Newsletter | January 29, 2024

01.29.24 -- Why Lactococcus Lactis Might Be The Best Membrane Protein Factory

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The Importance Of Bioproduction Analytics In Cell Culture Media Optimization

To establish an economically feasible biopharmaceutical manufacturing process, it's vital for developers to meet their targets during process development. Accurate and meaningful analytics can help in streamlining the cell culture media development process, optimizing a formulation, troubleshooting issues, and achieving long-term success. Learn more about the importance of analytical techniques, including how a multiomics analysis can help create models to further advance formulation development.

FEATURED EDITORIAL

Why Lactococcus Lactis Might Be The Best Membrane Protein Factory

The bacteria lactococcus lactis has emerged as a promising alternative expression system for membrane proteins, which are difficult to manufacture. L. lactis is inexpensive and easy to grow. Importantly, it doesn't produce endotoxins, making it a good fit for therapeutic applications.

Biotech Is Back With Allan Shaw

The Business of Biotech podcast took a trip to San Francisco for the JP Morgan Healthcare Conference. The results of that trip will feed the next several weeks of Business of Biotech podcast programming, and we're kicking things off with everyone's favorite life sciences CFO, Allan Shaw. 

INDUSTRY INSIGHTS

Strategies, Emerging Technologies For mAb Capture

Explore opportunities with the introduction of high-capacity protein A resins, how and when multicolumn chromatography is beneficial, and how emerging technologies can address bottlenecks.

Challenges And Solutions For Viral Product Development, Manufacturing

To execute complex viral product manufacturing, a service provider needs expertise in adherent cell culture capabilities, cell line productivity, and the intricacies associated with these products.

What Parameters Can Help You Create Biologics Developability Profiles?

Developability profiles of biologics candidates help you avoid risk by collecting many quality attributes. Learn which attributes are evaluated during development and approaches for their measurement.

Building A Fully Single-Use Process: Protein A Membrane Devices

Learn how a fully disposable upstream and downstream platform process in antibody production can increase production timelines, enhance scalability, and reduce risk in biologics manufacturing.

AAV Thermostability Assessment With Microflow Imaging

This study demonstrates a microflow imaging system's ability to evaluate AAV9 particle purity and stability when subjected to heat stress at two different temperatures: 37 °C and 75 °C.

Plan Your CDMO Search On A Foundation For Long-Term Success

Capacity constraints typically are accompanied by other challenges, including missed timelines, defect rates, and overall decreased satisfaction with pharma companies’ bioprocessing CDMOs.

Characterize T-Cell Exhaustion And Hypofunctionality In Cancer

Investigate what drives the hypofunctional state of T cells in ICB-nonresponsive cancers through the characterization of CD8+ T-cell functionality in different tumor types. 

Why Is E&L Testing Important For Single-Use Connectors?

A critical issue when transitioning from stainless steel to plastic equipment is the presence of extractables and leachables (E&L). BPOG testing on single-use connectors mitigates the risks.

Elastomer Plungers With Barrier Film For COVID-19 Vaccines

Minimize the risks of accelerated drug development processes and the potential use of new vaccine platform technologies with the use of a unique, laminated elastomer plunger.

Streamline Process Characterization For Successful Validation Campaigns

Explore how a stepwise approach for process characterization can help target the right experimental design and be tailored for different programs based on prior knowledge and experience.

Drug Product Process Characterization For Liquid And Lyophilized DP

Explore important initial steps to consider and implement during the process design phase, which is a prerequisite to a successful PPQ campaign and readiness for commercial manufacturing.

SOLUTIONS

Biopharmaceutical Cleaning Validation

Fill/Finish Solution: Maximize Drug Product Recovery

Benchtop For Lipid Nanoparticle R&D And Preclinical Development

Echo 650 Series Acoustic Liquid Handlers For Assay Miniaturization

Flexible And Agile Biomanufacturing Solutions

Monitor And Control Both Glucose And Lactate In Real Time

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