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How to Achieve Higher Sensitivity with Hybrid Immunoaffinity LC-MS Assays

Jan 10, 2017 | Biopharma, Blogs | 0 comments

Protein-based biotherapeutics, including monoclonal antibodies (mAbs) and antibody-drug conjugates (ADCs) are a growing component of pharmaceutical companies’ drug pipelines. The growth of ADCs in particular is due to their ability to selectivity target and deliver a potent molecule to a cancer cell based on a specific tumor marker. In order to support this growing class of new drug molecules, robust and reliable bioanalytical methods are required. While ligand binding assays (LBAs) like ELISA have been the most popular platform for biotherapeutic quantitation, bioanalytical scientists have been increasingly adopting hybrid LBA/LC-MS methods in this area.

The strengths of hybrid LC-MS assays for this application include:

  • Selectivity
  • Broad Linear Dynamic Range (LDR)
  • The ability to multiplex a second analyte or catabolite
  • The quick method development time afforded by a generic method

For a bioanalytical scientist inexperienced in hybrid LBA/LC-MS signature peptide quantitation, the various workflows can appear complex and difficult. BioBA sample preparation kits are designed to make this complex process simple by enabling a magnetic bead-based approach to immunoaffinity sample preparation and providing all the reagents necessary (buffers, reagents, enzyme and bead) to complete the workflow.

Most ADCs are heterogeneous mixtures of species and an example is ado-trastuzumab emtansine, a lysine-linked ADC that is an approved treatment for patients with Her2+ breast cancer. The nature of the chemistry involved in lysine conjugation makes the drug product a heterogeneous mixture of species with a drug to antibody (DAR) of 0 to 8. The heterogeneous character of ADCs like adotrastuzumab emtansine require several bioanalytical assays during the drug development process. Some of these include:

  • Unconjugated payload
  • Conjugated antibody (DAR 1 to 8)
  • Total antibody (DAR 0 to 8)

Hybrid LBA/LC-MS assays can be used to address conjugated and total antibody assays by choosing an appropriate immunocapture reagent. An anti-payload antibody can be used to immunopurify and assay conjugated ADC species. To assay the total antibody, a generic anti-human Fc antibody can be employed for immunocapture, or a target-specific immunocapture strategy can be employed with recombinant target protein or an anti-idiotype antibody.

Download the tech note to see a full demonstration of a total antibody assay of ado-trastuzumab emtansine using hybrid LBA/LC-MS approach employing the BioBA sample preparation kit and a generic immunocapture strategy.

A 2-fold revolution: MS approaches for the bioanalysis of oligonucleotide therapeutics

In 1998, the US Food and Drug Administration (FDA) approved fomivirsen as the first therapeutic oligonucleotide therapeutic. This approval marked a revolution of mechanism of action discovered decades before finally coming to fruition. Since then, the landscape of chemical modifications of oligonucleotides, conjugations and formulations has evolved tremendously, contributing to improvements in stability, efficacy and safety. Today, more than a dozen antisense oligonucleotides (ASOs) and small interfering RNA (siRNA) drugs are on the market, most of which are designated as orphan drugs for treating rare genetic diseases.

Is “right first time, every time” a pipedream for metabolite identification by LC-MS?

If we lived in an ideal world, it would be possible to unambiguously identify metabolites using a single analytical experiment. This analytical technique would need to be efficient and easily generate the information needed from a routine assay that is also robust, enabling confident decision-making during drug discovery.

Supporting new CRISPR gene editing systems

Prime editing (PE) is a next-generation gene editing technology that utilizes a Cas9 protein fused to a prime editing guide ribonucleic acid (pegRNA) to achieve high CRISPR/Cas9 editing efficiency and precision. However, the length requirement of pegRNAs at 120–250 nucleotides (nt) and their high level of secondary structure formation present analytical challenges for the purity analysis of chemically synthesized pegRNAs during development and quality control (QC).

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