<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pechlivani N</submitter><funding>British Heart Foundation</funding><funding>Diabetes UK</funding><funding>Wellcome Trust</funding><pagination>89-100</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11742610</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(1)</volume><pubmed_abstract>&lt;h4>Abstract&lt;/h4>Hypofibrinolysis is a documented abnormality in conditions with high risk of vascular occlusion. A key inhibitor of fibrinolysis is α2-antiplasmin (α2AP), and we hypothesize that the Affimer technology, comprising small conformational proteins with 2 9-amino-acid variable regions, can be used to modulate α2AP activity and facilitate fibrinolysis. Using a phage display system, a library of Affimers was screened against α2AP. A total of 28 α2AP-specific Affimers were isolated, of which 1, termed Affimer A11, inhibited protein function and enhanced fibrinolysis. Affimer A11 displayed a monomeric form and consistently reduced the lysis time of clots made from plasma samples of individuals with type 2 diabetes mellitus (n = 15; from 150.8 ± 100.9 to 109.8 ± 104.8 minutes) and t</pubmed_abstract><journal>Blood advances</journal><pubmed_title>Use of Affimer technology for inhibition of α2-antiplasmin and enhancement of fibrinolysis.</pubmed_title><pmcid>PMC11742610</pmcid><funding_grant_id>FS/IBSRF/22/25130</funding_grant_id><funding_grant_id>14/0005006</funding_grant_id><pubmed_authors>Tomlinson DC</pubmed_authors><pubmed_authors>Almutairi M</pubmed_authors><pubmed_authors>Tiede C</pubmed_authors><pubmed_authors>Ponnambalam S</pubmed_authors><pubmed_authors>Alsayejh B</pubmed_authors><pubmed_authors>Kietsiriroje N</pubmed_authors><pubmed_authors>Duval C</pubmed_authors><pubmed_authors>Simmons K</pubmed_authors><pubmed_authors>Gaule T</pubmed_authors><pubmed_authors>Ajjan RA</pubmed_authors><pubmed_authors>Pechlivani N</pubmed_authors><pubmed_authors>Phoenix F</pubmed_authors><pubmed_authors>Ariens RAS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Use of Affimer technology for inhibition of α2-antiplasmin and enhancement of fibrinolysis.</name><description>&lt;h4>Abstract&lt;/h4>Hypofibrinolysis is a documented abnormality in conditions with high risk of vascular occlusion. A key inhibitor of fibrinolysis is α2-antiplasmin (α2AP), and we hypothesize that the Affimer technology, comprising small conformational proteins with 2 9-amino-acid variable regions, can be used to modulate α2AP activity and facilitate fibrinolysis. Using a phage display system, a library of Affimers was screened against α2AP. A total of 28 α2AP-specific Affimers were isolated, of which 1, termed Affimer A11, inhibited protein function and enhanced fibrinolysis. Affimer A11 displayed a monomeric form and consistently reduced the lysis time of clots made from plasma samples of individuals with type 2 diabetes mellitus (n = 15; from 150.8 ± 100.9 to 109.8 ± 104.8 minutes) and t</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jan</publication><modification>2026-06-02T20:11:34.592Z</modification><creation>2025-04-04T14:05:56.518Z</creation></dates><accession>S-EPMC11742610</accession><cross_references><pubmed>39504559</pubmed><doi>10.1182/bloodadvances.2024014235</doi></cross_references></HashMap>