Institute of Electron Devices and Circuits, University of Ulm, 89069 Ulm, Germany.
Department of Chemistry, Faculty of Philosophy, Sciences and Letters at Ribeirão Preto, University of São Paulo, Ribeirão Preto 14040-901, SP, Brazil.
Biosensors (Basel). 2022 Jul 14;12(7):525. doi: 10.3390/bios12070525.
This report describes the innovative application of high sensitivity Boron-doped nanocrystalline diamond microelectrodes for tracking small changes in Ca concentration due to binding to Annexin-A5 inserted into the lipid bilayer of liposomes (proteoliposomes), which could not be assessed using common Ca selective electrodes. Dispensing proteoliposomes to an electrolyte containing 1 mM Ca resulted in a potential jump that decreased with time, reaching the baseline level after ~300 s, suggesting that Ca ions were incorporated into the vesicle compartment and were no longer detected by the microelectrode. This behavior was not observed when liposomes (vesicles without AnxA5) were dispensed in the presence of Ca. The ion transport appears Ca-selective, since dispensing proteoliposomes in the presence of Mg did not result in potential drop. The experimental conditions were adjusted to ensure an excess of Ca, thus confirming that the potential reduction was not only due to the binding of Ca to AnxA5 but to the transfer of ions to the lumen of the proteoliposomes. Ca uptake stopped immediately after the addition of EDTA. Therefore, our data provide evidence of selective Ca transport into the proteoliposomes and support the possible function of AnxA5 as a hydrophilic pore once incorporated into lipid membrane, mediating the mineralization initiation process occurring in matrix vesicles.
本报告介绍了高灵敏度掺硼纳米金刚石微电极的创新应用,该电极可用于跟踪由于结合到插入脂质双层的膜联蛋白 A5(脂质体中的亲水性通道)而导致的 Ca 浓度的微小变化,而这是使用常见的 Ca 选择性电极无法评估的。将含有 1mM Ca 的电解液中的亲脂体(无 AnxA5 的脂质体)分配到电解液中会导致电位跃变,该电位跃变随时间降低,在~300s 后达到基线水平,表明 Ca 离子已进入囊泡腔室,不再被微电极检测到。当在 Ca 存在下分配脂质体(没有 AnxA5 的囊泡)时,不会观察到这种行为。这种离子传输似乎是 Ca 选择性的,因为在存在 Mg 的情况下分配亲脂体不会导致电位下降。实验条件进行了调整以确保 Ca 过量,从而证实电位降低不仅归因于 Ca 与 AnxA5 的结合,而且归因于离子向亲脂体腔室的转移。加入 EDTA 后,Ca 摄取立即停止。因此,我们的数据提供了证据证明 Ca 选择性地转运到亲脂体中,并支持膜联蛋白 A5 一旦整合到脂质膜中可能作为亲水性孔的功能,从而介导基质囊泡中发生的矿化起始过程。