Biotin-Ahx-LPETGS-NH2 Substrate: A Versatile Tool for Protease Activity Studies

LPETGS
LIPTSTIC mechanism, from the cited paper.

The study of protease activity is critical for understanding cellular processes, disease mechanisms, and drug development. Among the various tools available for protease research, the Biotin-Ahx-LPETGS-NH2 substrate has emerged as a highly specific and versatile reagent. This peptide substrate is designed to detect and quantify the activity of sortase A, an enzyme widely used in protein engineering and bioconjugation. In this article, we explore the structure, applications, and significance of the Biotin-Ahx-LPETGS-NH2 substrate.


Key Takeaways

  • Biotin-Ahx-LPETGS-NH2 is a peptide substrate specifically designed for sortase A activity assays.
  • The substrate features a biotin tag for easy detection and purification, an Ahx (6-aminohexanoic acid) spacer for flexibility, and the LPETGS recognition sequence for sortase A.
  • It is widely used in protein labelingsite-specific protein modification, and enzyme kinetics studies.
  • The substrate’s design enables high sensitivity and specificity in detecting sortase A activity.
  • Applications include bioconjugationlive-cell imaging, and drug discovery.

Structure and Design of Biotin-Ahx-LPETGS-NH2

Biotin Tag for Detection and Purification

The biotin tag in the Biotin-Ahx-LPETGS-NH2 substrate serves as a universal handle for detection and purification. Biotin’s strong affinity for streptavidin allows for efficient immobilization on solid supports or visualization using streptavidin-conjugated fluorophores. This feature is particularly useful in ELISAWestern blotting, and pull-down assays, where the substrate’s interaction with sortase A can be easily monitored.

Ahx Spacer for Enhanced Flexibility

The inclusion of an Ahx (6-aminohexanoic acid) spacer between the biotin tag and the LPETGS sequence provides structural flexibility. This spacer ensures that the biotin tag does not sterically hinder the interaction between the substrate and sortase A, thereby maintaining high enzymatic efficiency. Additionally, the Ahx spacer improves the solubility of the peptide, making it suitable for a wide range of experimental conditions.

LPETGS Recognition Sequence

The LPETGS sequence is the core recognition motif for sortase A, a transpeptidase enzyme derived from Staphylococcus aureus. Sortase A cleaves the peptide bond between the threonine (T) and glycine (G) residues, enabling the attachment of functional groups or proteins to the C-terminus of the substrate. This sequence-specific cleavage is the basis for the substrate’s high specificity in sortase A activity assays.

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LPETGS

Applications of Biotin-Ahx-LPETGS-NH2

Protein Labeling and Bioconjugation

One of the primary applications of the Biotin-Ahx-LPETGS-NH2 substrate is in protein labeling and bioconjugation. Sortase A-mediated reactions allow for the site-specific attachment of labels, such as fluorophores or affinity tags, to proteins of interest. This approach is widely used in antibody-drug conjugates (ADCs)fluorescent protein tagging, and surface immobilization for biosensors.

Enzyme Kinetics Studies

The substrate is also employed in enzyme kinetics studies to characterize the activity and specificity of sortase A. By monitoring the cleavage of the LPETGS sequence, researchers can determine kinetic parameters such as Km and kcat. These studies provide valuable insights into the catalytic mechanism of sortase A and its potential applications in protein engineering.

Live-Cell Imaging

In live-cell imaging, the Biotin-Ahx-LPETGS-NH2 substrate can be used to visualize protease activity in real-time. The biotin tag allows for the incorporation of fluorescent probes, enabling the detection of sortase A activity in living cells. This application is particularly useful for studying cell surface dynamics and protein-protein interactions in their native environment.


Advantages of Biotin-Ahx-LPETGS-NH2

High Sensitivity and Specificity

The Biotin-Ahx-LPETGS-NH2 substrate offers high sensitivity and specificity for sortase A, making it an ideal tool for detecting low levels of enzyme activity. The LPETGS sequence ensures that the substrate is exclusively cleaved by sortase A, minimizing off-target effects.

Versatility in Experimental Design

The substrate’s modular design allows for customization to suit specific experimental needs. For example, the biotin tag can be replaced with other affinity tags or fluorophores, depending on the application. This versatility makes the substrate a valuable reagent in both basic research and industrial applications.

