Take a sneak peek at the new NIST.gov and let us know what you think!
(Please note: some content may not be complete on the beta site.).
NIST Authors in Bold
|Author(s):||Germarie Sanchez-Pomales; Todd A. Morris; James Falabella; Michael J. Tarlov; Rebecca A. Zangmeister;|
|Title:||A Lectin-Based Gold Nanoparticle Assay for Probing Glycosylation of Glycoproteins|
|Published:||April 17, 2012|
|Abstract:||We report a glycoanalysis method in which lectins are used to probe the glycans of glycoproteins that are adsorbed on gold nanoparticles. A model mannose-presenting glycoprotein, ribonuclease B (RNase B), and the therapeutic monoclonal antibody (mAb) Rituxan®, were found to adsorb spontaneously and non-specifically to bare gold nanoparticles such that glycans were accessible for lectin binding. Addition of a multivalent binding lectin, such as concanavalin A (Con A), to a solution of the modified gold nanoparticles resulted in cross-linking of the nanoparticles. This phenomenon was evidenced within 1 minute by a change in the hydrodynamic radius, DH, measured by dynamic light scattering (DLS) and a shift and increase in absorbance of the plasmon resonance band of the gold nanoparticles. By combining the sugar-binding specificity and the cross-linking capabilities of lectins, the non-specific adsorption of glycoproteins to gold surfaces, and the unique optical reporting properties of gold nanoparticles, a glycosylation pattern of RNase B and Rituxan® could be generated. This assay provides advantages over currently used glycoanalysis methods in terms of short analysis time, simplicity of the conjugation method, convenience of simple spectroscopic detection, and feasibility of providing glycan characterization of the protein drug product by using a variety of binding lectins.|
|Citation:||Biotechnology and Bioengineering|
|Pages:||pp. 2240 - 2249|
|Keywords:||glycoprotein, glycan, assay, antibody, lectin, gold nanoparticle|
|Research Areas:||Nanobiotechnology, Biological Product Characterization, Drugs/Pharmaceuticals|
|DOI:||http://dx.doi.org/10.1002/bit.24513 (Note: May link to a non-U.S. Government webpage)|
|PDF version:||Click here to retrieve PDF version of paper (963KB)|