<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>Zhao, Huiyuan</dc:creator>
  <dc:creator>Huang, Shuai</dc:creator>
  <dc:creator>Palanisamy, Sivakumar</dc:creator>
  <dc:creator>Wang, Cui</dc:creator>
  <dc:creator>Rainer, Gregor</dc:creator>
  <dc:creator>Zhang, Xiaozhe</dc:creator>
  <dc:date>2020-06-15</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Alpha‐synuclein (α‐syn) dopaminylation can lead to the death of dopaminergic  neurons in the brain and is a risk factor of Parkinson's  disease (PD). This study aims to examine whether such a posttranslational  modification (PTM) is presented in human blood plasma. Experimental Design: In vitro reaction simulation between α‐syn and dopamine (DA) is  conducted to study the biochemical mechanism.  Then α‐syn from human blood plasma samples is detected by using  immunoprecipitation‐mass spectrometry (IP‐MS). Lastly the levels of  endogenous α‐syn and α‐syn dopaminylation in 88 blood plasma samples from  patients with PD, major depressive disorder (MDD), and  healthy control (HC) are compared. Results: DA modifies α‐syn with the addition of dopamine‐quinone (DAQ) into lysine  sites of α‐syn in vitro and the addition of DAQ and  3,4‐dihydroxyphenylacetaldehyde (DOPAL) in plasma samples. The unmodified α‐syn  between the PD and HC groups showed similar  levels. The levels of two peptides, one with lysine 34 (34K) DAQ modification and the  other with lysine 23 (23K) ubiquitination, are  significantly higher in PD and MDD compared with HC. Conclusions and Clinical Relevance: Thus, α‐syn dopaminylation is measurable and  might be used to indicatethe presence and  progression of neurological disorders.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/308989</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/308989/files/rai_asd.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/308989/files/rai_asd_sm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1002/prca.201900117</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>PROTEOMICS – Clinical Applications. - 2020, vol. 14, no. 5, p. 1900117</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Alpha‐synuclein dopaminylation presented in plasma of both healthy subjects and parkinson’s disease patients</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
