Sayed S. Daoud's Cancer proteomics: from bench to bedside PDF

By Sayed S. Daoud

ISBN-10: 1588298582

ISBN-13: 9781588298584

This booklet covers present subject matters regarding using proteomic options in melanoma remedy in addition to expected demanding situations which could come up from its program in day-by-day perform. It information present applied sciences utilized in proteomics, examines the use proteomics in mobile signaling, offers medical functions of proteomics in melanoma remedy, and appears on the function of the FDA in regulating using proteomics.

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U. S. A. 102:3948–3953, 2005. 100. W. J. Am. Chem. Soc. 124:672–678, 2002. 101. L. Mol. Cell Proteomics 3:872–886, 2004. 102. J. J. Proteome Res. 5:233–239, 2006. 103. A. J. Proteome Res. 5:240–247, 2006. 104. L. Mol. Cell Proteomics 4:1002–1008, 2005. II Cell Signaling Proteomics 2 Integration of Genomics and Proteomics in Dissecting p53 Signaling Kyunghee Lee, Tao Wang, Abdur Rehman, Yuhua Wang, and Sayed S. Daoud CONTENTS 1 Introduction 2 Genomics of p53 Signaling 3 Proteomics and p53 Target Identification 4 Integration of Proteomics in p53 Signaling 5 Conclusions Summary The discovery of the human genome and subsequent expansion of proteomics research combined with emerging technologies such as sophisticated computational biology are producing unprecedented changes in our understanding of the role of tumor suppressors in cell signaling.

This modification also gave an opportunity to add a stable-isotope label (D3 -methyl) for quantitative analyses. This initial report of phosphoproteome analysis described the detection of 216 phosphopeptides and with specific assignment of 383 phosphorylation sites in the yeast proteome (71). In a subsequent set of experiments, this same technique was used in a human system, sperm cells (72). This IMACbased phosphoproteome approach has also been refined to specifically target tyrosine phosphorylation (73,74).

This initial report of phosphoproteome analysis described the detection of 216 phosphopeptides and with specific assignment of 383 phosphorylation sites in the yeast proteome (71). In a subsequent set of experiments, this same technique was used in a human system, sperm cells (72). This IMACbased phosphoproteome approach has also been refined to specifically target tyrosine phosphorylation (73,74). These experiments use anti-phosphotyrosine antibodies to immunopreciptate this sub-class of proteins.

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Cancer proteomics: from bench to bedside by Sayed S. Daoud


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