SOP Guide for Pharma

Biosimilars: SOP for Glycosylation Analysis in Clone Selection – V 2.0


Biosimilars: SOP for Glycosylation Analysis in Clone Selection – V 2.0


Standard Operating Procedure for Glycosylation Analysis in Biosimilar Clone Selection

Department Biosimilars
SOP No. SOP/BS/021/2025
Supersedes SOP/BS/021/2022
Page No. Page 1 of 15
Issue Date 04/05/2025
Effective Date 06/05/2025
Review Date 04/05/2026

1. Purpose

To define the procedure for analyzing glycosylation profiles of expressed biosimilar proteins in mammalian cell clones, facilitating clone selection based on critical quality attributes (CQAs).

2. Scope

This SOP applies to Analytical Development, Cell Line Development, and Quality Control teams involved in assessing glycan structures during biosimilar clone screening.

3. Responsibilities

4. Accountability

The Head of Analytical Development is accountable for ensuring accurate glycan profiling and interpretation to guide clone selection in biosimilar programs.

5. Procedure

5.1 Sample Preparation

  1. Collect 0.5–1.0 mg purified biosimilar protein from each clone.
  2. Buffer-exchange to PBS if required using desalting columns.
  3. Record sample details in Glycosylation Sample Log (Annexure-1).

5.2 N-linked Glycan Release

  1. Denature protein at 95°C for 10 minutes in presence of SDS and DTT.
  2. Add NP-40 and PNGase F enzyme; incubate at 37°C for 18 hours.

5.3 Glycan Labeling

  1. Dry released glycans using vacuum concentrator.
  2. Label with 2-AB (2-aminobenzamide) or procainamide dye in sodium cyanoborohydride solution.
  3. Incubate at 65°C for 2 hours in the dark.

5.4 HPLC/UPLC Analysis

  1. Inject labeled glycans onto amide column (e.g., BEH Glycan) connected to HPLC/UPLC system.
  2. Run with gradient of acetonitrile and ammonium formate buffer.
  3. Acquire fluorescence signal and calculate relative peak areas.

5.5 Optional Mass Spectrometry

  1. Desalt labeled glycans using HILIC cartridges.
  2. Analyze using LC-MS or MALDI-TOF to determine glycan composition.

5.6 Lectin Blotting (Optional)

  1. Run protein sample on SDS-PAGE and transfer to membrane.
  2. Block membrane and incubate with biotinylated lectins (e.g., SNA, ConA).
  3. Detect with streptavidin-HRP and chemiluminescent substrate.

5.7 Data Interpretation and Reporting

  1. Assign glycan peaks using reference ladder or glycan database.
  2. Calculate % abundance of high mannose, complex, sialylated, and fucosylated glycans.
  3. Compare profiles with innovator molecule specifications.
  4. Record results in Glycan Profile Log (Annexure-2).

6. Abbreviations

7. Documents

  1. Glycosylation Sample Log (Annexure-1)
  2. Glycan Profile Log (Annexure-2)

8. References

9. SOP Version

Version: 2.0

10. Approval Section

Prepared By Checked By Approved By
Signature
Date
Name
Designation
Department

11. Annexures

Annexure-1: Glycosylation Sample Log

Date Clone ID Sample Volume (µL) Protein Conc. (mg/mL) Operator
03/05/2025 CL-BS-021 500 2.0 Sunita Reddy

Annexure-2: Glycan Profile Log

Date Clone ID High Mannose (%) Fucosylated (%) Sialylated (%) Total Glycan Diversity Remarks
04/05/2025 CL-BS-021 12.5 82.1 5.4 8 major peaks Acceptable match with reference

Revision History:

Revision Date Revision No. Revision Details Reason for Revision Approved By
04/05/2025 2.0 Included LC-MS and lectin blot as optional methods Annual SOP review and method expansion
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