Rungsihirunrat Kanchana, Chaijaroenkul Wanna, Siripoon Napaporn, Seugorn Aree, Thaithong Sodsri, Na-Bangchang Kesara
College of Public Health Sciences, Chulalongkorn University, Bangkok 10330, Thailand.
Asian Pac J Trop Biomed. 2012 Jan;2(1):66-9. doi: 10.1016/S2221-1691(11)60192-5.
To compare the protein patterns from the extracts of the mutant clone T9/94-M1-1(b3) induced by pyrimethamine, and the original parent clone T9/94 following separation of parasite extracts by two-dimensional electrophoresis (2-DE).
Proteins were solubilized and separated according to their charges and sizes. The separated protein spots were then detected by silver staining and analyzed for protein density by the powerful image analysis software.
Differentially expressed protein patterns (up- or down-regulation) were separated from the extracts from the two clones. A total of 223 and 134 protein spots were detected from the extracts of T9/94 and T9/94-M1-1(b3) clones, respectively. Marked reduction in density of protein expression was observed with the extract from the mutant (resistant) clone compared with the parent (sensitive) clone. A total of 25 protein spots showed at least two-fold difference in density, some of which exhibited as high as ten-fold difference.
These proteins may be the molecular targets of resistance of Plasmodium falciparum to pyrimethamine. Further study to identify the chemical structures of these proteins by mass spectrometry is required.
通过二维电泳(2-DE)分离疟原虫提取物后,比较乙胺嘧啶诱导的突变克隆T9/94-M1-1(b3)与原始亲本克隆T9/94提取物的蛋白质图谱。
根据蛋白质的电荷和大小进行溶解和分离。然后通过银染检测分离出的蛋白质斑点,并使用强大的图像分析软件分析蛋白质密度。
从两个克隆的提取物中分离出差异表达的蛋白质图谱(上调或下调)。分别从T9/94和T9/94-M1-1(b3)克隆的提取物中检测到总共223个和134个蛋白质斑点。与亲本(敏感)克隆相比,突变(抗性)克隆的提取物中观察到蛋白质表达密度明显降低。共有25个蛋白质斑点的密度显示至少两倍的差异,其中一些差异高达十倍。
这些蛋白质可能是恶性疟原虫对乙胺嘧啶耐药的分子靶点。需要进一步研究通过质谱鉴定这些蛋白质的化学结构。