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ADC Development with Fully Human Platforms

Novel technologies for next-generation antibody drug conjugates
Overview
Conjugation
Characterization

Fully Human Discovery Platform for ADC Innovation

Our ADC capabilities are built on the strength of Harbour Mice® technology, delivering fully human antibodies optimized for therapeutic development. From classical H2L2 antibodies to compact HCAbs, our discovery platform generates highly developable constructs ideally suited for ADC applications. These antibodies serve as the foundation for Nona’s integrated ADC platform, which combines proprietary linker design, site-specific conjugation, and advanced characterization. Designed with scalability and manufacturability in mind, this end-to-end approach ensures efficiency and confidence from discovery to IND.

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Advanced Conjugation Technologies

Designed for flexibility, the platform offers both a validated linker–payload library to accelerate development and customized linker design for specific therapeutic requirements. Each design is optimized for stability and efficient release, considering tumor-associated proteases, payload mechanism of action, and internalization pathways. The platform supports lysine- or cysteine-based conjugation with small molecules, peptides, antisense oligonucleotides, and antibody-based constructs, with workflows scalable from microgram studies to gram-level production.

Customized Linker–Drug Design
HCAb DAR2 Site-Specific Conjugation Platform

DAR2 enables precise, site-specific drug attachment with a consistent drug-to-antibody ratio of two. This control enhances stability and therapeutic index while avoiding the liabilities of conventional high-DAR species, providing a reproducible and manufacturable path for ADC development.

  • It will shorten the workflow for positive plasma cell screening from months to a single day.

  • The high throughput screening with 14K or 20K chips dramatically decreases labor costs for screening more than 10,000 cells.

  • Direct screening with individual plasma cells prevents the diversity loss/bias during hybridoma screening.

Smaller size: ~85 kDa
  • Better tissue penetration
Access special epitope
  • Better specificity
  • Better internalization
Site-specific conjugation
  • High homogeneous product
  • High stability with conserved natural disulfide bonds
Fully human antibody sequences
  • No additional tags
  • No non-natural amino acids
  • No changes to glycosylation patterns
Simple conjugation
  • Good manufacturability
Flexibility
  • Expand to other modalities (e.g., BsAb)

Antibody Discovery in a “Single Day” by Beacon® Technology

Berkeley Lights Beacon® Optofluidic System

Beacon® can support the separation and screening of 10,000+ cells in a single run with one 14K or 20K OptoSelect chip. Enriched plasma cells are individually loaded into NanoPen chambers on the chip. Our proprietary medium preserves the viability and facilitates antibody secretion of these plasma cells. Multiple in-chip assays can be sequentially performed to screen those plasma cells, and the cells with desired signals wll beare selected and exported one by one through OEP technology. The entire workflow is completed in just one day.

High Throughput Chip

Each 20K OptoSelect chip has 20,000 individual NanoPen chambers and can separate and screen up to 20,000 cells within a single run.

Versatile In-Chip Assays

With real-time fluorescent microscopy technology, different assays could be performed in-chip for plasma cell screening, including:

  • Antigen beads binding assay
  • Cell binding assay
  • Competition assay
  • Reporter cell assay

All these advantages make SBC platform to become highly efficient and robust antibody discovery platform.

Precisely Single Cell Exporting

Opto-electro positioning (OEP) technology precisely manipulates and unloads cells to 96-well plates preloaded with single-cell sequencing reagents.

  • It will shorten the workflow for positive plasma cell screening from months to a single day.

  • The high throughput screening with 14K or 20K chips dramatically decreases labor costs for screening more than 10,000 cells.

  • Direct screening with individual plasma cells prevents the diversity loss/bias during hybridoma screening.

ADC Characterization

Our ADC solution provides full-spectrum physicochemical and biological characterization to ensure the highest standards of efficacy, safety, and preclinical readiness. This integrated approach combines analytical methods with in vitro and in vivo validation to deliver actionable insights across every stage of development.

We offer a wide range of specialized assays and validation tools, including:

  • Physicochemical Characterization:
    Analytical tools such as LC-MS, SEC-MALS, and cIEF offer detailed insights into charge heterogeneity, molecular weight, DAR, conjugation stability, aggregation, and free drug residue monitoring.
  • In vitro Validation:
    Bioactivity studies include antigen binding, internalization, soluble antigen interference, cytotoxicity, and bystander killing.
  • In vivo Validation:
    Pharmacological models encompass PK studies, stability assessments, and efficacy testing in CDX, PDX, and heterogeneous tumor environments.

Attribute Analytical Methods
DAR HIC
UV
mass spec
RP-HPLC
Purity SEC (HMW & LMW species)
HIC (DAR0 content)
RP-HPLC (DAR0 content)
Residual free drugs RP-HPLC
Endotoxin Chromogenic LAL assay
Recombinant Factor C assay

Let’s Conjugate the Right Solution

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Explore Related Resources

Novel Linker Scientific Poster
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