HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC ANALYSIS OF BIOLOGICAL AND CHEMICAL HEME POLYMERIZATION

Citation
Bj. Berger et al., HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC ANALYSIS OF BIOLOGICAL AND CHEMICAL HEME POLYMERIZATION, Analytical biochemistry, 231(1), 1995, pp. 151-156
Citations number
14
Categorie Soggetti
Biology
Journal title
ISSN journal
00032697
Volume
231
Issue
1
Year of publication
1995
Pages
151 - 156
Database
ISI
SICI code
0003-2697(1995)231:1<151:HLAOBA>2.0.ZU;2-X
Abstract
Free hematin can be converted to a stable polymer both chemically, by heating hematin in acid suspensions, or biologically, in the food vacu oles of malaria. A high-performance liquid chromatographic assay has b een developed which can separate and quantitate both free hematin and the polymer (beta-hematin), based on the differential solubility of th e two compounds. Ion-pair reverse-phase chromatography, utilizing tetr amethylammonium chloride and heptane sulfonate as the ion-pair agents in the presence of 40% acetonitrile, was performed on a polymeric-resi n-based column with a phenyl bonded phase. Initiating the runs at pH 2 .5 led to elution only of the free hematin, and a subsequent shift to pH 12.0 converted the beta-hematin back to hematin which then eluted s eparately. The method was found to have a linear range of detection fr om 78 pmol to 20 nmol injected hematin and intra- and interday variati ons of 9.71 and 12.46%, respectively. The assay was used to study seve ral basic aspects of heme polymerization in vitro, including effects o f hematin and beta-hematin concentration on the rate of polymerization . (C) 1995 Academic Press, Inc.