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Expression, purification, and functional identification of immunoglobulin degrading enzyme IdeS in Escherichia coli
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Si-han ZHOU, Min-zhi LIU, Yan YANG, Wei WANG*
Acta Pharmaceutica Sinica | 2022, 57(7) : 2234 - 2239
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Acta Pharmaceutica Sinica | 2022, 57(7): 2234-2239
Original Articles
Expression, purification, and functional identification of immunoglobulin degrading enzyme IdeS in Escherichia coli
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Si-han ZHOU, Min-zhi LIU, Yan YANG, Wei WANG*
Affiliations
  • State Key Laboratory of Bioactive Substance and Function of Natural Medicines, NHC Key Laboratory of Natural Drug Biosynthesis, Institute of Materia Medica, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100050, China
Published: 2022-07-12 doi: 10.16438/j.0513-4870.2022-0364
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In the process of evolution, pathogenic Streptococcus pyogenes secretes an immunoglobulin G-degrading enzyme IdeS which can specifically cleave the hinge region of immunoglobulin G in order to escape the immune response against the host. On the one hand, IdeS can be used for IgG fingerprinting as a tool enzyme combined with mass spectrometry technology. On the other hand, IdeS can be used to treat the antibody-responsive diseases produced by autoimmunity as a therapeutic protein. In this study, the backbone of plasmid pCold was used to construct two expression vectors of recombinant protein IdeS, which were heterologously expressed in Escherichia coli Shuffle T7. After purification by affinity chromatography, the recombinant IdeS activity was detected and their activity differences between the two were compared. Among them, the yield of the recombinant IdeS containing the His6-tag at the N-terminus was 4 mg·L-1, and the cleavage reaction with antibody IgG1 at 1∶200 (m/m) at 37 ℃ for 30 min could complete. However, the yield of the recombinant IdeS containing both the N-terminal His6 tag and the C-terminal silica affinity tag (silica bing peptide, SiBP) is 1.5 mg·L-1, and the degradation reaction with antibody IgG1 at 1∶20 (m/m) at 37 ℃ for 30 min could reach the end. The C-terminal fusion peptide has a great influence on the yield and activity of IdeS, which is not conducive to subsequent application in drug development. Above all, the recombinant IdeS containing the His6-tag at the N-terminus expressed by this system has high activity and can fully meet the needs of antibody drug development and mapping analysis of IgG.

immunoglobulin G-degrading enzyme  /  heterologous expression  /  IgG fingerprinting  /  donor-specific antibody
Si-han ZHOU, Min-zhi LIU, Yan YANG, Wei WANG. Expression, purification, and functional identification of immunoglobulin degrading enzyme IdeS in Escherichia coli[J]. Acta Pharmaceutica Sinica, 2022 , 57 (7) : 2234 -2239 . DOI: 10.16438/j.0513-4870.2022-0364
Year 2022 volume 57 Issue 7
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Article Info
doi: 10.16438/j.0513-4870.2022-0364
  • Receive Date:2022-03-28
  • Online Date:2025-12-23
  • Published:2022-07-12
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  • Received:2022-03-28
  • Revised:2022-05-31
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    State Key Laboratory of Bioactive Substance and Function of Natural Medicines, NHC Key Laboratory of Natural Drug Biosynthesis, Institute of Materia Medica, Peking Union Medical College and Chinese Academy of Medical Sciences, 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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