MiMode™ PuraBead® HL4
Product overview
HCPure™ is a mixed-mode resin designed with the removal of host cell proteins (HCP) in mind. This unique resin is composed of a proprietary mixed-mode ligand attached to PuraBead® 6HF agarose bead support. HCPure™ has a unique operational space compared to other commercially available products and can provide alternative strategies for the removal of problemative HCPs. Whilst selectively binding host cell proteins, HCPure™ can also remove host cell DNA, endotoxin, light chain IgG, and high molecular weight aggregates, to yield highly purified biological products with minimal target protein losses.
Due to its highly selective nature and ability to be tuned, by varying the chromatography conditions, HCPure™ removes impurities from a number of different expression systems, including, but not limited to CHO, E. coli, HEK 293, Pichia Pastoris, Saccharomyces Cerevisiae, and Spodoptera frugiperda (Sf9 and Sf21).
What are the key features of HCPure™?- Removes host cell proteins, host cell DNA, endotoxin, light chain IgG, and high molecular weight aggregates
- Works with broad range of feedstocks generated from multiple expression systems
- Fostering a unique operational space compared to other commercially available products, providing alternative HCP removal strategies
- Demonstrated consistent performance across a broad pH and conductivity ranges
- Suitable for applications such as antibody and antibody derivative workflows, recombinant proteins, lentivirus, and AAV
Host cell proteins: Challenges in mAb polishing
Optimizing the mAb polishing step is essential because no single solution fits all, and the process requires balancing trade-offs between yield, purity, time, and scalability. Variations in impurities from different expression systems, as well as differences in antibody size, charge, isoelectric point (pI), and stability necessitate tailored polishing strategies.
While the traditional method of mAb purification using Protein A capture, cation-exchange (CEX) bind-and-elute, and anion-exchange (AEX) flow-through steps is a good starting point for purification, it is not suitable for all mAb products. Challenges that must be addressed include protein instability in high-salt CEX elution and the presence of problematic HCPs that ion exchange alone fails to fully separate from the mAb product.
Unique operational space: Chemical space mapping
HCPure™ stands out for its unique ligand composition and distinct mode of action, as visualized in Figure 1, demonstrating the resins chemical space. Positioned to the right of the graph, it highlights its ability to leverage at least six different interaction mechanisms under varying conditions, offering superior versatility in protein purification. The graph highlights the differences of HCPure™ to other commercially available mixed-mode adsorbents, where the map demonstrates the comparable chemical properties, where similar binding resins cluster together. HCPure™ resin’s unique positioning emphasizes its distinct performance offering an alternative purification strategy for problematic HCPs.
Figure 1. Chemical space diagram of commercial mixed-mode adsorbents.
In application: Antibody polishing
The removal of HCPs is a universal challenge across all antibody and antibody derivatives. HCPure™ is a mixed mode resin with a different operational space compared to other commercially available products and can provide alternative strategies for problematic HCPs.
HCPure™, a mixed-mode resin was evaluated for the impact of pH and conductivity on IgG purification versus another commercially available adsorbent. Heat maps, a predictive modeling tool used to visualise results, identify the most effective purification conditions, which, for HCPure™ showed consistent performance across a broad pH range. The importance of screening various resins is highlighted in Figure 2, where the heat map which display HCP clearance and IgG yield, where red regions indicate optimal performance.
The HCPure™ resin demonstrated consistent performance across a broad pH and conductivity range, maintaining high HCP clearance and IgG yield with minimal variation. In contrast, the competitor resin showed a strong pH dependency with optimal performance at pH 6, but with significant drops in yield at higher pH values, indicated by blue regions. This suggests that the ligand chemistry of the competitor adsorbent, interacted differently with the IgG compared to the HCPure™ resin. As a result, increasing pH caused the antibody to bind to a greater degree in the competitor product, reducing the recovery in the non-bound and therefore diminishing yield.
Overall, the HCPure™ resin provides an alternative strategy for problematic HCPs in antibody and antibody derivative manufacture. With stable performance, this resin provides a flexible option for HCP purification compared to alternative products.
