Abstract
Dip-pen nanolithography was used to construct arrays of proteins with 100- to 350-nanometer features. These nanoarrays exhibit almost no detectable nonspecific binding of proteins to their passivated portions even in complex mixtures of proteins, and therefore provide the opportunity to study a variety of surface-mediated biological recognition processes. For example, reactions involving the protein features and antigens in complex solutions can be screened easily by atomic force microscopy. As further proof-of-concept, these arrays were used to study cellular adhesion at the submicrometer scale.
MeSH terms
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3T3 Cells
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Adsorption
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Animals
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Cell Adhesion
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Fibronectins* / chemistry
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Fibronectins* / metabolism
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Focal Adhesions
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Immunoglobulin G* / chemistry
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Immunoglobulin G* / metabolism
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Mice
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Microscopy, Atomic Force
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Miniaturization
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Muramidase* / chemistry
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Muramidase* / metabolism
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Nanotechnology*
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Palmitic Acids / chemistry*
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Protein Binding
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Proteins* / chemistry
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Proteins* / metabolism
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Receptor Aggregation
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Recombinant Proteins / chemistry
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Recombinant Proteins / metabolism
Substances
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16-mercaptohexadecanoic acid
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Fibronectins
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Immunoglobulin G
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Palmitic Acids
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Proteins
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Recombinant Proteins
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Muramidase