Optimized enzymatic cell lysis protocols for single-cell genomic analysis

Optimizing cell lysis is essential for reliable single-cell genomic analysis. This study sought to refine enzymatic lysis conditions to minimize incubation time while maintaining DNA integrity. Microdissected human leukocytes were digested with proteinase K under various incubation durations (2-16 h) and temperatures (37-60 °C), and genomic DNA recovery was assessed through Y-chromosome-specific PCR amplification. Shorter incubation periods combined with elevated temperatures, particularly at 60 °C, achieved amplification efficiencies comparable to or greater than those obtained with the conventional overnight digestion at 37 °C. Statistical analysis revealed no significant differences between the optimized and standard conditions. These results indicate that enzymatic lysis duration can be substantially reduced without compromising DNA yield or quality. The proposed approach enables same-day genomic preamplification and enhances the throughput of single-cell workflows, offering practical advantages for clinical diagnostics and forensic genetics.

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Publication Details

Journal
Cellular and Molecular Biology
Published
2026-02-13
DOI
https://doi.org/10.14715/cmb/2025.72.1.5
Primary Topic
Single-cell and spatial transcriptomics
Type
article
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article

Optimized enzymatic cell lysis protocols for single-cell genomic analysis

Hussein Mouawia, Houssam Raad, Hassan Ayoub, Ahmad Al Saabi et al.
Cellular and Molecular Biology
Single-cell and spatial transcriptomics
article

Optimized enzymatic cell lysis protocols for single-cell genomic analysis

Hussein Mouawia, Houssam Raad, Hassan Ayoub, Ahmad Al Saabi, Hamid Bou Saab
article en

Abstract

Optimizing cell lysis is essential for reliable single-cell genomic analysis. This study sought to refine enzymatic lysis conditions to minimize incubation time while maintaining DNA integrity. Microdissected human leukocytes were digested with proteinase K under various incubation durations (2-16 h) and temperatures (37-60 °C), and genomic DNA recovery was assessed through Y-chromosome-specific PCR amplification. Shorter incubation periods combined with elevated temperatures, particularly at 60 °C, achieved amplification efficiencies comparable to or greater than those obtained with the conventional overnight digestion at 37 °C. Statistical analysis revealed no significant differences between the optimized and standard conditions. These results indicate that enzymatic lysis duration can be substantially reduced without compromising DNA yield or quality. The proposed approach enables same-day genomic preamplification and enhances the throughput of single-cell workflows, offering practical advantages for clinical diagnostics and forensic genetics.

Cellular and Molecular BiologyVol. 72(1)
Lebanese University (LB), Rafik Hariri University Hospital (LB)
Zero hunger
Openalex Percentile: Top 57%
Single-cell and spatial transcriptomics
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Optimized enzymatic cell lysis protocols for single-cell genomic analysis — Hussein Mouawia, Houssam Raad, et al. · Cellular and Molecular Biology (2026) | TGRS Research Map | TGRS