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Compatibility with High-Throughput Assays

The Biotin-Ahx-LPETGS-NH2 substrate is compatible with high-throughput screening (HTS) platforms, enabling the rapid identification of sortase A inhibitors or activators. This capability is particularly relevant in drug discovery, where the substrate can be used to screen large compound libraries for potential therapeutic agents.

Pasqual, G., Chudnovskiy, A., Tas, J. et al. Monitoring T cell–dendritic cell interactions in vivo by intercellular enzymatic labelling. Nature 553, 496–500 (2018). https://doi.org/10.1038/nature25442

Unnatural Amino Acids: Citrulline

Citrulline, an unnatural amino acid, is a non-proteinogenic amino acid that plays a significant role in the urea cycle and nitric oxide production. Unlike proteinogenic amino acids, citrulline is not directly encoded by DNA but is synthesized through metabolic pathways. This article explores the properties, synthesis, and applications of citrulline, with insights from LifeTein’s expertise in custom peptide synthesis.

Key Takeaways

  • Non-Proteinogenic Amino Acid: Citrulline is not encoded by DNA but plays a crucial role in the urea cycle.

  • Metabolic Intermediate: Acts as an intermediate in the urea cycle, converting ammonia into urea.

  • Nitric Oxide Production: Involved in the production of nitric oxide, which helps in vasodilation.

  • LifeTein Expertise: LifeTein offers custom synthesis of citrulline-containing peptides for research purposes.


Properties of Citrulline

Chemical Structure

Citrulline, also known as 2-amino-5-(carbamoylamino)pentanoic acid, has a molecular formula of C6H13N3O3. It is a white crystalline powder that is soluble in water.

Role in the Urea Cycle

Citrulline is a key intermediate in the urea cycle, which is the primary pathway for the removal of ammonia in mammals. The cycle converts toxic ammonia into urea, which is then excreted in urine.

Nitric Oxide Production

Citrulline is also involved in the production of nitric oxide (NO), a molecule that plays a crucial role in vasodilation and blood flow regulation. The conversion of citrulline to arginine, catalyzed by nitric oxide synthase (NOS), is a critical step in NO production.

Synthesis of Citrulline

Biosynthesis

Citrulline is synthesized from ornithine and carbamoyl phosphate in a reaction catalyzed by the enzyme ornithine transcarbamylase. This reaction is a central step in the urea cycle.

Chemical Synthesis

Citrulline can also be synthesized chemically through various methods, including the reaction of asymmetric dimethylarginine (ADMA) with dimethylarginine deiminase (DDAH). This synthetic approach is used for producing citrulline for research and therapeutic purposes.

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Citrulline

Applications of Citrulline

Medical and Therapeutic Uses

Citrulline is used in medical research to study metabolic disorders and cardiovascular diseases. Its role in the urea cycle makes it a potential therapeutic agent for conditions related to ammonia toxicity.

Sports and Exercise

Citrulline is popular among athletes and bodybuilders due to its potential to enhance blood flow and improve exercise performance. Supplements containing citrulline are marketed for their ability to boost nitric oxide production and reduce muscle fatigue.

Research Applications

LifeTein offers custom peptide synthesis services, including the incorporation of citrulline into peptides for research purposes. Researchers can utilize citrulline-containing peptides to study various biological processes and develop new therapeutic strategies.

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Future Directions

Advancements in Synthesis Techniques

Ongoing research aims to develop more efficient and scalable methods for synthesizing citrulline and its derivatives. Innovations in chemical synthesis and biotechnological approaches are expected to enhance the availability and utility of citrulline in scientific research and therapeutics.

Expanding Applications

As the understanding of citrulline’s properties and applications grows, its use in various fields, including drug discovery and protein engineering, is likely to expand. LifeTein’s commitment to providing high-quality custom peptides will continue to support advancements in these areas.

FAQ

What Is Citrulline?

Citrulline is an unnatural amino acid that plays a crucial role in the urea cycle and nitric oxide production.

Why Is Citrulline Important?

Citrulline is important for its role in ammonia detoxification and nitric oxide production, which are essential for metabolic and cardiovascular health.