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Langmuir ; 31(25): 7148-57, 2015 Jun 30.
Artigo em Inglês | MEDLINE | ID: mdl-26048139

RESUMO

Impedimetric lectin biosensors capable of recognizing two different carbohydrates (galactose and sialic acid) in glycans attached to antibodies isolated from human serum were prepared. The first step entailed the modification of a gold surface by a self-assembled monolayer (SAM) deposited from a solution containing a carboxybetaine-terminated thiol applied to the subsequent covalent immobilization of lectins and to resist nonspecific protein adsorption. In the next step, Sambucus nigra agglutinin (SNA) or Ricinus communis agglutinin (RCA) was covalently attached to the SAM, and the whole process of building a bioreceptive layer was optimized and characterized using a diverse range of techniques including electrochemical impedance spectroscopy, cyclic voltammetry, quartz crystal microbalance, contact angle measurements, zeta-potential assays, X-ray photoelectron spectroscopy, and atomic force microscopy. In addition, the application of the SNA-based lectin biosensor in the glycoprofiling of antibodies isolated from the human sera of healthy individuals and of patients suffering from rheumatoid arthritis (RA) was successfully validated using an SNA-based lectin microarray. The results showed that the SNA lectin, in particular, is capable of discriminating between the antibodies isolated from healthy individuals and those from RA patients based on changes in the amount of sialic acid present in the antibodies. In addition, the results obtained by the application of RCA and SNA biosensors indicate that the abundance of galactose and sialic acid in antibodies isolated from healthy individuals is age-related.


Assuntos
Betaína/química , Técnicas Biossensoriais/métodos , Galactose/análise , Imunoglobulina G/sangue , Imunoglobulina G/química , Ácido N-Acetilneuramínico/análise , Compostos de Sulfidrila/química , Artrite Reumatoide/sangue , Betaína/análogos & derivados , Eletroquímica , Humanos , Modelos Moleculares , Lectinas de Plantas/química , Conformação Proteica
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