Baker Scott E, Panisko Ellen A
Pacific Northwest National Laboratory, Richland, WA, USA.
Methods Mol Biol. 2011;722:133-9. doi: 10.1007/978-1-61779-040-9_9.
The continued fast pace of fungal genome sequence generation has enabled proteomic analysis of a wide variety of organisms that span the breadth of the Kingdom Fungi. There is some phylogenetic bias to the current catalog of fungi with reasonable DNA sequence databases (genomic or EST) that could be analyzed at a global proteomic level. However, the rapid development of next generation sequencing platforms has lowered the cost of genome sequencing such that in the near future, having a genome sequence will no longer be a time or cost bottleneck for downstream proteomic (and transcriptomic) analyses. High throughput, nongel-based proteomics offers a snapshot of proteins present in a given sample at a single point in time. There are a number of variations on the general methods and technologies for identifying peptides in a given sample. We present a method that can serve as a "baseline" for proteomic studies of fungi.
真菌基因组序列生成的持续快速发展,使得对涵盖真菌界广度的各种生物体进行蛋白质组分析成为可能。目前具有合理DNA序列数据库(基因组或EST)且可在全球蛋白质组水平进行分析的真菌目录存在一些系统发育偏差。然而,新一代测序平台的快速发展降低了基因组测序成本,以至于在不久的将来,拥有基因组序列将不再是下游蛋白质组(和转录组)分析的时间或成本瓶颈。高通量、非基于凝胶的蛋白质组学可在单个时间点提供给定样品中存在的蛋白质的快照。在给定样品中鉴定肽段的一般方法和技术有多种变体。我们提出了一种可作为真菌蛋白质组学研究“基线”的方法。