An In Silico Method For Design Of Soluble Fusion Partner For Expression Of Modified Glucagon-Like Peptide-1 In E.coli BL21(DE3).

Glucagon-like peptide-1 (GLP-1) is an essential therapeutic agent for diabetes and obesity; however, its poor solubility presents significant challenges in production, leading to complex purification steps, increased processing time, and higher costs.This study introduces a novel strategy employing an in-silico approach to identify a soluble fusion partner (sfp) to enhance mGLP-1 solubility.Using Protein-sol tool, we identified a fusion partner that can be fused to mGLP-1 via a His6-EK linker resulted a solubility score of 0.947.The resulting fusion construct was cloned into the pET22b vector and expressed in Escherichia coli.Expression analysis revealed that the fusion partner effectively enhanced GLP-1 solubility, maintaining it across various IPTG concentrations.This approach offers a promising solution to simplify GLP-1 protein expression, potentially reducing purification complexity and manufacturing costs.These In-Silico method could also be applied for expression of other proteins and peptides.

Authors

Publication Details

Journal
African Journal of Biomedical Research
Published
2024-10-04
DOI
https://doi.org/10.53555/ajbr.v27i3s.2385
Primary Topic
Pancreatic function and diabetes
Type
article
Field-Weighted Citation Impact
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article

An In Silico Method For Design Of Soluble Fusion Partner For Expression Of Modified Glucagon-Like Peptide-1 In E.coli BL21(DE3).

Venkata Sri Krishna Kona
African Journal of Biomedical Research
Pancreatic function and diabetes
article

An In Silico Method For Design Of Soluble Fusion Partner For Expression Of Modified Glucagon-Like Peptide-1 In E.coli BL21(DE3).

Venkata Sri Krishna Kona
article en

Abstract

Glucagon-like peptide-1 (GLP-1) is an essential therapeutic agent for diabetes and obesity; however, its poor solubility presents significant challenges in production, leading to complex purification steps, increased processing time, and higher costs.This study introduces a novel strategy employing an in-silico approach to identify a soluble fusion partner (sfp) to enhance mGLP-1 solubility.Using Protein-sol tool, we identified a fusion partner that can be fused to mGLP-1 via a His6-EK linker resulted a solubility score of 0.947.The resulting fusion construct was cloned into the pET22b vector and expressed in Escherichia coli.Expression analysis revealed that the fusion partner effectively enhanced GLP-1 solubility, maintaining it across various IPTG concentrations.This approach offers a promising solution to simplify GLP-1 protein expression, potentially reducing purification complexity and manufacturing costs.These In-Silico method could also be applied for expression of other proteins and peptides.

African Journal of Biomedical Research
Openalex Percentile: Top 68%
Pancreatic function and diabetes
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