TY - JOUR
T1 - A quantitative peptide array for evaluation of protein kinase activity
AU - Han, Xiaoming
AU - Shigaki, Syuhei
AU - Yamaji, Takayuki
AU - Yamanouchi, Go
AU - Mori, Takeshi
AU - Niidome, Takuro
AU - Katayama, Yoshiki
N1 - Funding Information:
This work was supported by New Energy and Industrial Technology Development Organization (NEDO) and CREST, Japan Science and Technology (JST).
PY - 2008/1/1
Y1 - 2008/1/1
N2 - Peptide array, which is known as an emerging technology, has been developed for identification of protein kinase activity. For this purpose, the ability of quantitative analysis is very important because the absolute change in protein kinase activity is critical for the determination of cellular function. Here we report an original type of peptide array for quantitative evaluation of protein kinase activity by fluorescence imaging. We used the peptide array for the quantitative evaluation of the nonreceptor tyrosine kinase c-Src activity as a model for detecting protein kinase activities. By using positive and negative control peptides, we obtained the actual ratio of tyrosine phosphorylation of substrate peptide not only by purified c-Src but also by c-Src in cell lysate. In addition, the experimental approach provided simple immobilization of peptide. Our sensitive, specific, and high-throughput peptide array can be used for quantitative evaluation of kinase activity and potentially can be applied to drug discovery and screening.
AB - Peptide array, which is known as an emerging technology, has been developed for identification of protein kinase activity. For this purpose, the ability of quantitative analysis is very important because the absolute change in protein kinase activity is critical for the determination of cellular function. Here we report an original type of peptide array for quantitative evaluation of protein kinase activity by fluorescence imaging. We used the peptide array for the quantitative evaluation of the nonreceptor tyrosine kinase c-Src activity as a model for detecting protein kinase activities. By using positive and negative control peptides, we obtained the actual ratio of tyrosine phosphorylation of substrate peptide not only by purified c-Src but also by c-Src in cell lysate. In addition, the experimental approach provided simple immobilization of peptide. Our sensitive, specific, and high-throughput peptide array can be used for quantitative evaluation of kinase activity and potentially can be applied to drug discovery and screening.
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U2 - 10.1016/j.ab.2007.09.026
DO - 10.1016/j.ab.2007.09.026
M3 - Article
C2 - 18028866
AN - SCOPUS:36048954230
SN - 0003-2697
VL - 372
SP - 106
EP - 115
JO - Analytical Biochemistry
JF - Analytical Biochemistry
IS - 1
ER -