<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chintala S</submitter><funding>NIDDK NIH HHS</funding><funding>National Institute of Diabetes and Digestive and Kidney Diseases</funding><funding>School of Pharmacy, University of Missouri-Kansas City</funding><funding>University of Missouri</funding><pagination>1506-1514</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8906801</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7(4)</volume><pubmed_abstract>In this work, we have brought the release of glucagon under the control of light. The aim of this approach is to allow minimally invasive, two-hormone control of blood glucose. Glucagon has two major challenges associated with its therapeutic application: (1) the required amount and timing of glucagon release is highly variable, and (2) glucagon rapidly fibrillates in solution, forming aggregates that are inactive. We have developed a light activated glucagon trimer, in which we have joined three glucagon molecules via light cleaved linkers. We demonstrated that this material can be stimulated by light to release glucagon in a predictable manner. In addition, we demonstrated that in the absence of light, the trimer does not form fibrils and thus releases normal unfibrillated glucagon upon </pubmed_abstract><journal>ACS biomaterials science &amp; engineering</journal><pubmed_title>A Light Activated Glucagon Trimer with Resistance to Fibrillation.</pubmed_title><pmcid>PMC8906801</pmcid><funding_grant_id>DP3 DK106921</funding_grant_id><funding_grant_id>R01DK123689</funding_grant_id><funding_grant_id>R01 DK123689</funding_grant_id><funding_grant_id>DP3DK106921</funding_grant_id><pubmed_authors>Chintala S</pubmed_authors><pubmed_authors>Friedman SH</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Light Activated Glucagon Trimer with Resistance to Fibrillation.</name><description>In this work, we have brought the release of glucagon under the control of light. The aim of this approach is to allow minimally invasive, two-hormone control of blood glucose. Glucagon has two major challenges associated with its therapeutic application: (1) the required amount and timing of glucagon release is highly variable, and (2) glucagon rapidly fibrillates in solution, forming aggregates that are inactive. We have developed a light activated glucagon trimer, in which we have joined three glucagon molecules via light cleaved linkers. We demonstrated that this material can be stimulated by light to release glucagon in a predictable manner. In addition, we demonstrated that in the absence of light, the trimer does not form fibrils and thus releases normal unfibrillated glucagon upon </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Apr</publication><modification>2025-04-19T09:22:52.052Z</modification><creation>2025-04-19T09:22:52.052Z</creation></dates><accession>S-EPMC8906801</accession><cross_references><pubmed>33703874</pubmed><doi>10.1021/acsbiomaterials.1c00031</doi></cross_references></HashMap>