New insights into the interaction of emodin with lipid membranes

Abstract

Emodin is a natural anthraquinone derivative found in nature, widely known as an herbal medicine. Here, the partition, location, and interaction of emodin with lipid membranes of 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) are experimentally investigated with different techniques. Our studies have considered the neutral form of emodin (EMH) and its anionic/deprotonated form (EM^-), and their interaction with a more and less packed lipid membrane, DMPC at the gel and fluid phases, respectively. Though DSC results indicate that the two species, EMH and EM^-, similarly disrupt the packing of DMPC bilayers, spin labels clearly show that EMH causes a stronger bilayer disruption, both in gel and fluid DMPC. Fluorescence spectroscopy shows that both EMH and EM^- have a high affinity for DMPC: the binding of EM^- to both gel and fluid DMPC bilayers was found to be quite similar, and similar to that of EMH to gel DMPC, K_p = (1.4 ± 0.3)x10³. However, EMH was found to bind twice more strongly to fluid DMPC bilayers, K_p = (3.2 ± 0.3)x10³. Spin labels and optical absorption spectroscopy indicate that emodin is located close to the lipid bilayer surface, and suggest that EM^- is closer to the lipid/water interface than EMH, as expected. The present studies present a relevant contribution to the current understanding of the effect the two species of emodin, EMH and EM^-, present on different microregions of an organism, as local pH values can vary significantly, can cause in a neutral lipid membrane, either more or less packed, liked gel and fluid DMPC, respectively, and could be extended to lipid domains of biological membranes.

Keywords: Differential scanning calorimetry; ESR spectroscopy; Emodin; Lipid bilayer; Lipid partition coefficient; Optical spectra.