<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Neef AB</dc:creator>
  <dc:creator>Pernot L</dc:creator>
  <dc:creator>Schreier VN</dc:creator>
  <dc:creator>Scapozza L</dc:creator>
  <dc:creator>Luedtke NW</dc:creator>
  <dc:date>2015</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Pathogen-selective labeling was achieved by using the novel gemcitabine metabolite analogue 2'-deoxy-2',2'-difluoro-5-ethynyluridine (dF-EdU) and click chemistry. Cells infected with Herpes Simplex Virus-1 (HSV-1), but not uninfected cells, exhibit nuclear staining upon the addition of dF-EdU and a fluorescent azide. The incorporation of the dF-EdU into DNA depends on its phosphorylation by a herpes virus thymidine kinase (TK). Crystallographic analyses revealed how dF-EdU is well accommodated in the active site of HSV-1 TK, but steric clashes prevent dF-EdU from binding human TK. These results provide the first example of pathogen-enzyme-dependent incorporation and labeling of bioorthogonal functional groups in human cells.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://sonar.ch/global/documents/3725</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1002/ange.201500250</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/32313318</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:source>Angewandte Chemie (Weinheim an der Bergstrasse, Germany). - 2015</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Bioorthogonale Chemie</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Chemische Reporter</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Klick‐Chemie</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Nukleoside</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Viren</dc:subject>
  <dc:title xmlns:ns6="xml" ns6:lang="en">A Bioorthogonal Chemical Reporter of Viral Infection.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
