Szczepaniak Joanna, Łukaszewicz Marcin, Krasowska Anna
Faculty of Biotechnology, University of Wroclaw Wroclaw, Poland.
Front Microbiol. 2015 Dec 9;6:1382. doi: 10.3389/fmicb.2015.01382. eCollection 2015.
We present a fluorometric method for determining ABC transporter activity in the pathogenic fungus C. albicans during different growth phases and in response to glucose. The carbocyanine dye diS-C3(3) was previously used to monitor plasma membrane potentials and test the influence of surface-active compounds in membrane polarization. We used diS-C3(3) to show changes in fluorescence kinetics that reflect changes in the activity of ABC transporters in C. albicans growth. Cdr1-GFP fluorescence, revealed that Cdr1p relocates to the inside of the cell after the early-log growth phase. Addition of glucose to the cell suspension resulted in Cdr1p transporter expression in the CDR2-knockout strain. We confirmed the diS-C3(3) results by standard RT-PCR and Western blotting.
我们提出了一种荧光测定方法,用于确定致病真菌白色念珠菌在不同生长阶段以及对葡萄糖响应时ABC转运蛋白的活性。碳菁染料diS-C3(3) 此前被用于监测质膜电位,并测试表面活性化合物对膜极化的影响。我们使用diS-C3(3) 来显示荧光动力学的变化,这些变化反映了白色念珠菌生长过程中ABC转运蛋白活性的变化。Cdr1-GFP荧光显示,在对数生长早期阶段后,Cdr1p重新定位到细胞内部。向细胞悬液中添加葡萄糖会导致CDR2基因敲除菌株中Cdr1p转运蛋白的表达。我们通过标准RT-PCR和蛋白质免疫印迹法证实了diS-C3(3) 的实验结果。