Back

Scalable Production of a De Novo SARS-CoV-2 Antiviral miniprotein in Escherichia coli

Shin, J.; KIm, E.-m.; Jang, J.-h.; Jee, S.-w.; Kim, S.-h.; Yu, S.; Yoon, M.; Craig, D.; Swoyer, R.; Alamuri, P.; Price, A.; Patel, S.; Ravichandran, R.; Carter, L.; Pallerla, S.

2026-06-24 bioengineering
10.64898/2026.06.23.734092 bioRxiv
Show abstract

The rapid emergence of SARS-CoV-2 variants that evade neutralizing antibodies underscores the need for next-generation antiviral biologics that combine molecular precision with scalable, cost-effective manufacturing. Computationally designed miniproteins targeting the receptor-binding domain (RBD) of the spike protein offer a compelling alternative to monoclonal antibodies due to their small size, high thermal stability, and compatibility with microbial expression systems. Here we report the end-to-end development and cGMP production of IPD-52520, a de novo antiviral miniprotein, using an optimized E. coli platform. Two miniprotein candidates, a homotrimeric construct (Trimer is referred to as IPD-52520, 17 kDa) and a tandem fusion (Daisy is referred to as IPD-52521, 25 kDa), were evaluated in parallel through systematic optimization of strain selection, media composition, fed-batch fermentation, inclusion-body solubilization, refolding, and chromatographic purification. The Trimer was downselected as the lead molecule based on superior preclinical efficacy, favorable pharmacokinetic properties, and higher volumetric manufacturing yields. The optimized process delivers approximately 2 g/L of purified protein at greater than 90% purity. Scale-up from 5 L to 50 L under cGMP conditions demonstrated excellent batch-to-batch reproducibility across six independent batches, supporting nonclinical and Phase 1 clinical supply. Comprehensive biophysical characterization confirmed a well-folded, predominantly alpha-helical trimer (Tm = 73.4 {degrees}C; polydispersity = 1.005) with an intact primary structure and strong target-binding affinity (KD < 1 pM). Real-time stability studies indicate that the drug substance is stable at 2-8 {degrees}C for at least 12 months, with ongoing stability studies. These results demonstrate the feasibility of translating computationally designed antiviral miniproteins into manufacturable biologics and provide a platform applicable to rapid-response therapeutics against current and future pandemic threats.

Matching journals

The top 12 journals account for 50% of the predicted probability mass.

1
mAbs
32 papers in training set
Top 0.1%
7.8%
2
Microbial Cell Factories
27 papers in training set
Top 0.1%
6.7%
3
Biotechnology and Bioengineering
53 papers in training set
Top 0.1%
5.5%
4
ACS Synthetic Biology
287 papers in training set
Top 0.7%
4.8%
5
Trends in Biotechnology
12 papers in training set
Top 0.1%
3.5%
6
Protein Science
246 papers in training set
Top 1%
3.4%
7
New Biotechnology
12 papers in training set
Top 0.1%
3.2%
8
ACS Chemical Biology
167 papers in training set
Top 0.8%
3.2%
9
ACS Omega
105 papers in training set
Top 0.6%
3.2%
10
PLOS ONE
5266 papers in training set
Top 38%
3.2%
11
Frontiers in Bioengineering and Biotechnology
98 papers in training set
Top 0.5%
3.2%
12
Molecular Pharmaceutics
16 papers in training set
Top 0.1%
3.1%
50% of probability mass above
13
ACS Central Science
71 papers in training set
Top 0.5%
2.4%
14
International Journal of Biological Macromolecules
76 papers in training set
Top 0.8%
2.1%
15
Protein Engineering, Design and Selection
15 papers in training set
Top 0.1%
2.1%
16
Nature Communications
5641 papers in training set
Top 43%
2.0%
17
RSC Chemical Biology
39 papers in training set
Top 0.4%
1.5%
18
Cell Chemical Biology
94 papers in training set
Top 1.0%
1.4%
19
Biochemistry
148 papers in training set
Top 2%
1.4%
20
Computational and Structural Biotechnology Journal
242 papers in training set
Top 4%
1.3%
21
Journal of Biotechnology
11 papers in training set
Top 0.2%
1.1%
22
Metabolic Engineering
75 papers in training set
Top 0.6%
1.1%
23
Advanced Science
286 papers in training set
Top 7%
1.1%
24
Bioengineering & Translational Medicine
21 papers in training set
Top 0.4%
1.1%
25
Scientific Reports
3612 papers in training set
Top 65%
1.1%
26
Angewandte Chemie International Edition
93 papers in training set
Top 1%
1.1%
27
Protein Expression and Purification
13 papers in training set
Top 0.1%
1.1%
28
ACS Infectious Diseases
82 papers in training set
Top 1%
1.0%
29
Antibody Therapeutics
16 papers in training set
Top 0.2%
1.0%
30
Communications Biology
993 papers in training set
Top 30%
0.8%