Zmyslia Mariia, Capper Michael J, Grimmeisen Michael, Sartory Kerstin, Deuringer Benedikt, Abdelsalam Mohamed, Shen Kaiwei, Jung Manfred, Sippl Wolfgang, Koch Hans-Georg, Kaul Laurine, Süss Regine, Köhnke Jesko, Jessen-Trefzer Claudia
Institute of Organic Chemistry, University of Freiburg 79104 Freiburg im Breisgau Germany
School of Chemistry, University of Glasgow Glasgow G12 8QQ UK
RSC Chem Biol. 2024 Nov 4;6(1):21-35. doi: 10.1039/d4cb00127c.
Nitroreductases are important enzymes for a variety of applications, including cancer therapy and bioremediation. They often require encapsulation to improve stability and activity. We focus on genetically encoded encapsulation of nitroreductases within protein capsids, like encapsulins. Our study showcases the encapsulation of nitroreductase NfsB as functional dimers within encapsulins, which enhances protein activity and stability in diverse conditions. Mutations within the pore region are beneficial for activity of the encapsulated enzyme, potentially by increasing diffusion rates. Cryogenic electron microscopy reveals the overall architecture of the encapsulated dimeric NfsB within the nanoreactor environment and identifies multiple pore states in the shell. These findings highlight the potential of encapsulins as versatile tools for enhancing enzyme performance across various fields.
硝基还原酶是用于多种应用(包括癌症治疗和生物修复)的重要酶。它们通常需要进行封装以提高稳定性和活性。我们专注于在蛋白质衣壳(如封装菌素)内对硝基还原酶进行基因编码封装。我们的研究展示了将硝基还原酶NfsB作为功能二聚体封装在封装菌素内,这在不同条件下增强了蛋白质的活性和稳定性。孔区域内的突变有利于封装酶的活性,可能是通过提高扩散速率实现的。低温电子显微镜揭示了纳米反应器环境中封装的二聚体NfsB的整体结构,并确定了外壳中的多种孔状态。这些发现突出了封装菌素作为跨领域增强酶性能的通用工具的潜力。