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PMID: 5073741 Published · ppublish English Journal Article

Thio reduction of human 2 -macroglobulin. The subunit structure.

The Biochemical journal ·Vol. 127 ·No. 1 ·1972-03-00 ·Pages 187-97

Jones JM, Creeth JM, Kekwick RA

Abstract

1. Human alpha(2)-macroglobulin was prepared from a fraction obtained during the large-scale separation of normal human plasma proteins for clinical use. 2. Sedimentation-equilibrium measurements indicated a molecular weight of 725000. A value of 18.1S was obtained for s(0) (20,w). 3. The dissociation that occurs in the pH range 4.5-2.5 and in the region of neutrality in urea-containing solutions is consistent with a dimeric structure of the molecule. 4. The effects of the thiol reagents mercaptoethanol, mercaptoethylamine and N-acetylcysteine were investigated over a range of experimental conditions. Distinct components having sedimentation coefficients of 15, 12 and 8.5S were identified. 5. Conditions were found under which limited reduction with thiol liberated a subunit with a molecular weight approximately one-quarter of that of the intact molecule. This subunit retains the serological specificity of the whole molecule.

MeSH Terms
Acetylcysteine Blood Proteins/isolation & purification Chemical Phenomena Chemistry Humans Hydrogen-Ion Concentration Macroglobulins Mercaptoethanol Mercaptoethylamines Molecular Weight Optical Rotatory Dispersion Oxidation-Reduction Urea
Chemicals
Blood Proteins Macroglobulins Mercaptoethylamines Mercaptoethanol Urea Acetylcysteine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Jones J M
Creeth J M
Kekwick R A
References (20)
20 references, click to expand
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Article Info
Journal
The Biochemical journal
Abbr.
Biochem J
ISSN
0264-6021
Published
1972-03-00
Pages
187-97
Language
English
Region
England
NLM ID
2984726R
PMCID
PMC1178573
Subset
IM
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