Shotgun proteomics
From Wikipedia, the free encyclopedia
Shotgun proteomics is a method of identifying proteins in complex mixtures using a combination of high performance liquid chromatography combined with mass spectrometry.[1][2][3] The name is derived from shotgun sequencing of DNA which is itself named by analogy with the rapidly-expanding, quasi-random firing pattern of a shotgun. In shotgun proteomics, the proteins in the mixture are digested and the resulting peptides are separated by liquid chromatography. Tandem mass spectrometry is then used to identify the peptides.
[edit] See also
[edit] References
- ^ Hu L, Ye M, Jiang X, Feng S, Zou H (2007). "Advances in hyphenated analytical techniques for shotgun proteome and peptidome analysis--a review". Anal. Chim. Acta 598 (2): 193–204. doi: . PMID 17719892.
- ^ Fournier ML, Gilmore JM, Martin-Brown SA, Washburn MP (2007). "Multidimensional separations-based shotgun proteomics". Chem. Rev. 107 (8): 3654–86. doi: . PMID 17649983.
- ^ Nesvizhskii AI (2007). "Protein identification by tandem mass spectrometry and sequence database searching". Methods Mol. Biol. 367: 87–119. doi: . PMID 17185772.
[edit] Bibliography
- Marcotte EM (2007). "How do shotgun proteomics algorithms identify proteins?". Nat. Biotechnol. 25 (7): 755–7. doi: . PMID 17621303.
- Yates, John W.; Veenstra, Timothy D.. Proteomics for Biological Discovery. New York: Wiley-Liss. ISBN 0-471-16005-9.