Sequence and structure-based tool for therapeutic antibody post-translational modifications (PTM) sites analysis, prediction and de-risking

Knowledge base of antibody humanization

Introduction of GeneMedi’s LIBRA OPTM™

Definition: What is antibody post-translational modifications (PTM)

Antibody post-translational modifications (PTM) sites and the therapeutic antibody developability.

How to de-risk the PTM site of your antibody? (The workflow)

How to use GeneMedi's OPTM™ tool

Step 1: Click HERE to use GeneMedi’s LIBRA OPTM™ tool

Step 2: Check antibody sequence (Mouse IgG only)

Step 3: Fill in the Antibody name, email and submit the form

Introduction of GeneMedi’s LIBRA OPTM™

GeneMedi’s LIBRA OPTM™ is a powerful optimization tool for antibody post-translational modifications (PTM) site de-risking. The LIBRA-OPTM combines sequence and structure-based in silico algorithm with antibody optimization for developing the therapeutic antibody based on post-translational modifications (PTM) site analysis, prediction and de-risking.

If you want Monoclonal antibody (mab) humanization service, please vist GeneMedi's LIBRA HuEasy™.

What is antibody post-translational modifications (PTM)

Post-translational modifications (PTM) refer to the modification of amino acid side chain of some proteins after biosynthesis. It is a covalent processing events, which change the properties of a protein by proteolytic cleavage and adding a modifying group, such as acetyl, phosphoryl, glycosyl and methyl, to one or more amino acids.

In recent years, the medical application of therapeutical monoclonal antibodies (mAbs) has been rapidly growing due to its targetability, low-immunogenicity, and good tolerance. It has become an important therapeutic agent for numerous diseases including cancer, autoimmune, and infectious diseases. During the therapeutical monoclonal antibody development, different physical and chemical factors influence PTM of antibody,which affect the stability, immunogenicity, and binding with target antigens.

Antibody post-translational modifications (PTM) sites and the therapeutic antibody developability

BLike all proteins, mAbs are susceptible to chemical degradation (e.g., oxidation) and enzymatic modifications (e.g., sulfation) during cell culture. Chemical and enzymatic modifications contribute to heterogeneity. For example, asparagine (Asn) deamidation could generate charge variants; tryptophan (Trp) oxidation could generate hydrophilic or hydrophobic variants. In addition, chemical modifications could affect the physical stability and biological activity of antibodies. For example, isomerization within the Fab region could reduce conformational stability, whereas deamidation within complementary-determining region (CDR) loops could reduce binding affinity.

How to de-risk the PTM site of your antibody? (The workflow)

Experimental approaches for identifying PTM liabilities are time-consuming and require high quantities of the purified protein. The sample preparation and data analysis for peptide mapping is incredibly labor intensive. At earlier stages of drug development, the number of forced degradation conditions is limited by the low availability of the purified protein. Therefore, computational tools are becoming more common during developability assessments due to the low cost, lack of sample consumption, and high speed. In the past decade, computational tools have been used to predict PTM liable sites and engineer antibodies with better chemical stability.

we focused on the common PTM of mAbs, and summarize their causes, modification sites, the influences on the mAbs’ physicochemical properties, biological activities, and stabilities, as well as the main analytical strategies, aiming to provide some references for the in-depth quality analysis of therapeutical mAbs.

Computational approaches for PTM prediction can be divided into three categories: 1. sequence-based, 2. structure-based, and 3. physics-based. Sequence-based approaches either flag individual residues prone to chemical degradation (e.g., methionine oxidation) or liable motifs (e.g., NG, NS, and NT for deamidation). Structure-based approaches predict PTM liabilities by using structural features correlated with enzymatic and chemical modifications. Common structural features include, but are not limited to, secondary structure, water coordination number (WCN), solvent-accessible surface area (SASA) and machine learning algorithms.

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