The Centre for Bioinformatics, Department of Life Sciences, Imperial College, London SW7 2AZ.
Parasitology. 2012 Aug;139(9):1131-45. doi: 10.1017/S0031182012000133. Epub 2012 Feb 16.
Here we discuss proteomic analyses of whole cell preparations of the mosquito stages of malaria parasite development (i.e. gametocytes, microgamete, ookinete, oocyst and sporozoite) of Plasmodium berghei. We also include critiques of the proteomes of two cell fractions from the purified ookinete, namely the micronemes and cell surface. Whereas we summarise key biological interpretations of the data, we also try to identify key methodological constraints we have met, only some of which we were able to resolve. Recognising the need to translate the potential of current genome sequencing into functional understanding, we report our efforts to develop more powerful combinations of methods for the in silico prediction of protein function and location. We have applied this analysis to the proteome of the male gamete, a cell whose very simple structural organisation facilitated interpretation of data. Some of the in silico predictions made have now been supported by ongoing protein tagging and genetic knockout studies. We hope this discussion may assist future studies.
在这里,我们讨论了疟原虫发育的蚊期(即配子体、小配子、动合子、卵囊和子孢子)的全细胞制剂的蛋白质组学分析。我们还包括对纯化的动合子的两个细胞部分(微线体和细胞表面)的蛋白质组的批评。虽然我们总结了数据的关键生物学解释,但我们也试图确定我们遇到的关键方法学限制,其中只有一些我们能够解决。认识到需要将当前基因组测序的潜力转化为功能理解,我们报告了我们为开发更强大的方法组合以进行蛋白质功能和位置的计算机预测所做的努力。我们已经将这种分析应用于雄性配子体的蛋白质组,该细胞的结构组织非常简单,便于解释数据。现在,一些计算机预测已经得到了正在进行的蛋白质标记和遗传敲除研究的支持。我们希望本次讨论能为未来的研究提供帮助。