<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>Woycechowsky KJ</dc:creator>
  <dc:date>2004</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Directed evolution is a powerful method for generating novel molecules with desirable properties. In developing a new sensor to screen for protein-protein interactions, Tafelmeyer et al. report a clever strategy to evolve heterodimeric "split proteins" from a monomer in this issue of Chemistry &amp; Biology.</dc:description>
  <dc:identifier>https://sonar.ch/global/documents/151904</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1016/j.chembiol.2004.05.005</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/15157869</dc:relation>
  <dc:source>Chemistry &amp; biology. - 2004</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Biosensing Techniques</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Dimerization</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Directed Molecular Evolution</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Gene Library</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Interferon Type I</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Peptide Fragments</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Pregnancy Proteins</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Protein Interaction Mapping</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Proteins</dc:subject>
  <dc:title xmlns:ns10="xml" ns10:lang="en">Recombination of fragmented proteins.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>