Structural proteomics by NMR spectroscopy

Abstract

Structural proteomics is one of the powerful research areas in the postgenomic era, elucidating structure-function relationships of uncharacterized gene products based on the 3D protein structure. It proposes biochemical and cellular functions of unannotated proteins and thereby identifies potential drug design and protein engineering targets. Recently, a number of pioneering groups in structural proteomics research have achieved proof of structural proteomic theory by predicting the 3D structures of hypothetical proteins that successfully identified the biological functions of those proteins. The pioneering groups made use of a number of techniques, including NMR spectroscopy, which has been applied successfully to structural proteomics studies over the past 10 years. In addition, advances in hardware design, data acquisition methods, sample preparation and automation of data analysis have been developed and successfully applied to high-throughput structure determination techniques. These efforts ensure that NMR spectroscopy will become an important methodology for performing structural proteomics research on a genomic scale. NMR-based structural proteomics together with x-ray crystallography will provide a comprehensive structural database to predict the basic biological functions of hypothetical proteins identified by the genome projects.

Cite this paper

@article{shin2008structural,
  title = {{Structural proteomics by NMR spectroscopy}},
  author = {Shin, Joon‐Han and Lee, Woonghee and Lee, Weontae},
  journal = {Expert Review of Proteomics},
  volume = {5},
  number = {4},
  pages = {589--601},
  year = {2008},
  doi = {10.1586/14789450.5.4.589}
}

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