Figure 2. Heat map which displays optimal pH and conductivity for optimal HCP clearance (top row) and IgG yield (bottom row). Red regions indicate optimal performance and blue regions demonstrating poor performance. The heat map was used to determine optimal pH and conductivity for HCP log reduction and yield for an IgG produced in an HEK cell line.
To view the range of applications and technical notes available for HCPure™, visit the download section at the top of this page.
Astrea Bioseparations: A complete toolbox for antibody purification
As the demand for novel antibody formats grows, efficient screening of purification conditions becomes essential. Astrea Bioseparations has a broad range of purification resins, ranging from capture to polish, for mAb and other antibody formats. Using Astrea Bioseparations' toolbox approach, products, such as Fabsorbent™ F1P HF, HCPure™, Q PuraBead® and SP PuraBead® Edge, provide the market with additional choices for downstream processing workflows. Resins are provided in high-throughput screening formats to streamline discovery and purification. Combining smarter purification strategies and high-throughput screening options will help shape the future of biopharmaceutical development and commercialization of new drugs.
Simplified workflow integration and scalability
HCPure™ is designed for seamless integration into existing purification processes. Available in multiple column sizes for research or process-ready applications and bulk adsorbent slurry, ensuring scalability from lab-scale R&D to large-scale manufacturing.
HCPure™ is a solution trusted by industry players to ensuring safe, pure, and high-quality antibody products. It provides a powerful alternative over traditional monoclonal antibody capture & purification methods, helping manufacturers achieve efficiency, reliability, and compliance.
Product specifications
Feature | Description |
---|---|
Ligand | Proprietary synthetic chemical ligand |
Bead size (µm) | 90 ± 10 µm |
Matrix | PuraBead® PHF (Highly cross-linked 6% near-monodisperse agarose) |
Recommended operational flow rates | Up to 600 cm/h |
Operating pH | pH 4.0 to pH 8.0 (intermittent) |
pH stability | Long term (3 months) pH 3 to pH 12 |
Chemical stability | All commonly used aqueous buffers and co-solvents |
Cleaning/sanitization | 0.5 to 1.0 M NaOH |
Storage | 2–30°C, 20% ethanol |
Frequently asked questions
Product Information
MiMode™ PuraBead® HL4 is a mixed-mode chromatography resin designed to provide a versatile and cost-effective solution for biomolecule purification. Built on the robust PuraBead® 6HF base matrix, it combines aromatic hydrophobic and hydrogen-bonding interactions, enabling both bind-and-elute and flow-through polishing applications.
Unlike single-mode affinity solutions, MiMode™ PuraBead® HL4 offers broad selectivity, making it suitable as a platform technology across multiple molecule classes. The synthetic ligand ensures strong base stability, while the PuraBead® 6HF matrix delivers excellent flow properties and scalability from discovery through to large-scale manufacturing.
With a wide operational pH range, compatibility with common buffer systems, and straightforward cleaning using sodium hydroxide, MiMode™ PuraBead® HL4 integrates seamlessly into existing workflows. It is available in high-throughput screening formats as well as process-scale volumes, supporting both rapid development studies and commercial production needs.
Key features of MiMode™ PuraBead® HL4
- Mixed-mode ligand combining hydrophobic and hydrogen bond interactions.
- Broad selectivity for capture and polishing across diverse biomolecule types.
- Operates under mild conditions, supporting product quality and stability.
- Robust base stability and tolerance to cleaning with 1.0 M NaOH.
- High-flow, low-pressure PuraBead® 6HF matrix ensures easy scalability.
Example Applications
MiMode™ PuraBead® HL4 has been successfully applied in a variety of contexts, including:
- Antibody purification – Capture and polishing of antibodies, as well as fragments and engineered formats.
- Protein polishing – Removal of aggregates, host cell proteins, and other process-related impurities in flow-through mode.
- General protein purification – Versatile capture and separation of recombinant proteins with diverse physicochemical properties.
Simplified workflow integration and scalability
MiMode™ PuraBead® HL4 can be used in screening, process development, and large-scale manufacturing. Available in 96-well plates, pre-packed columns, and bulk slurry, it is designed to support flexible adoption into diverse purification strategies. Combined with Astrea Bioseparations’ wider toolbox of resins and services, MiMode™ PuraBead® HL4 provides an adaptable option for streamlining downstream processing.
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