4.4 Article

Identification of N-homocysteinylation sites in plasma proteins

期刊

AMINO ACIDS
卷 46, 期 1, 页码 235-244

出版社

SPRINGER WIEN
DOI: 10.1007/s00726-013-1617-7

关键词

Homocysteine thiolactone; Human albumin; Human fibrinogen; N-homocysteinylation; Mass spectrometry

资金

  1. National Science Center, Poland [2011/01/B/NZ1/03417, 2011/02/1/NZ1/00010, 2012/07/B/NZ7/01178, 4306/B/H03/2011/40]

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A protocol for the identification of N-homocysteinylation sites in plasma proteins is described. Human plasma or purified fibrinogen is subjected to trypsin digestion and analysis of N-Hcy-peptides by liquid chromatography/mass spectroscopy (LC/MS). Human fibrinogen is isolated from the plasma by the glycine precipitation method. Identification of N-Hcy-Lys-peptides in tryptic digests of in vivo-derived samples is facilitated by the use of N-Hcy-albumin and N-Hcy-fibrinogen synthesized in vitro from commercially available human proteins. This protocol allows identification of N-homocysteinylation sites at Lys4, Lys12, Lys137, and Lys525 in albumin directly in trypsin-digested human serum samples. N-Hcy-Lys562, N-Hcy-Lys344, and N-Hcy-Lys385 were identified in human fibrinogen from patients with cystathionine beta-synthase deficiency. The protocol can be completed in 4 days.

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