Obesity-related Therapeutic Target Identification Service
InquiryUnlocking Obesity Solutions Through Precision Target Discovery
Our obesity-related therapeutic target identification service at Protheragen leverages genetic, transcriptomic, and proteomic data to identify key molecular targets involved in obesity by integrating genome-wide association studies (GWAS), expression quantitative trait loci (eQTL), protein-protein interaction (PPI) networks, and drug-gene interaction databases, enabling the discovery of novel genes, pathways, and proteins that are modulated for therapeutic purposes, enhancing the efficacy of obesity treatments through drug development and repurposing.
At Protheragen, our obesity-related candidate gene identification service identifies novel genetic and molecular targets for obesity treatment by uncovering key genes and pathways involved in obesity development. In parallel, our obesity-related drug-gene interaction analysis service aids pharmaceutical companies in developing new drugs or repurposing existing ones by analyzing the interactions between these identified genes and potential therapeutic compounds.
Obesity-related Candidate Gene Identification Service
This service focuses on discovering genes that play critical roles in the development of obesity. This service employs advanced bioinformatics techniques such as GWAS to identify obesity-associated genetic variants and eQTL analysis to prioritize genes that influence gene expression. Additionally, PPI network analysis is used to map the interactions between obesity-related proteins, helping to identify key hub genes involved in critical pathways such as energy homeostasis, lipid metabolism, and inflammation.
Obesity-related Drug-Gene Interaction Analysis Service
This service examines how obesity-related genes identified through the candidate gene identification service interact with existing drugs, using drug-gene interaction databases such as the drug-gene interaction database (DGIdb). By evaluating known interactions between drugs and obesity-related genes, this service facilitates the identification of potential drugs that are repurposed to target obesity. Computational tools like molecular docking are used to predict how these drugs bind to obesity-related proteins, providing insights into their therapeutic efficacy.
Our service process begins with obesity-related candidate gene identification, where we analyze genetic data using advanced bioinformatics tools to identify key genes and pathways linked to obesity. Once the candidate genes are identified, the obesity-related drug-gene interaction analysis evaluates potential drug interactions by leveraging molecular docking simulations and drug-gene interaction databases. This dual approach ensures a thorough exploration of genetic targets and their therapeutic potential, providing pharmaceutical companies with actionable insights for drug development or repurposing and supporting the creation of personalized obesity treatments.
Data Acquisition and Integration
The process begins by acquiring genetic, transcriptomic, and proteomic data related to obesity from public databases (e.g., GWAS and eQTL studies).
Gene and Target Prioritization
GWAS and eQTL analysis prioritize obesity-associated genes, followed by PPI network construction to identify hub genes central to obesity's molecular mechanisms.
Drug-gene Interaction Analysis
Drug-gene interaction databases are queried to identify approved drugs that target obesity-related genes, facilitating drug repurposing efforts.
Validation and Reporting
Molecular docking simulations and pathway enrichment analyses validate the therapeutic potential of identified targets. A detailed report is generated, summarizing the findings and providing recommendations for potential drug targets and interventions.
Anti-Obesity Therapy Development
In addition to this, we provide a one-stop service for the development of anti-obesity therapies and conduct detailed preclinical studies.
Applications
- Identifying novel molecular targets for obesity facilitates the development of new drugs designed to modulate these targets, offering more effective treatments for obesity.
- By analyzing drug-gene interactions, this service helps in repurposing existing drugs that interact with obesity-related genes, accelerating the therapeutic discovery process.
- The service provides insights into individual genetic profiles, enabling the design of personalized therapies that target specific genes contributing to a patient's obesity.
- Pharmaceutical companies and researchers can utilize this service for preclinical studies to validate genetic targets and test potential therapeutic compounds.
Advantages
- The service integrates genetic, transcriptomic, and proteomic data, offering a complete view of obesity-related molecular mechanisms.
- By identifying and prioritizing key genes, pathways, and drug-gene interactions, this service enhances the precision and efficacy of drug development efforts.
- Leveraging in silico bioinformatics tools reduces the time and cost associated with traditional drug discovery methods.
- The integration of multiple data sources ensures the identification of the most relevant and actionable therapeutic targets.
Publication
Technology: Molecular docking, Molecular dynamics simulations, In vivo validation, X-ray crystallography data
Journal: International Journal of Molecular Sciences
IF: 4.9
Published: 2024
Results: This systematic review focused on identifying potential therapeutic targets for obesity using in silico methods, including molecular docking and molecular dynamics simulations, with subsequent in vivo validation. The study explored seven key therapeutic targets: leptin receptor (LEPR), protein tyrosine phosphatase 1B (PTP1B), fat mass and obesity-associated protein (FTO), human pancreatic lipase (HPL), type 1 cannabinoid receptor (CB1), CD36 receptor, and acetyl-CoA carboxylase (ACC). These targets were analyzed for their potential as therapeutic agents against obesity, with particular emphasis on their molecular mechanisms and interactions with bioactive compounds. Results from in vivo validations supported the efficacy of several identified compounds in reducing body weight, improving lipid profiles, and regulating metabolic pathways, particularly those involved in lipid metabolism and energy balance.
Fig.1 The general diagram of therapeutic targets for obesity studied in silico and reassessed in vivo, and possible metabolic effects of modulation. (de Medeiros, et al., 2024)
Frequently Asked Questions
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What is the purpose of the obesity-related therapeutic target identification service?
The purpose of the obesity-related therapeutic target identification service is to pinpoint critical genetic and molecular factors involved in obesity, supporting the creation of innovative drugs and tailored treatment strategies.
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What is the role of the drug-gene interaction analysis service?
This service evaluates the interactions between identified obesity-related genes and existing drugs, helping to repurpose approved drugs or guide the development of new therapies.
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How can this service support personalized medicine?
By identifying the specific genetic factors contributing to a patient's obesity, the service enables the design of tailored treatment plans that target these genes for more effective outcomes.
At Protheragen, our service provides a comprehensive solution for discovering and validating key genetic and molecular targets involved in obesity. By integrating advanced bioinformatics tools, including molecular docking, GWAS, and drug-gene interaction databases, Protheragen identifies novel therapeutic targets and evaluates existing drug interactions to facilitate new drug development and repurposing. Please feel free to contact us for more information about our services and anti-obesity solutions.
Reference
- de Medeiros, W.F.; et al. Anti-obesity therapeutic targets studied in silico and in vivo: A systematic review. International Journal of Molecular Sciences. 2024, 25(9): 4699. (CC BY 4.0)
All of our services and products are intended for preclinical research use only and cannot be used to diagnose, treat or manage patients.