A study of polyethylene glycol backfilling for enhancing target recognition using QCM-D and DPI. Issue 39 (21st September 2018)

• Record Type: Journal Article
• Authors: Du, Yanqiu; Jin, Jing; Jiang, Wei
• Is Part Of: Journal of materials chemistry. Volume 6:Issue 39(2018)
• Page Start: 6217
• Page End: 6224
• Publication Date: 2018-09-21
• Subjects: Materials -- Periodicals; Chemistry, Analytic -- Periodicals; Biomedical materials -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c8tb01526k
• Languages: English
• ISSNs: 2050-750X

Abstract

Abstract : Long PEGs were used to bind biomolecules and short PEGs were used to backfill and suppress nonspecific protein adsorption. Abstract : Polyethylene glycol (PEG) is a promising candidate for protein resistance and preserving protein function in biomedical applications. In this study, a PEG-based bifunctional platform with antifouling for plasma proteins and high sensitivity for biomolecules was designed. Long PEG chains (PEG24 ) were used to install functional biomolecules, and short PEG chains (PEG4 ) served as a protective layer to backfill the surface and suppress nonspecific protein adsorption. Quartz crystal microbalance with dissipation (QCM-D) and dual polarization interferometry (DPI) were combined to investigate the dynamic process of PEG4 backfilling and the recognition capacity of biomolecules with different ratios of PEG4 and PEG24 in real time. The amount of PEG4 chain backfilling affected the flexibility of PEG24 and exposed sites. The recognition capacity was improved by increasing the ratios of PEG4 to PEG24 . Therefore, when the feeding ratio of PEG4 to PEG24 was 9 : 1, a highly efficient and sensitive platform was constructed for immobilization of antibodies and recognition of antigens either in pure PBS or in a complex biological environment.