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Straightforward ladder sequencing of peptides using a Lys-N metalloendopeptidase
Nature Methodsvolume 5, pages405–407 (2008)Cite this article
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Abstract
We introduce a method for sequencing peptides by mass spectrometry using a metalloendopeptidase that cleaves proteins at the amino side of lysine (Lys-N). When analyzed by electron transfer dissociation (ETD)–based mass spectrometric sequencing, Lys-N–digested peptides that contain a single lysine residue produce spectra dominated byc-type fragment ions, providing simple ladders for sequence determination. This method should be a valuable strategy forde novo sequencing and the analysis of post-translational modifications.
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Acknowledgements
We thank A.F.M. Altelaar and B. van Breukelen for fruitful discussions and support. This work was supported by the Netherlands Proteomics Centre.
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Authors and Affiliations
Biomolecular Mass Spectrometry and Proteomics Group, Bijvoet Center for Biomolecular Research and Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Sorbonnelaan 16, Utrecht, 3584 CA, The Netherlands
Nadia Taouatas, Madalina M Drugan, Albert J R Heck & Shabaz Mohammed
- Nadia Taouatas
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- Madalina M Drugan
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- Albert J R Heck
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- Shabaz Mohammed
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Contributions
N.T. and S.M. performed experiments; S.M. and A.J.R.H. designed experiments; N.T., A.J.R.H. and S.M. wrote the paper; M.M.D. analyzed peptide and fragment ion occurences.
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Correspondence toAlbert J R Heck orShabaz Mohammed.
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Supplementary Figures 1–4, Supplementary Tables 1–3, Supplementary Methods (PDF 451 kb)
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Taouatas, N., Drugan, M., Heck, A.et al. Straightforward ladder sequencing of peptides using a Lys-N metalloendopeptidase.Nat Methods5, 405–407 (2008). https://doi.org/10.1038/nmeth.1204
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