<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jeong HJ</submitter><funding>JSPS</funding><pagination>13285-97</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4168482</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(7)</volume><pubmed_abstract>Antibody-based sensors have made outstanding contributions to the fields of molecular biology and biotechnology. Our group recently developed a novel powerful fluorescent immunosensor strategy named Quenchbody (Q-body), which has been applied to the detection of a range of antigens in a rapid, simple, and sensitive manner. However, there were some Q-bodies whose fluorescence response was limited, especially for detecting protein antigens. With the aim of improving this issue, here we made twelve types of Q-bodies incorporated with different number and position of TAMRA fluorophore in the single chain Fv of HyHEL-10, an anti-hen egg lysozyme antibody, as a model. By measuring the fluorescence intensity and its antigen dependency, it was revealed that VL-VH type Q-bodies labeled at a non-CDR</pubmed_abstract><journal>Sensors (Basel, Switzerland)</journal><pubmed_title>Strategy for making a superior Quenchbody to proteins: effect of the fluorophore position.</pubmed_title><pmcid>PMC4168482</pmcid><funding_grant_id>Grant-in-Aid for Challenging Exploratory Research (25123456)</funding_grant_id><funding_grant_id>Grant-in-Aid for Scientific Research (B24360336)</funding_grant_id><pubmed_authors>Jeong HJ</pubmed_authors><pubmed_authors>Ueda H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Strategy for making a superior Quenchbody to proteins: effect of the fluorophore position.</name><description>Antibody-based sensors have made outstanding contributions to the fields of molecular biology and biotechnology. Our group recently developed a novel powerful fluorescent immunosensor strategy named Quenchbody (Q-body), which has been applied to the detection of a range of antigens in a rapid, simple, and sensitive manner. However, there were some Q-bodies whose fluorescence response was limited, especially for detecting protein antigens. With the aim of improving this issue, here we made twelve types of Q-bodies incorporated with different number and position of TAMRA fluorophore in the single chain Fv of HyHEL-10, an anti-hen egg lysozyme antibody, as a model. By measuring the fluorescence intensity and its antigen dependency, it was revealed that VL-VH type Q-bodies labeled at a non-CDR</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Jul</publication><modification>2025-04-03T22:43:03.042Z</modification><creation>2019-06-06T13:17:23Z</creation></dates><accession>S-EPMC4168482</accession><cross_references><pubmed>25057138</pubmed><doi>10.3390/s140713285</doi></cross_references></HashMap>