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        <datestamp>2026-10-01T17:28:26Z</datestamp>
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          <dc:title>&lt;p&gt;AlphaFold prediction and cellular validation of the interaction between TET2 and Vpr.&lt;/p&gt;</dc:title>
          <dc:creator>Dianhong Wang (25157696)</dc:creator>
          <dc:creator>Weijia Ding (554415)</dc:creator>
          <dc:creator>Jingwei Xu (337549)</dc:creator>
          <dc:creator>Ruofan Li (1568194)</dc:creator>
          <dc:creator>Tamino Cairoli (25157699)</dc:creator>
          <dc:creator>Qi Liu (33068)</dc:creator>
          <dc:creator>Yiying Zhu (8675928)</dc:creator>
          <dc:creator>Ye Xiang (522776)</dc:creator>
          <dc:subject>Biophysics</dc:subject>
          <dc:subject>Biochemistry</dc:subject>
          <dc:subject>Cell Biology</dc:subject>
          <dc:subject>Evolutionary Biology</dc:subject>
          <dc:subject>Infectious Diseases</dc:subject>
          <dc:subject>Plant Biology</dc:subject>
          <dc:subject>Virology</dc:subject>
          <dc:subject>various restriction factors</dc:subject>
          <dc:subject>ring e3 ligase</dc:subject>
          <dc:subject>larger tet2 fragment</dc:subject>
          <dc:subject>findings could facilitate</dc:subject>
          <dc:subject>diverse substrate recruitment</dc:subject>
          <dc:subject>vprbp could enable</dc:subject>
          <dc:subject>vprbp adopt either</dc:subject>
          <dc:subject>xlink "&gt; hiv</dc:subject>
          <dc:subject>two &amp;# 8220</dc:subject>
          <dc:subject>recruits diverse substrates</dc:subject>
          <dc:subject>bound host factors</dc:subject>
          <dc:subject>like domains adopt</dc:subject>
          <dc:subject>diverse vpr</dc:subject>
          <dc:subject>host cul4</dc:subject>
          <dc:subject>&amp;# 8220</dc:subject>
          <dc:subject>vprbp mediates</dc:subject>
          <dc:subject>vprbp dimerization</dc:subject>
          <dc:subject>receptor vprbp</dc:subject>
          <dc:subject>&amp;# 8221</dc:subject>
          <dc:subject>structures highlight</dc:subject>
          <dc:subject>structural basis</dc:subject>
          <dc:subject>results pinpoint</dc:subject>
          <dc:subject>molecular architecture</dc:subject>
          <dc:subject>may assist</dc:subject>
          <dc:subject>lish domain</dc:subject>
          <dc:subject>key protein</dc:subject>
          <dc:subject>guided development</dc:subject>
          <dc:subject>divergent stoichiometries</dc:subject>
          <dc:subject>directly interact</dc:subject>
          <dc:subject>different vpr</dc:subject>
          <dc:subject>conformational dynamics</dc:subject>
          <dc:subject>accommodating vpr</dc:subject>
          <dc:subject>1 vpr</dc:subject>
          <dc:subject>1 hijacks</dc:subject>
          <dc:description>&lt;p&gt;&lt;b&gt;(A)&lt;/b&gt; AlphaFold prediction of the Vpr-TET2 interaction. Residues involved in the interactions are shown as sticks. &lt;b&gt;(B)&lt;/b&gt; Western blot analysis of TET2 co-transfected with Vpr or Vpr mutants in HEK293T cells. β-actin was used as an internal loading control. Vpr mutant Q65R, which is deficient in VprBP binding, was used as a negative control. (&lt;b&gt;C&lt;/b&gt;) Statistical quantification of biological replicates. Densitometric quantification derived from the three independent experimental repeats. Data are presented as mean. Error bars represent the standard deviation (SD). &lt;i&gt;n.s.&lt;/i&gt;, not statistically significant (&lt;i&gt;P&lt;/i&gt; &gt; 0.05); *, &lt;i&gt;P&lt;/i&gt; &lt; 0.05. (&lt;b&gt;D&lt;/b&gt;) Functional validation of the Vpr C-terminal mutant in TET2 degradation. Western blot analysis showing that the Vpr C-terminal R88A mutant maintains its capacity to degrade TET2. Western blots were performed in three independent biological replicates (&lt;i&gt;n&lt;/i&gt; = 3) with one representative blot shown. (&lt;b&gt;E&lt;/b&gt;) Statistical quantification of biological replicates. Densitometric quantification derived from the three independent experimental repeats. Data are presented as mean. Error bars represent the standard deviation (SD). &lt;i&gt;n.s.&lt;/i&gt;, not statistically significant (&lt;i&gt;P&lt;/i&gt; &gt; 0.05); *, &lt;i&gt;P&lt;/i&gt; &lt; 0.05; ***, &lt;i&gt;P&lt;/i&gt; &lt; 0.001.&lt;/p&gt; &lt;p&gt;(TIF)&lt;/p&gt;</dc:description>
          <dc:date>2026-10-01T17:28:02Z</dc:date>
          <dc:type>Image</dc:type>
          <dc:type>Figure</dc:type>
          <dc:identifier>10.1371/journal.ppat.1014610.s018</dc:identifier>
          <dc:relation>https://figshare.com/articles/figure/_p_AlphaFold_prediction_and_cellular_validation_of_the_interaction_between_TET2_and_Vpr_p_/34047911</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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