Two-in-one protein tag enables the soluble expression and calcium-dependent purification of single-chain antibody fragments

Single-chain variable fragments (scFvs) antibodies are used in diagnostic and therapeutic biopharmaceuticals. However, its production is limited due to insoluble expression and lack of a universal purification ligand. Here, we report a novel two-in-one protein tag, termed CSQ-tag, utilizing a calsequestrin (CSQ) protein to enable the soluble expression and calcium-dependent purification for scFvs. The CSQ-tag enhanced the solubility of four different therapeutic scFvs with an average solubility of 83.8 ± 4.6% in the BL21(DE3) strain, despite its reducing cytoplasmic environment. Compared to other tags, CSQ-tag showed superior solubility, with 1.8-fold higher solubility than MBP-tag across four scFvs. The solubility enhancement of the CSQ-tag is attributed to two main characteristics: highly acidic sequences with a low isoelectric point of 3.95, and intrinsically disordered protein properties. Furthermore, CSQ-tag can cost-effectively purify therapeutic scFvs with high purity over 95% using the calcium-dependent phase transition properties. Importantly, the anti-VEGF-scFv produced with the CSQ-tag showed a binding affinity of 25.8 pM, similar to that of the existing therapeutic brolucizumab. Therefore, CSQ-tag can significantly improve productivity and simultaneously maintain scFvs' functional integrity, thereby serving as a promising tool for universal expression and purification of therapeutic scFvs.

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Journal
Communications Biology
Published
2026-01-26
DOI
https://doi.org/10.1038/s42003-026-09611-0
Primary Topic
Monoclonal and Polyclonal Antibodies Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Two-in-one protein tag enables the soluble expression and calcium-dependent purification of single-chain antibody fragments

Heesun Park, Sangyong Jon, Kyuhyuk Im, Seho Park et al.
Communications Biology
Monoclonal and Polyclonal Antibodies Research
article

Two-in-one protein tag enables the soluble expression and calcium-dependent purification of single-chain antibody fragments

Heesun Park, Sangyong Jon, Kyuhyuk Im, Seho Park, Suhyeon Jeong, Sunghyun Kim, Sanguine Byun, Jonghwan Lee
article en

Abstract

Single-chain variable fragments (scFvs) antibodies are used in diagnostic and therapeutic biopharmaceuticals. However, its production is limited due to insoluble expression and lack of a universal purification ligand. Here, we report a novel two-in-one protein tag, termed CSQ-tag, utilizing a calsequestrin (CSQ) protein to enable the soluble expression and calcium-dependent purification for scFvs. The CSQ-tag enhanced the solubility of four different therapeutic scFvs with an average solubility of 83.8 ± 4.6% in the BL21(DE3) strain, despite its reducing cytoplasmic environment. Compared to other tags, CSQ-tag showed superior solubility, with 1.8-fold higher solubility than MBP-tag across four scFvs. The solubility enhancement of the CSQ-tag is attributed to two main characteristics: highly acidic sequences with a low isoelectric point of 3.95, and intrinsically disordered protein properties. Furthermore, CSQ-tag can cost-effectively purify therapeutic scFvs with high purity over 95% using the calcium-dependent phase transition properties. Importantly, the anti-VEGF-scFv produced with the CSQ-tag showed a binding affinity of 25.8 pM, similar to that of the existing therapeutic brolucizumab. Therefore, CSQ-tag can significantly improve productivity and simultaneously maintain scFvs' functional integrity, thereby serving as a promising tool for universal expression and purification of therapeutic scFvs.

Communications BiologyVol. 9(1)
Korea Advanced Institute of Science and Technology (KR), Yonsei University (KR), Korea Institute of Ceramic Engineering and Technology (KR), ToolGen (South Korea) (KR)
National Research Foundation, Ministry of SMEs and Startups, Ministry of Science and ICT, South Korea, Korea Institute of Ceramic Engineering and Technology
Openalex Percentile: Top 79%
Monoclonal and Polyclonal Antibodies Research
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