Membrane potential stimulates ADP import and ATP export by the mitochondrial ADP/ATP carrier due to its positively charged binding site

被引:1
|
作者
Mavridou, Vasiliki [1 ]
King, Martin S. [1 ]
Bazzone, Andre [2 ]
Springett, Roger [3 ]
Kunji, Edmund R. S. [1 ]
机构
[1] Univ Cambridge, MRC Mitochondrial Biol Unit, Cambridge Biomed Campus, Keith Peters Bldg, Cambridge CB2 0XY, England
[2] Nanion Technol GmbH, Ganghoferstr 70A, D-80339 Munich, Germany
[3] CellSpex, Kettering NN14 6GX, Northants, England
来源
SCIENCE ADVANCES | 2024年 / 10卷 / 44期
基金
英国医学研究理事会;
关键词
SUBSTRATE-SPECIFICITY; TRANSPORT; MECHANISM; STATE; ATRACTYLOSIDE; TRANSLOCATION; PROTEINS; STEP;
D O I
10.1126/sciadv.adp7725
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The mitochondrial adenosine 5 '-diphosphate (ADP)/adenosine 5 '-triphosphate (ATP) carrier imports ADP into the mitochondrion and exports ATP to the cell. Here, we demonstrate that 3.3 positive charges are translocated with the negatively charged substrate in each transport step. They can be assigned to three positively charged residues of the central substrate-binding site and two asparagine/arginine pairs. In this way, the membrane potential stimulates not only the ATP4- export step, as a net -0.7 charge is transported, but also the ADP3- import step, as a net +0.3 charge is transported with the electric field. These positive charge movements also inhibit the import of ATP and export of ADP in the presence of a membrane potential, allowing these nucleotides to be maintained at high concentrations in the cytosol and mitochondrial matrix to drive the hydrolysis and synthesis of ATP, respectively. Thus, this is the mechanism by which the membrane potential drives adenine nucleotide exchange with high directional fluxes to fuel the cellular processes.
引用
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页数:12
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