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Efficacy of glycoprotein enrichment by microscale lectin affinity chromatography

✍ Scribed by Milan Madera; Benjamin Mann; Yehia Mechref; Milos V. Novotny


Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
921 KB
Volume
31
Category
Article
ISSN
1615-9306

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✦ Synopsis


Abstract

Reproducible and efficient affinity enrichment is increasingly viewed as an essential step in many investigations leading to the discovery of new biomarkers. In this work, we have evaluated the repeatability of lectin enrichment of glycoproteins from human blood serum through both qualitative and quantitative proteomic approaches. In a comprehensive evaluation of lectin binding, we have performed 30 separate microscale lectin affinity chromatography experiments, followed by a conventional sample purification, and LC‐MS/MS analysis of the enriched glycoproteins. Two lectin affinity matrixes, both with Con A lectin, immobilized to the same solid support but differing in the amount of immobilized lectin, were investigated to characterize their binding properties. Both qualitative and quantitative data indicate acceptable repeatability and binding efficiency for the lectin materials received from two different commercial sources.


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Enrichment of yeast protein tyrosine kin
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The direct biochemical analysis of protein tyrosine kinases from yeast has been difficult due to their very low activity in crude cell lysates. Here we present a procedure for the enrichment and partial purification of protein tyrosine kinases from Saccharomyces cerevisiae based on single-step subst