Posttranslational modifications in human plasma MBL and human recombinant MBL

Pia Hønnerup Jensen, Inga Laursen, Finn Matthiesen, Peter Højrup

Research output: Contribution to journalJournal articleResearchpeer-review


Mannan-binding lectin (MBL) is a complex serum protein that plays an important role in innate immunity. In addition to assuming several different oligomeric forms, the polypeptide itself is highly heterogeneous. This heterogeneity is due to post-translational modifications, which help to stabilize the intact protein in its active conformation. For the first time, positions and occupation frequency of partial hydroxylations and partial glycosylations are reported in MBL. Hydroxylation and glycosylation patterns of both recombinant and plasma derived MBL were determined, using a combination of mass spectrometry on reduced MBL and on enzyme cleaved MBL. Variations in the degree of hydroxylation and glycosylation seem to be an indigenous characteristic of collectins. In addition to these already known modifications, a new post-translational modification was identified. Cys(216) (and occasionally also Cys(202)) was modified in trace amounts to dehydroalanine, as detected by a 34 Da mass loss. This impairs the formation of a disulphide bond in the carbohydrate recognition domain. The dehydroalanine was identified in similar small amounts in both recombinant and plasma-derived MBL.
Original languageEnglish
JournalBBA General Subjects
Issue number3
Pages (from-to)335-344
Number of pages9
Publication statusPublished - 1. Mar 2007



  • Amino Acid Sequence
  • Amino Acids
  • Chromatography, High Pressure Liquid
  • Glycosylation
  • Humans
  • Hydroxylation
  • Mannose-Binding Lectin
  • Molecular Sequence Data
  • Peptides
  • Protein Processing, Post-Translational
  • Recombinant Proteins
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization

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