Adaptive translocation: the role of hydrogen bonding and membrane potential in the uptake of guanidinium-rich transporters into cells

被引:238
作者
Rothbard, JB [1 ]
Jessop, TC [1 ]
Wender, PA [1 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
关键词
arginine-rich transporters; membrane potential; ion pairs; drug delivery; protein translocation; endocytosis; HIV tat; Antennapedia; FGF;
D O I
10.1016/j.addr.2004.10.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A mechanistic hypothesis is presented for how water-soluble guanidinium-rich transporters attached to small cargoes (MW ca. < 3000) can migrate across the non-polar lipid membrane of a cell and enter the cytosol. Positively charged and watersoluble, arginine oligomers can associate with negatively charged, bidentate hydrogen bond acceptor groups of endogenous membrane constituents, leading to the formation of membrane-soluble ion pair complexes. The resultant less polar, ion pair complexes partition into the lipid bilayer and migrate in a direction, and with a rate, influenced by the membrane potential. The complex dissociates on the inner leaf of the membrane and the transporter conjugate enters the cytosol. This mechanism could also be involved in the translocation of guanidinium-rich molecules that are endocytosed due to their size or the conditions of the assay, across the endosomat membrane. (c) 2005 Elsevier B.V All rights reserved.
引用
收藏
页码:495 / 504
页数:10
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