Issue 8, 2014

Studies on the isolated mitochondrial damage induced by α-tocopheryl succinate and its interactions with human serum albumin

Abstract

α-tocopheryl succinate (α-TOS), a redox-inactive vitamin E analogue, holds great promise for selectively triggering mitochondrial apoptosis in tumor cells. In this paper, in order to better understand the biophysical basis of α-TOS under biological conditions, the effects of α-TOS at high concentrations on the function of mitochondria and its interactions with human blood protein (human serum albumin, HSA) were investigated. We found that α-TOS with high concentration not only caused inhibition of mitochondrial respiration and mitochondrial permeability transition (MPT), but also strongly disturbed the mitochondrial membrane and ultrastructure. These results suggest that mitochondria are organelles that are very sensitive to α-TOS-induced stress, and the mechanism of damage to mitochondria may be due to MPT and impairing of the respiratory chain. In addition, it has been also demonstrated that α-TOS possesses moderate binding affinity to HSA in site I due to the formation of the α-TOS–HSA complex by hydrophobic, van der Waals and hydrogen bond forces. These results will help us learn more about biophysical properties of α-TOS at subcellular (mitochondria) and biomacromolecular (HSA) levels.

Graphical abstract: Studies on the isolated mitochondrial damage induced by α-tocopheryl succinate and its interactions with human serum albumin

Article information

Article type
Paper
Submitted
28 Oct 2013
Accepted
04 Dec 2013
First published
05 Dec 2013

RSC Adv., 2014,4, 3913-3919

Studies on the isolated mitochondrial damage induced by α-tocopheryl succinate and its interactions with human serum albumin

D. Li, H. He, B. Lin, Z. Xu, F. Jiang and Y. Liu, RSC Adv., 2014, 4, 3913 DOI: 10.1039/C3RA46172F

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