Analysis of yeast protein kinases using protein chips
Top Cited Papers
- 1 November 2000
- journal article
- research article
- Published by Springer Nature in Nature Genetics
- Vol. 26 (3) , 283-289
- https://doi.org/10.1038/81576
Abstract
We have developed a novel protein chip technology that allows the high-throughput analysis of biochemical activities, and used this approach to analyse nearly all of the protein kinases from Saccharomyces cerevisiae. Protein chips are disposable arrays of microwells in silicone elastomer sheets placed on top of microscope slides. The high density and small size of the wells allows for high-throughput batch processing and simultaneous analysis of many individual samples. Only small amounts of protein are required. Of 122 known and predicted yeast protein kinases, 119 were overexpressed and analysed using 17 different substrates and protein chips. We found many novel activities and that a large number of protein kinases are capable of phosphorylating tyrosine. The tyrosine phosphorylating enzymes often share common amino acid residues that lie near the catalytic region. Thus, our study identified a number of novel features of protein kinases and demonstrates that protein chip technology is useful for high-throughput screening of protein biochemical activity.Keywords
This publication has 40 references indexed in Scilit:
- Using Elastomeric Membranes as Dry Resists and for Dry Lift-OffLangmuir, 1999
- Exploring the Metabolic and Genetic Control of Gene Expression on a Genomic ScaleScience, 1997
- SBF Cell Cycle Regulator as a Target of the Yeast PKC-MAP Kinase PathwayScience, 1997
- The protein kinases of budding yeast: six score and moreTrends in Biochemical Sciences, 1997
- Life with 6000 GenesScience, 1996
- Selection of axial growth sites in yeast requires Axl2p, a novel plasma membrane glycoprotein.Genes & Development, 1996
- A highly divergent gamma-tubulin gene is essential for cell growth and proper microtubule organization in Saccharomyces cerevisiae.The Journal of cell biology, 1995
- Two structures of the catalytic domain of phosphorylase kinase: an active protein kinase complexed with substrate analogue and productStructure, 1995
- Rapid and Sensitive Protein Similarity SearchesScience, 1985
- Construction of Phylogenetic TreesScience, 1967