442-52

Jiang X, Smith CS, Petrassi HM, Hammarström P, White JT, Sacchettini JC, Kelly JW

Abstract

Transthyretin (TTR) is a soluble human plasma protein that can be converted into amyloid by acid-mediated dissociation of the homotetramer into monomers. The pH required for disassembly also results in tertiary structural changes within the monomeric subunits. To understand whether these tertiary structural changes are required for amyloidogenicity, we created the Phe87Met/Leu110Met TTR variant (M-TTR) that is monomeric according to analytical ultracentrifugation and gel filtration analyses and nonamyloidogenic at neutral pH. Results from far- and near-UV circular dichroism spectroscopy, one-dimensional proton NMR spectroscopy, and X-ray crystallography, as well as the ability of M-TTR to form a complex with retinol binding protein, indicate that M-TTR forms a tertiary structure at pH 7 that is very similar if not identical to that found within the tetramer. Reducing the pH results in tertiary structural changes within the M-TTR monomer, rendering it amyloidogenic, demonstrating the requirement for partial denaturation. M-TTR exhibits stability toward acid and urea denaturation that is nearly identical to that characterizing wild-type (WT) TTR at low concentrations (0.01-0.1 mg/mL), where monomeric WT TTR is significantly populated at intermediate urea concentrations prior to the tertiary structural transition. However, the kinetics of denaturation and fibril formation are much faster for M-TTR than for tetrameric WT TTR, particularly at near-physiological concentrations, because of the barrier associated with the tetramer to folded monomer preequilibrium. These results demonstrate that the tetramer to folded monomer transition is insufficient for fibril formation; further tertiary structural changes within the monomer are required.

MeSH Terms
Amino Acid Substitution Amyloid/metabolism Binding Sites Crystallography, X-Ray/methods Dimerization Drug Stability Fluorescent Dyes Guanidine Humans Hydrogen-Ion Concentration Macromolecular Substances Models, Molecular Mutagenesis, Site-Directed Nuclear Magnetic Resonance, Biomolecular/methods Prealbumin/chemistry,metabolism,ultrastructure Protein Denaturation Protein Structure, Secondary Recombinant Proteins/chemistry,metabolism,ultrastructure Spectrometry, Fluorescence Tryptophan/analysis Ultracentrifugation/methods Urea
Chemicals
Amyloid Fluorescent Dyes Macromolecular Substances Prealbumin Recombinant Proteins Tryptophan Urea Guanidine
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Jiang X
Department of Chemistry and The Skaggs Institute of Chemical Biology, The Scripps Research Institute, La Jolla, California 92037, USA.
Smith C S
Petrassi H M
Hammarström P
White J T
Sacchettini J C
Kelly J W
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
2001-09-25
Pages
11442-52
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Grants
NIDDK NIH HHS · DK46335 · United States
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