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Synthesis of redox-active fluorinated 5-hydroxytryptophans as molecular reporters for biological electron transfer.
Ohler, Amanda; Long, Hanna; Ohgo, Kei; Tyson, Kristin; Murray, David; Davis, Amanda; Whittington, Chris; Hvastkovs, Eli G; Duffy, Liam; Haddy, Alice; Sargent, Andrew L; Allen, William E; Offenbacher, Adam R.
Affiliation
  • Ohler A; Department of Chemistry, East Carolina University, Greenville, NC, USA. offenbachera17@ecu.edu.
Chem Commun (Camb) ; 57(25): 3107-3110, 2021 Mar 28.
Article in En | MEDLINE | ID: mdl-33626126
ABSTRACT
Fluorinated 5-hydroxytryptophans (Fn-5HOWs) were synthesized in gram scale quantities and incorporated into a ß-hairpin peptide and the protein azurin. The redox-active Fn-5HOWs exhibit unique radical spectroscopic signatures that expand the function of as probes for biological electron transfer.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: 5-Hydroxytryptophan / Halogenation Language: En Journal: Chem Commun (Camb) Journal subject: QUIMICA Year: 2021 Document type: Article Affiliation country: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: 5-Hydroxytryptophan / Halogenation Language: En Journal: Chem Commun (Camb) Journal subject: QUIMICA Year: 2021 Document type: Article Affiliation country: United States