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Correspondence to:
Mika Ala-Korpela.
Recent evidence suggests that fusion of low density lipoprotein (LDL) particles is a key process in the initial accumulation of lipid in the arterial intima. In order to gain a better understanding of this early event in the development of atherosclerosis, it would thus be necessary to characterize the process of LDL fusion in detail. Such studies, however, pose severe methodological difficulties, such as differentiation of particle fusion from aggregation. In this paper we describe the use of novel methodology, based on 1H NMR spectroscopy, to study lipoprotein particle fusion. To test the methodology, we chose proteolytic fusion of LDL particles, an in vitro model that has been well characterized in our laboratory. The spectroscopic data suggested that proteolysis of LDL with
The 1H NMR methodology developed is sensitive to and specific for low density lipoprotein (LDL) fusion and may also allow for studies of the fate of LDL particles in other in vitro preparations that mimic the arterial interactions in vivo.Ala-Korpela, M., M. O. Pentikäinen. A. Korhonen, T. Hevonoja, J. Lounila, and P. T. Kovanen. Detection of low density lipoprotein particle fusion by proton nuclear magnetic resonance spectroscopy. J. Lipid Res. 1998. 39: 17051712.
Supplementary key words:
fusion, lipid accumulation, low density lipoprotein, nuclear magnetic resonance spectroscopy, proteolysis
Copyright © 1998 by Lipid Research, Inc.
Original Article
Detection of low density lipoprotein particle fusion by proton nuclear magnetic resonance spectroscopy
Mika Ala-Korpelaa,
Markku O. Pentikäinena,
Ari Korhonenb,
Tiia Hevonojaa,
Juhani Lounilab, and
Petri T. Kovanena
a Wihuri Research Institute, Kalliolinnantie 4, FIN-00140 Helsinki, Finland
b Department of Physical Sciences, NMR Research Group, University of Oulu, P. O. Box 333, FIN-90571 Oulu, Finland
-chymotrypsin induced slow initiation of fusion, which was followed by particle fusion at an increased rate. Moreover, 1H NMR spectroscopic data on different kinds of LDL interactions, for example, when LDL formed aggregates with antibodies against human apolipoprotein B-100, were obtained and compared with the electron microscopic characteristics of these preparations. An important finding was that limited aggregation of LDL particles did not disturb the 1H NMR spectroscopic parameters used for the detection of particle fusion and preserved the physico-chemical information on the particles. ![]()
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