<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Shin WR</submitter><funding>Korea Institute of Planning and Evaluation for Technology in Food, Agriculture, Forestry and Fisheries</funding><funding>National Research Foundation of Korea</funding><pagination>204</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9044640</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Glypican-3 (GPC3), a membrane-bound heparan sulfate proteoglycan, is a biomarker of hepatocellular carcinoma (HCC) progression. Aptamers specifically binding to target biomolecules have recently emerged as clinical disease diagnosis targets. Here, we describe 3D structure-based aptaprobe platforms for detecting GPC3, such as aptablotting, aptaprobe-based sandwich assay (ALISA), and aptaprobe-based imaging analysis.&lt;h4>Results&lt;/h4>For preparing the aptaprobe-GPC3 platforms, we obtained 12 high affinity aptamer candidates (GPC3_1 to GPC3_12) that specifically bind to target GPC3 molecules. Structure-based molecular interactions identified distinct aptatopic residues responsible for binding to the paratopic nucleotide sequences (nt-paratope) of GPC3 aptaprobes. Sandwichable and overlapped aptaprobes were selected through structural analysis. The aptaprobe specificity for using in HCC diagnostics were verified through Aptablotting and ALISA. Moreover, aptaprobe-based imaging showed that the binding property of GPC3_3 and their GPC3 specificity were maintained in HCC xenograft models, which may indicate a new HCC imaging diagnosis.&lt;h4>Conclusion&lt;/h4>Aptaprobe has the potential to be used as an affinity reagent to detect the target in vivo and in vitro diagnosing system.</pubmed_abstract><journal>Journal of nanobiotechnology</journal><pubmed_title>Structure based innovative approach to analyze aptaprobe-GPC3 complexes in hepatocellular carcinoma.</pubmed_title><pmcid>PMC9044640</pmcid><funding_grant_id>2020R1A6A1A06046235</funding_grant_id><funding_grant_id>NRF-2020R1A2C1009463</funding_grant_id><funding_grant_id>MAFRA_321108-04</funding_grant_id><pubmed_authors>Kim SY</pubmed_authors><pubmed_authors>Thai NQ</pubmed_authors><pubmed_authors>Oh IH</pubmed_authors><pubmed_authors>Min J</pubmed_authors><pubmed_authors>Choi W</pubmed_authors><pubmed_authors>Kim SC</pubmed_authors><pubmed_authors>Kim YH</pubmed_authors><pubmed_authors>Shin WR</pubmed_authors><pubmed_authors>Lee JP</pubmed_authors><pubmed_authors>Kim JH</pubmed_authors><pubmed_authors>Sekhon SS</pubmed_authors><pubmed_authors>Park DY</pubmed_authors><pubmed_authors>Cho BK</pubmed_authors><pubmed_authors>Ahn JY</pubmed_authors></additional><is_claimable>false</is_claimable><name>Structure based innovative approach to analyze aptaprobe-GPC3 complexes in hepatocellular carcinoma.</name><description>&lt;h4>Background&lt;/h4>Glypican-3 (GPC3), a membrane-bound heparan sulfate proteoglycan, is a biomarker of hepatocellular carcinoma (HCC) progression. Aptamers specifically binding to target biomolecules have recently emerged as clinical disease diagnosis targets. Here, we describe 3D structure-based aptaprobe platforms for detecting GPC3, such as aptablotting, aptaprobe-based sandwich assay (ALISA), and aptaprobe-based imaging analysis.&lt;h4>Results&lt;/h4>For preparing the aptaprobe-GPC3 platforms, we obtained 12 high affinity aptamer candidates (GPC3_1 to GPC3_12) that specifically bind to target GPC3 molecules. Structure-based molecular interactions identified distinct aptatopic residues responsible for binding to the paratopic nucleotide sequences (nt-paratope) of GPC3 aptaprobes. Sandwichable and overlapped aptaprobes were selected through structural analysis. The aptaprobe specificity for using in HCC diagnostics were verified through Aptablotting and ALISA. Moreover, aptaprobe-based imaging showed that the binding property of GPC3_3 and their GPC3 specificity were maintained in HCC xenograft models, which may indicate a new HCC imaging diagnosis.&lt;h4>Conclusion&lt;/h4>Aptaprobe has the potential to be used as an affinity reagent to detect the target in vivo and in vitro diagnosing system.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2022-07-23T19:10:32.499Z</modification><creation>2022-07-23T19:10:32.499Z</creation></dates><accession>S-EPMC9044640</accession><cross_references><pubmed>35477501</pubmed><doi>10.1186/s12951-022-01391-z</doi></cross_references></HashMap>