Lys-N is a metalloendopeptidase found in the mushroom Grifola frondosa that cleaves proteins on the amino side of lysine residues.[1]

Crystal structure of Lys-N with co-ordinated zinc atom.[2]

Mass spectrometry

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Lys-N is becoming a popular protease used for protein digestion in proteomics experiments.[citation needed] The combination Lys-N proteolytic peptides and mass spectrometry sequencing with ETD creates tandem mass spectra composed mostly of amino terminal peptide fragment ions.[3] This fragmentation pattern facilitates the applicability of these spectra for de novo peptide sequencing.[3]

See also

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References

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  1. ^ Nonaka T, Hashimoto Y, Takio K (July 1998). "Kinetic characterization of lysine-specific metalloendopeptidases from Grifola frondosa and Pleurotus ostreatus fruiting bodies". Journal of Biochemistry. 124 (1): 157–62. doi:10.1093/oxfordjournals.jbchem.a022074. PMID 9644258.
  2. ^ RCSB Protein Data Bank - RCSB PDB - 1G12 Structure Summary
  3. ^ a b Taouatas N, Drugan MM, Heck AJ, Mohammed S (May 2008). "Straightforward ladder sequencing of peptides using a Lys-N metalloendopeptidase". Nature Methods. 5 (5): 405–7. doi:10.1038/nmeth.1204. PMID 18425140. S2CID 28504546.
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