PepTalk 2017
PepTalk 2017
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Cambridge Healthtech Institute’s Ninth Annual
Protein Purification and Recovery
Streamlining Processes with Innovative Technologies
January 10-11, 2017 | Hilton San Diego Bayfront | San Diego, CA


Protein purification is the most costly and time-consuming process in the manufacture of proteins. Challenges are multiplied when purifying complex molecules, such as membrane proteins, bispecifics or antibody-drug conjugates. This leading purification meeting on Protein Purification and Recovery will explore how experts are optimizing processes to achieve pure protein while curtailing cost and time. Along with innovating “traditional” technologies such as Protein A and chromatography, leaders will also address alternatives and breakthroughs, such as continuous processing.

TUESDAY, JANUARY 10

1:00 pm Conference Registration

1:30 Refreshment Break in the Exhibit Hall with Poster Viewing

PURIFICATION STRATEGIES FOR CONQUERING DISEASE

2:00 Chairperson’s Opening Remarks

William Gillette, Ph.D., Principal Scientist, RAS Protein Production, and Deputy Director, Protein Expression Laboratory, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research (FNL)


Keynote Presentation

2:05 Advances in Purification Technologies Accelerate Vaccine Development

Yan-ping YangYan-ping Yang, Ph.D., Senior Director and Head, Bioprocess R&D North America, Sanofi Pasteur

Over the last 25 years, significant breakthroughs in bioprocesses have been achieved. The advances in downstream technologies have benefited the vaccine industry enormously as purifying vaccine candidates to achieve consistent purity and quality in a timely manner is an integral part of the vaccine product development process. Case studies will be presented to illustrate how advances in purification technologies have facilitated vaccine process development and moved candidates faster to clinical evaluations.

2:45 Using Interaction Proteomics to Identify Novel Signaling Components Relevant for Cancer

Alexey VeraksaAlexey Veraksa, Ph.D., Associate Professor, Biology, University of Massachusetts, Boston

We are interested in the structure and function of signaling networks that control cell proliferation and differentiation, and in the mechanisms that cause aberrant signaling through these networks in disease. We interrogate signaling pathways using interaction proteomics, in particular, affinity purification-mass spectrometry (AP-MS). When applied to cancer-relevant pathways, such as Notch, RTK/ERK, and Hippo, our approaches have identified novel interactions that control these signaling networks under normal and pathological conditions.

3:15 Presentation to be Announced

3:30 Sponsored Presentation (Opportunity Available)

3:45 Refreshment Break in the Exhibit Hall with Poster Viewing

PURIFYING MEMBRANE PROTEINS

4:30 New Chemical Tools for Stabilization of Membrane Proteins

Qinghai ZhangQinghai Zhang, Ph.D., Associate Professor, Integral Structural and Computational Biology, The Scripps Research Institute

Integral membrane proteins comprise about a third of proteins encoded in genomes and more than half FAD-approved drug targets. The hydrophobic nature of membrane proteins requires their solubilization as isolated stable and functional particles but also presents a challenge for many biochemical and biophysical studies. We will present new chemical tool development that enhances the stability of membrane proteins and enables successful structural determinations.

5:00 Solving the Challenges of Membrane Proteins through Nanotechnology

Stephen SligarStephen G. Sligar, Ph.D., Director, Swanlund Endowed Chair, Molecular and Cellular Biology, The University of Illinois

Membrane proteins are involved in numerous vital biological processes, including transport, signal transduction and the enzymes in a variety of metabolic pathways. Unfortunately, membrane proteins are inherently recalcitrant to study using the normal toolkit available to scientists. The Nanodisc platform circumvents these challenges by providing a self-assembled system that renders typically insoluble, yet biologically and pharmacologically significant, targets such as receptors, transporters, enzymes, and viral antigens soluble in aqueous media.

5:30 Close of Day

5:30 - 5:45 Short Course Registration

5:45 - 8:45 Dinner Short Courses*

* Separate registration required


WEDNESDAY, JANUARY 11

8:00 am Conference Registration and Morning Coffee

BEAD-BASED PURIFICATION

8:30 Chairperson’s Remarks

Christopher Gray, Ph.D., Structural Biology Team Leader, Drug Discovery Program, CRUK Beatson Institute

8:35 Magnetic Beads for Antibody Purification

Ray Low, Ph.D., Scientist, Biologics Optimization, Amgen

Current linear chromatography technologies take relatively long purification processing time from CM to purified protein. I will talk about how, using the magnetic beads with some basic tools, the processing time can be radically reduced. The product quality, processing speed and recovery parameters comparing to the traditional column based chromatography will also be discussed.

9:05 Core Bead Chromatography for Preparation of Highly Pure, Infectious Respiratory Syncytial Virus in the Negative Purification Mode

Sophia T. Mundle, Ph.D., Deputy Director, Protein Chemistry, Sanofi Pasteur

Respiratory syncytial virus (RSV) is an important human pathogen, and a frequent viral cause of respiratory disease in infants, the elderly and immunocompromised. The overall disease burden warrants the development of a safe and effective prophylactic vaccine. One approach to vaccination against viral pathogens is the live-attenuated virus. The data which will be presented describe a scalable, chromatography-based purification procedure for preparation of highly pure, infectious live-attenuated RSV.

