Abstract
Caged aptamers represent valuable tools for the spatiotemporal control of protein function by light. Here we describe a general route starting with the de novo selection process targeting cytohesin-1 and aiming at the synthesis of caged aptamers without the prior knowledge of detailed structural determinants of aptamer-target binding.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Aptamers, Nucleotide / chemical synthesis
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Aptamers, Nucleotide / chemistry
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Aptamers, Nucleotide / pharmacology*
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Base Sequence
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Binding Sites
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DNA, Single-Stranded / chemical synthesis
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DNA, Single-Stranded / chemistry
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DNA, Single-Stranded / pharmacology*
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Guanine Nucleotide Exchange Factors / antagonists & inhibitors*
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Guanine Nucleotide Exchange Factors / chemistry
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Light*
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Molecular Sequence Data
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Structure-Activity Relationship
Substances
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Aptamers, Nucleotide
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DNA, Single-Stranded
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Guanine Nucleotide Exchange Factors
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cytohesin-1