<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>44(5)</volume><submitter>Jia XM</submitter><pubmed_abstract>CKLF (chemokine-like factor)-MARVEL transmembrane domain containing protein 6 (CMTM6) is a novel regulator to maintain the stability of PD-L1. CMTM6 can colocalize and interact with PD-L1 on the recycling endosomes and cell membrane, preventing PD-L1 from lysosome-mediated degradation and proteasome-mediated degradation thus increasing the half-life of PD-L1 on the cell membrane. The difficulties in obtaining stable full-length PD-L1 and CMTM6 proteins hinder the research on their structures, function as well as related drug development. Using lauryl maltose neopentyl glycol (LMNG) as the optimized detergent and a cell membrane mimetic strategy, we assembled a stable membrane-bound full-length CMTM6-PD-L1 complex with amphipol A8-35. When the PD-1/PD-L1-CMTM6 interactions were analyzed, we</pubmed_abstract><journal>Acta pharmacologica Sinica</journal><pagination>1095-1104</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10104848</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Construction of stable membranal CMTM6-PD-L1 full-length complex to evaluate the PD-1/PD-L1-CMTM6 interaction and develop anti-tumor anti-CMTM6 nanobody.</pubmed_title><pmcid>PMC10104848</pmcid><pubmed_authors>Yu XL</pubmed_authors><pubmed_authors>Jia XM</pubmed_authors><pubmed_authors>Chen RQ</pubmed_authors><pubmed_authors>Geng Y</pubmed_authors><pubmed_authors>Long YR</pubmed_authors><pubmed_authors>Gong LK</pubmed_authors></additional><is_claimable>false</is_claimable><name>Construction of stable membranal CMTM6-PD-L1 full-length complex to evaluate the PD-1/PD-L1-CMTM6 interaction and develop anti-tumor anti-CMTM6 nanobody.</name><description>CKLF (chemokine-like factor)-MARVEL transmembrane domain containing protein 6 (CMTM6) is a novel regulator to maintain the stability of PD-L1. CMTM6 can colocalize and interact with PD-L1 on the recycling endosomes and cell membrane, preventing PD-L1 from lysosome-mediated degradation and proteasome-mediated degradation thus increasing the half-life of PD-L1 on the cell membrane. The difficulties in obtaining stable full-length PD-L1 and CMTM6 proteins hinder the research on their structures, function as well as related drug development. Using lauryl maltose neopentyl glycol (LMNG) as the optimized detergent and a cell membrane mimetic strategy, we assembled a stable membrane-bound full-length CMTM6-PD-L1 complex with amphipol A8-35. When the PD-1/PD-L1-CMTM6 interactions were analyzed, we</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 May</publication><modification>2026-06-01T23:37:12.701Z</modification><creation>2026-05-23T03:08:05.004Z</creation></dates><accession>S-EPMC10104848</accession><cross_references><pubmed>36418428</pubmed><doi>10.1038/s41401-022-01020-3</doi></cross_references></HashMap>