Supramolecular Enzyme-Peptide Gels for Localized Therapeutic Biocatalysis

Madeline Fuchs, Dillon T Seroski, Bethsymarie Soto Morales, Lucas Melgar, Giannia Scibilio, Abigail Ziegler, Renjie Liu, Benjamin G Keselowsky, Gregory A Hudalla
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Abstract

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(+/-) (Co-Assembling Tags based on CHarge-complementarity), cationic and anionic peptide pairs that form β-sheet fibrils upon mixing. 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.
用于局部治疗生物催化的超分子酶肽凝胶
酶疗法往往因在靶组织内蓄积不良而受到影响,必须使用大剂量,否则会加剧脱靶效应。我们报告了一种可注射的超分子酶肽凝胶平台,用于延长体内局部酶的保留时间。这种凝胶基于 CATCH(+/-)(Co-Assembling Tags based on CHarge-complementarity),阳离子和阴离子肽对在混合后形成 β 片状纤维。与 CATCH(-) 肽重组融合的酶在组装过程中整合到 CATCH(+/-) β 片纤维中,形成酶肽凝胶。用四种不同的酶制造了具有催化活性的凝胶:CATCH(-)-cutinase 凝胶展示了平台的可调性,而 CATCH(-)-NanoLuc 凝胶则展示了与可溶性酶相比更长的组织保留时间。CATCH(-)-尿酸酶凝胶解决了痛风模型中的局部炎症,而CATCH(-)-腺苷合成酶A凝胶抑制了脂多糖诱导的局部炎症。模块化和可调整的酶含量,加上长时间的组织保留,使 CATCH 酶肽凝胶成为一种可用于有效局部治疗生物催化的通用载体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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