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Protein attachment to silane-functionalized porous silicon: A comparison of electrostatic and covalent attachment.

Published on Aug 1, 2015in Journal of Colloid and Interface Science6.361
· DOI :10.1016/j.jcis.2015.04.022
Malgorzata Baranowska4
Estimated H-index: 4
,
Agata J. Slota2
Estimated H-index: 2
+ 5 AuthorsLluis F. Marsal32
Estimated H-index: 32
Abstract
Abstract Porous silicon (pSi) is a prosperous biomaterial, biocompatible, and biodegradable. Obtaining regularly functionalized pSi surfaces is required in many biotechnology applications. Silane–PEG–NHS (triethoxysilane–polyethylene-glycol–N-hydroxysuccinimide) is useful for single-molecule studies due to its ability to attach to only one biomolecule. We investigate the functionalization of pSi with silane–PEG–NHS and compare it with two common grafting agents: APTMS (3-aminopropylotrimethoxysilane) as electrostatic linker, and APTMS modified with glutaraldehyde as covalent spacer. We show the arrangement of two proteins (collagen and bovine serum albumin) as a function of the functionalization and of the pore size. FTIR is used to demonstrate correct functionalization while fluorescence confocal microscopy reveals that silane–PEG–NHS results in a more uniform protein distribution. Reflection interference spectroscopy (RIfS) is used to estimate the attachment of linker and proteins. The results open a way to obtain homogenous chemical modified silicon supports with a great value in biosensing, drug delivery and cell biology.
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