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Antibody-siRNA Conjugate Development

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Antibody-siRNA conjugate delivery systems can be created by directly conjugating siRNA to various chemical groups within an antibody. Traditional antibody-siRNA conjugates mainly use natural lysine or reduced cysteine residues. CD Formulation offers cost-effective conjugation services and supports large-scale development for global clients.

What are Antibody-siRNA Conjugates?

Antibody-small interfering RNA (siRNA) conjugates (ARCs) combine the specificity of antibodies with siRNA's gene-targeting capabilities. This method uses antibodies for precise targeting and siRNAs for gene silencing, delivering therapeutic payloads to specific cells to inhibit gene expression. ARCs address challenges of inadequate siRNA targeting and limited circulation, offering a promising solution for targeted gene silencing and enhanced therapeutic efficacy.

Fig.1 Synthesis of antibody-siRNA conjugates (ARCs).Fig.1 Synthesis of antibody-siRNA conjugates. (CD Formulation)

Antibody-siRNA Conjugate Development Services

Customized Development of Antibody-siRNA Conjugates

The antibody-siRNA binding site is selected at the 3' end of the S gene, a region typically designed for specific recognition and binding. In antibody-siRNA synthesis services, the biotin-streptavidin system is commonly employed in the coupling reaction. This chemical coupling reaction leverages the high affinity between biotin and streptavidin to achieve efficient linkage of the antibody to the siRNA, ensuring the stability and functional integrity of the bicomponent throughout the synthesis process.

Antibody-siRNA Conjugate Optimization Services

Items Descriptions
Chemical Modification Modifying the terminal ends or sugar-phosphate backbone of siRNAs can enhance stability and reduce immunogenicity. Notable modifications, like 2'-O-methyl and phosphorothioate, improve siRNA nuclease resistance.
Length Optimization The length of siRNA is crucial for hybridization stability. An optimal length prevents the formation of unstable secondary structures while ensuring sufficient length to maintain hybridization stability.
Coupling Strategy Optimization Utilizing nucleic acid-antibody coupling methods, such as double-stranded hybridization, can enhance binding efficiency. It is essential to employ rapid and highly specific coupling techniques, as these double-stranded hybridization methods exhibit superior kinetic properties.
Structural Design Optimize the sequence and structure of the siRNA to prevent interference with the antibody binding site and to ensure the proper spatial conformation that facilitates binding.

General Workflow for Antibody-siRNA Conjugate Development Services

Fig.2 Workflow for antibody-siRNA conjugate development.Fig.2 Flow chart of antibody-siRNA conjugate development. (CD Formulation)

  • siRNA Design and Synthesis

Design specific siRNA based on the target sequence, ensuring high-purity synthesis that includes biotinylation modification at the 3' end for subsequent binding.

  • Antibody Selection and Biotinylation

We assist customers in selecting suitable antibodies and biotinylating them to ensure efficient binding to streptavidin.

  • Antibody-siRNA Complex Construction

Combine biotin-labeled siRNA with antibodies to form stable complexes and optimize binding conditions for better efficiency.

  • Quality Control

Remove unbound components using efficient purification techniques, such as gel filtration and ultrafiltration. Conduct quality control using various methods, including SDS-PAGE and mass spectrometry.

Advantages of Our Antibody-siRNA Conjugate Development Services

  • Combining siRNA with specific antibodies enables targeted delivery to specific cells or tissues.
  • Antibody binding protects siRNA from degradation, enhances stability, and increases its half-life and bioavailability in vivo.
  • Antibody-siRNA complexes minimize the immune response compared to traditional viral vectors, reducing the risk of adverse reactions.

Synthesis Platforms

Solid-Phase Synthesis Platforms - Solid-phase synthesis technology for developing antibody-siRNA complexes is an efficient and controlled method for preparing high-purity siRNAs, which can subsequently undergo biotinylation modifications.

Published Data

Technology: Antibody-siRNA is prepared by chemical synthesis technology

Journal: Signal transduction and targeted therapy

IF: 38.104

Published: 2022

Results:

This review examines various antibody types, their applications in cancer therapy, and recent clinical research advances. The authors discuss the mechanisms of action for different forms, including antibody-drug conjugates and bispecific antibodies. Advances in biotechnology have enabled the development of novel antibodies, leading to successful treatments for various cancers, especially in precise tumor immunotherapy.

Fig.3 Schematic of antibody-siRNA conjugatesFig.3 Schematic representation of antibody-siRNA conjugates (ARCs). (Jin S, et al., 2022

CD Formulation offers professional antibody-siRNA development services, including siRNA design and synthesis, antibody selection and modification, complex construction, purification, and validation. Our comprehensive approach ensures high-quality products and exceptional experimental results. For more information, please do not hesitate to contact us.

References

  1. Jin S, Sun Y, Liang X, et al. Emerging new therapeutic antibody derivatives for cancer treatment. Signal Transduct Target Ther. 2022, 7(1): 39.
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