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Peptide mapping is a critical workflow in biotherapeutic protein characterization and is essential for elucidating the primary amino acid structure of proteins. For recombinant protein pharmaceuticals, such as monoclonal antibodies (mAbs) and antibody-drug conjugates (ADCs), peptide mapping is used for proof of identity, primary structural characterization and quality assurance/quality control (QA/QC). Global regulatory agencies, including US Food and Drug Administration (US FDA) and European Medicines Agency (EMA), look to harmonized guidelines from the International Council for Harmonisation (ICH). ICH Q6B covers the test procedures and acceptance criteria for biologic drug products, and specifies the use of peptide mapping as a critical quality test procedure for drug characterization used to confirm desired product structure for lot release purposes.
In order to generate a peptide map, the therapeutic protein must first be digested into its constituent peptides via a chemical or enzymatic reaction. Robust separation and identification of the resultant peptides then provides insight into a protein’s full sequence information; displaying each amino acid component and the surrounding amino acid microenvironment, including disulfide linkage information. Structural characterization at this level highlights post translational modifications (PTMs) such as site-specific glycosylation, amino acid substitutions (sequence variants) and/or truncations which may result from erroneous transcription of complementary DNA. Within a bioproduction environment, peptide mapping is necessary for manufacturing process monitoring and QC. It facilitates product comparability testing, which is necessary to identify any product-related impurities, such as deamidation and/or oxidation following any formulation, manufacturing process or storage change.
Due to its complexity and inherent variability, peptide mapping is generally performed in a comparative manner; for example, biosimilars would be compared to a reference or control substance, such as the innovator biologic, in a side-by-side experiment. An in-depth analysis is then required to identify minor and even isobaric differences in protein primary structure. The modern biopharmaceutical and protein research laboratory is tasked with providing high quality analytical results, often in high-throughput, regulated environments. Some technologies currently employed for biopharmaceutical peptide mapping are subject to high levels of irreproducibility, poor sensitivity, and high levels of time-consuming manual work—with protracted methodologies that are not amenable to automation and often require 24 hours to achieve full protein digestion.
This variability impacts data confidence. Moreover, it increases potential for introduction of non-product related artifacts during manual sample handling.
The most recent advances in protein sample preparation chemistries, ultra-high performance liquid chromatography (UHPLC), mass spectrometry (MS) hardware and intuitive software facilitate the generation of comprehensive, confident peptide maps.
Learn how to increase confidence in biopharma peptide mapping. In this series, four new technologies will be demonstrated that dramatically improve upon established mapping workflows.
Learn how to increase confidence in biopharma peptide mapping. In this series, four new technologies will be demonstrated that dramatically improve upon established mapping workflows.
Learn how to increase confidence in biopharma peptide mapping. In this series, four new technologies will be demonstrated that dramatically improve upon established mapping workflows.
Learn how to increase confidence in biopharma peptide mapping. In this series, four new technologies will be demonstrated that dramatically improve upon established mapping workflows.
Get information about the biopharmaceutical industry and why there is need for detailed structural insight of biologic medicines.
Peptide mapping is a critical biopharma characterization workflow. Discover the points of interest and tools needed on your journey in this handy infographic.
See how the latest analytical workflow solves the challenges of therapeutic protein characterization.
Combining the Thermo Scientific™ SMART Digest™ magnetic kits with the Thermo Scientific™ KingFisher™ Duo Prime purification system provides an automated approach to protein digest method optimization.
Combining the Thermo Scientific™ SMART Digest™ magnetic kits with the Thermo Scientific™ KingFisher™ Duo Prime purification system provides an automated approach to protein digest method optimization.
Two classic in-solution digestion approaches were compared to the recently developed SMART Digest kit method to quantify the extent of post-translational and chemical modifications of a therapeutic recombinant mAb, rituximab.
Join Dr Rowan Moore as she investigates alternatives to traditional in-solution protein digestion protocols for peptide mapping of biopharmaceuticals.
Learn about how the latest chromatography, mass spectrometry and software are accelerating confident decision making at Alexion Pharmaceuticals, Inc.
Stephane Houel, Biopharma Product Marketing Specialist, describes a high throughput peptide mapping workflow using the Thermo Scientific Vanquish UHPLC system and Thermo Scientific Q Exactive HF mass spectrometer.
Optimize your protein digestion protocol; discover the Thermo Scientific SMART Digest Kits for fast, simple and reproducible peptide mapping.
Get faster, easier and more reproducible results from your samples in just three easy steps.
NIBRT Application note overview detailing development of a robust and reproducible, high-precision, automated, peptide mapping workflow for LC and LC-MS