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Directed evolution to enhance the catalytic activity of human arginase 1
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Cui-yue FENG1, Chen-yu WANG1, Meng-jia TANG1, Shuai FAN2, Zhao-yong YANG2, *, Zhi-fei ZHANG1, *
Acta Pharmaceutica Sinica | 2024, 59(12) : 3402 - 3408
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Acta Pharmaceutica Sinica | 2024, 59(12): 3402-3408
Directed evolution to enhance the catalytic activity of human arginase 1
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Cui-yue FENG1, Chen-yu WANG1, Meng-jia TANG1, Shuai FAN2, Zhao-yong YANG2, *, Zhi-fei ZHANG1, *
Affiliations
  • 1. School of Pharmacy, North China University of Science and Technology, Tangshan 063210, China
  • 2. Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, China
Published: 2024-12-12 doi: 10.16438/j.0513-4870.2024-0489
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Arginase 1 deficiency (ARG1-D) is a rare genetic metabolic disorder that leads to progressive spastic paralysis, cognitive impairment, and seizures. Recombinant human arginase 1 (rhArg1) is a potential therapeutic agent for this condition, but its clinical application is limited by low activity and short half-life. In this study, we employed directed evolution to address these issues. A random mutation library of rhArg1 was constructed using error-prone PCR, and high-throughput screening was used to identify mutants with enhanced activity. Site-saturation mutagenesis was also performed to investigate the effects of residues R21 and V182 on enzyme activity. Our findings revealed that under reaction conditions devoid of Mn2+, the kcat values of the mutants V182D, V182S, V182H, and R21N increased by 2.0, 1.9, 1.7, and 1.3 times respectively, compared to rhArg1. The kcat/Km values of mutants V182D, V182S, R21D, and R21N were 2.1, 1.7, 1.4, and 1.4 times higher than those of rhArg1, respectively. Additionally, mutants R21D and V182L showed enhanced substrate affinity. Through directed evolution and site-saturation mutagenesis, we successfully obtained rhArg1 mutants with improved activity, thereby enhancing its potential for clinical application.

arginase 1 deficiency  /  recombinant human arginase 1  /  directed evolution  /  site-saturation mutagenesis
Cui-yue FENG, Chen-yu WANG, Meng-jia TANG, Shuai FAN, Zhao-yong YANG, Zhi-fei ZHANG. Directed evolution to enhance the catalytic activity of human arginase 1[J]. Acta Pharmaceutica Sinica, 2024 , 59 (12) : 3402 -3408 . DOI: 10.16438/j.0513-4870.2024-0489
Year 2024 volume 59 Issue 12
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doi: 10.16438/j.0513-4870.2024-0489
  • Receive Date:2024-05-21
  • Online Date:2025-11-24
  • Published:2024-12-12
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  • Received:2024-05-21
  • Revised:2024-07-30
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    1. School of Pharmacy, North China University of Science and Technology, Tangshan 063210, China
    2. Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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