生物催化
超分子化学
肽
酶
化学
组合化学
生物化学
纳米技术
材料科学
有机化学
催化作用
反应机理
分子
作者
Madeline Fuchs,Lucas Melgar,Bethsymarie Soto Morales,Dillon T. Seroski,Jennifer A Simonovich,Isabella Pinto,Chen Lu,Gianna Scibilio,Renjie Liu,Abigail M. Ziegler,Juanpablo Olguin,Arun Wanchoo,Ayumi Shigemoto,Dorina Avram,Benjamin G. Keselowsky,Gregory A. Hudalla
标识
DOI:10.1101/2024.09.06.611628
摘要
Enzyme therapeutics are often compromised by poor accumulation within target tissues, necessitating high doses that can exacerbate off-target effects. We report an injectable supramolecular enzyme-peptide gel platform for prolonged local enzyme retention in vivo . The gel is based on CATCH(+/-) ( C o- A ssembling T ags based on CH arge-complementarity), cationic and anionic peptide pairs that form β-sheet fibrils upon mixing 1 . Enzymes recombinantly fused to CATCH(-) peptide integrate into CATCH(+/-) β-sheet fibrils during assembly, resulting in an enzyme-peptide gel. Catalytically-active gels were fabricated with four disparate enzymes: CATCH(-)-NanoLuc luciferase, CATCH(-)-cutinase, CATCH(-)-uricase, and CATCH(-)-adenosine synthase A. CATCH(-)-cutinase gels demonstrated tunability of the platform, while CATCH(-)-NanoLuc gels demonstrated prolonged tissue retention relative to soluble enzyme. CATCH(-)-uricase gels resolved localized inflammation in a gout model, while CATCH(-)-adenosine synthase A gels suppressed localized lipopolysaccharide-induced inflammation. Modular and tunable enzyme content, coupled with prolonged tissue retention, establish CATCH enzyme-peptide gels as a generalizable vehicle for effective local therapeutic biocatalysis.
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