Fintan steele biography template
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Significance
Aptamers are now used ubiquitously as binding agents for a broad range of applications. Natural (unmodified) DNA and RNA aptamers have considerably less chemical diversity than protein-based ligands such as antibodies, limiting their utility. Aptamers possessing a single chemical modification have helped bridge this diversity gap. We report the selection and identification of aptamers with two diversity-enhancing chemical modifications that bind and inhibit proprotein convertase subtilisin/kexin type 9 (PCSK9), a representative human therapeutic protein target. The addition of a second modification, especially in certain pairwise combinations, resulted in significant improvements in affinity, ligand efficiency, epitope coverage, metabolic stability, and inhibitory activity. Extensively chemically functionalized aptamers have the potential to become the next generation of nucleic-acid–based ligands.
Keywords: SELEX, modified aptamer, PCSK9, SOMAmer, PSMA
Abstract
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US6204248B1 - Pharmaceutical preparations of glutathione and methods of administration thereof - Google Patents
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- US6204248B1 US6204248B1US09/457,642US45764299AUS6204248B1US 6204248 B1US6204248 B1US 6204248B1US 45764299 AUS45764299 AUS 45764299AUS 6204248 B1US6204248 B1US 6204248B1
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- glutathione
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