Specific VDAC inhibitors: phosphorothioate oligonucleotides

被引:0
作者
C.A. Stein
Marco Colombini
机构
[1] Montefiore Medical Center,Albert Einstein–Montefiore Cancer Center, Department of Oncology
[2] University of Maryland,Department of Biology
来源
Journal of Bioenergetics and Biomembranes | 2008年 / 40卷
关键词
Mitochondria; Outer membrane; Blocker; G3139; Randomer;
D O I
暂无
中图分类号
学科分类号
摘要
VDAC channels are ancient, highly-conserved voltage-gated channels in the mitochondrial outer membrane. They are the pathways by which metabolites travel between the cytosol and mitochondria. They are involved in the apoptotic process and probably other functions as well. The lack of specific inhibitors has hampered research in the past but now phosphothioate oligonucleotides can serve this function. These molecules were generated to be stable in the cytosol of cells but, unlike the oligonucleotides with the physiological phosphodiester linkage, these have the ability to bind to and block VDAC channels. They are potent, specific, and available commercially. At 1 μM concentration they block VDAC channels in mitochondria but do not affect the respiration complexes, the adenine nucleotide translocator or the ATP synthase.
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收藏
页码:157 / 162
页数:5
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