Beernink Hans T H, Nock Steffen
Immunology R&D, BioSource International, 542 Flynn Rd, Camarillo, CA 93012, USA.
Expert Rev Proteomics. 2005 Aug;2(4):487-97. doi: 10.1586/14789450.2.4.487.
Recent advances in analytical methods, particularly in the area of protein microarrays, have brought the field of proteomics to the forefront of biological science. Protein arrays have shown to be useful for the multiplexed analysis of several hundreds of proteins in parallel. While much of the effort has focused on developing methods to identify expressed proteins, the identification of post-translational modifications is equally important for comprehensive proteome characterization. Protein phosphorylation constitutes a major type of post-translational modification that mobilizes a high number of genes, is involved in many crucial cell functions and largely contributes to the complexity of the proteome. One of the major challenges to analyze phosphoproteins using arrays is the availability of specific antibodies. Thus far, this has hampered the development of highly complex phosphoprotein arrays. This review discusses some of the recent progress made in the development of techniques and reagents to quantitatively determine sites of protein phosphorylation.
分析方法的最新进展,特别是在蛋白质微阵列领域,已将蛋白质组学领域推向生物科学的前沿。蛋白质阵列已被证明可用于同时对数百种蛋白质进行多重分析。虽然大部分努力都集中在开发鉴定表达蛋白质的方法上,但翻译后修饰的鉴定对于全面的蛋白质组表征同样重要。蛋白质磷酸化是翻译后修饰的一种主要类型,它调控大量基因,参与许多关键的细胞功能,并在很大程度上导致了蛋白质组的复杂性。使用阵列分析磷酸化蛋白质的主要挑战之一是特异性抗体的可用性。到目前为止,这阻碍了高度复杂的磷酸化蛋白质阵列的发展。本文综述了在开发定量测定蛋白质磷酸化位点的技术和试剂方面取得的一些最新进展。