<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>Labouesse, Marie A.</dc:creator>
  <dc:creator>Cola, Reto B.</dc:creator>
  <dc:creator>Patriarchi, Tommaso</dc:creator>
  <dc:date>2020-10-28</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Understanding how dopamine (DA) encodes behavior depends on technologies that  can reliably monitor DA release in freely-behaving animals. Recently, red and green  genetically encoded sensors for DA (dLight, GRAB-DA) were developed and now  provide the ability to track release dynamics at a subsecond resolution, with  submicromolar affinity and high molecular specificity. Combined with rapid  developments in in vivo imaging, these sensors have the potential to transform the  field of DA sensing and DA-based drug discovery. When implementing these tools in  the laboratory, it is important to consider there is not a ‘one-size-fits-all’ sensor. Sensor  properties, most importantly their affinity and dynamic range, must be carefully chosen  to match local DA levels. Molecular specificity, sensor kinetics, spectral properties,  brightness, sensor scaffold and pharmacology can further influence sensor choice  depending on the experimental question. In this review, we use DA as an example; we  briefly summarize old and new techniques to monitor DA release, including DA  biosensors. We then outline a map of DA heterogeneity across the brain and provide  a guide for optimal sensor choice and implementation based on local DA levels and  other experimental parameters. Altogether this review should act as a tool to guide DA  sensor choice for end-users.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/308979</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/308979/files/col_gbd.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.3390/ijms21218048</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>International Journal of Molecular Sciences. - 2020, vol. 21, no. 21, p. 8048</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">GPCR-based dopamine sensors—a detailed guide to inform sensor choice for in vivo imaging</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