9:35 Sponsored Presentation (Opportunity Available)

10:05 Coffee Break in the Exhibit Hall with Poster Viewing

COMPUTATIONAL & MODULAR PROCESSES

10:50 Modular Approaches for Complex Therapeutic Molecules: Reinventing Smart Bioprocessing

Stefan SchmidtStefan R. Schmidt, Ph.D., MBA, Vice President, Rentschler Biotechnology

Our concept relies on the intelligent deconvolution of general purification issues in manageable chunks that are systematically rearranged to form a logical sequence of minimally required steps to achieve the intended quality and purity profile. Multiple modules are then assembled for each new molecule to redesign a quasi-platform downstream process. I will present the current status of our modular approach to transfer well-proven elements from platforms into downstream processes.

11:20 Case Study: Protease-Resistant Peptides for Protein Purification from Animal Plasma

Stefano MenegattiStefano Menegatti, Ph.D., Assistant Professor, Chemical and Biomolecular Engineering, North Carolina State University

Our goal is to develop synthetic peptide ligands with high biochemical stability and selectivity for protein purification from animal sera. To this end, we have devised a combined computational/experimental framework for generating variants of peptide ligands using non-natural amino acids. Initially, variants of antibody-binding sequences were designed and selected in silico. Our results strongly support the use of non-natural amino acids for designing peptide ligands with enhanced biorecognition and proteolytic stability.

11:50 Bespoke Bacterial Expression Vectors and Automated 3-Dimensional Lab Scale Purification Increases Throughput and Capacity in a Drug Discovery Protein Production Facility

Christopher GrayChristopher Gray, Ph.D., Structural Biology Team Leader, Drug Discovery Program, CRUK Beatson Institute

The protein production section of the Beatson Drug Discovery Program supplies a considerable number of highly purified and active recombinant proteins for structural biology, biophysical and biochemistry applications. In order to minimize any bottleneck, we have devised a series of bespoke in-house bacterial expression vectors that allow the production of proteins with multiple, protease cleavable, affinity and/or solubilizing tags resulting in parallel purification of numerous proteins with minimal operator intervention.

12:20 pm Sponsored Presentation (Opportunity Available)

12:50 Session Break

1:00 Luncheon Presentation (Sponsorship Opportunity Available) or Enjoy Lunch on Your Own

INNOVATING PURIFICATION PROCESSES

2:00 Chairperson’s Remarks

Stefan R. Schmidt, Ph.D., MBA, Vice President, Rentschler Biotechnology

2:05 Overload vs. Bind and Elute Cation Exchange Chromatography: A Case Study

David GloverDavid Glover, Engineer II, Purification Development, Genentech

An alternative purification approach, overload cation-exchange chromatography, has been shown to have the potential to match the impurity removal capabilities of operating in bind and elute mode while expanding the window of operation. This talk will discuss the two operation cation-exchange chromatography modes and focus on a case study comparing and contrasting the benefits and drawbacks from both a process design and manufacturing perspective.

2:35 An Affinity Chromatography Method for Antibody Purification via Nucleotide Binding Site Targeting Ligand

Basar BilgicerBasar Bilgicer, Ph.D., Associate Professor, Chemical and Biomolecular Engineering, University of Notre Dame

This talk describes a novel affinity chromatography technique that utilizes a small ligand that targets the nucleotide-binding site (NBS) located on Fab domain for the purification of antibodies from complex protein mixtures such as cell culture media and ascites fluids. Results of this study established in two different solid support applications, provided high levels of antibody recovery (>98%) and purity (>98%), and yielded reproducible chromatograms maintaining column stability over multiple injections.

3:05 Purification of Viral Particles

Yingxia Wen, Ph.D., Director and Head, Protein Biochemistry, Research, Seqirus, a CSL Company

3:35 Refreshment Break in the Exhibit Hall with Poster Viewing

4:30 The RAS Initiative at the Frederick National Lab: Producing RAS and RAS-Binding Proteins for Structural Biology, Biochemistry, and Assay Development

William GilletteWilliam Gillette, Ph.D., Principal Scientist, RAS Protein Production, and Deputy Director, Protein Expression Laboratory, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research (FNL)

Producing proteins for experiments in XRAY crystallography, NMR, SPR, assay development, CryoEM, biochemistry, tethered by layers, and neutron scattering platforms, the RAS Initiative is working closely with a large collection of internal and external groups to help advance knowledge on the structurally and biochemical properties of KRAS and its binding partners. My talk will review our progress and continuing challenges by presenting primary purification data and downstream application data.

5:00 Scaling-Up of a Downstream Purification Process for a New Recombinant Product (Nuwiq)

Martin LinhultMartin Linhult, Ph.D., Head, Bio100 Line 1, Biopharmaceuticals, Octapharma

Octapharma has developed a new process for the production of a recombinant human FVIII product derived from a human cell line (HEK293F cells). Clinical trials are ongoing with positive results. During process development, several different approaches have been tested, old established techniques as well as new ones have been evaluated. In this presentation, I will discuss scale-up of a new downstream purification process and also different affinity ligands that could be applied.

Buzz Sessions5:35 BuzZ Session B

Join your peers and colleagues for interactive roundtable discussions.

6:20 - 7:20 Reception in the Exhibit Hall with Poster Viewing

7:20 Close of Conference