Synonym |
YIGSR amide |
Species |
Human |
Protein Accession |
P01375 |
Purity |
Greater than 95% as determined by SDS-PAGE |
Endotoxin Level |
Less than 1.0 EU per µg of the protein |
Biological Activity |
The ED50 for this effect is typically 1-5 µg/mL |
Expression System |
E. coli |
Fusion Tag |
None |
Predicted Molecular Mass |
1 kDa |
Formulation |
Lyophilized from a 0.2 µm filtered solution of 20 mM Tris, 500 mM NaCl, pH 8.0 |
Reconstitution |
It is recommended to reconstitute the lyophilized YIGSR amide in sterile 18 MΩ-cm H2O not less
than 100 µg/ml, which can then be further diluted to other aqueous solutions. |
Storage & Stability |
Store lyophilized protein at -20°C. Aliquot the product after reconstitution to avoid repeated
freeze-thaw cycles. For long-term storage, the product should be stored at -70°C. |
FAQ
What is YIGSR amide, and how is it used in scientific research?
YIGSR amide is a synthetic peptide
derivative of a sequence from laminin, a key extracellular matrix glycoprotein. Laminin plays a crucial
role in cell adhesion, growth, migration, and differentiation. The peptide sequence YIGSR
(Tyr-Ile-Gly-Ser-Arg) is particularly noted for mediating cell attachment and signaling. YIGSR amide is
used in various scientific research areas due to its capacity to influence cellular behavior.
Researchers utilize this peptide in studies involving tissue engineering, regenerative medicine, and
cancer research, appreciating its ability to promote cell adhesion and migration. In tissue engineering,
YIGSR amide is often used to modify surfaces to create biomimetic environments conducive to cell
attachment. This ensures that cells can effectively adhere and grow on scaffolds designed for tissue
regeneration. Studies have demonstrated that coating biomaterials with YIGSR amide enhances cellular
integration and can play a pivotal role in the success of implants and engineered tissues. In
regenerative medicine, YIGSR amide has been explored for its ability to support stem cell
differentiation and proliferation. This is critical in the development of therapies aimed at repairing
or replacing damaged tissues. Researchers have been exploring its effect on various types of stem cells,
including mesenchymal and neural stem cells, hoping to guide their differentiation into specific
lineages necessary for therapeutic applications. Furthermore, in cancer research, YIGSR amide has been
studied for its potential to interfere with cancer cell adhesion—a critical step in metastasis. By
impeding the interaction of cancer cells with laminin, YIGSR amide might hinder the spread of cancer
cells, offering a potential strategy for combating cancer metastasis. Researchers employ various assays
and models, ranging from in vitro cell cultures to in vivo animal studies, to elucidate the peptide’s
effects and gather insights on its therapeutic potential. Overall, YIGSR amide serves as a versatile
tool in scientific research, with its applications extending to the modification of biomaterials, the
promotion of tissue regeneration, and the exploration of anti-metastatic strategies.
How does
YIGSR amide facilitate cell adhesion and what implications does this have?
YIGSR amide facilitates
cell adhesion through its interaction with laminin receptors on the surfaces of cells. The YIGSR
sequence is recognized by integrins and non-integrin laminin receptors, facilitating a robust adhesion
between the cells and the extracellular matrix. This interaction mimics natural laminin-mediated
adhesion, which is a fundamental process in maintaining tissue structure and function. The enhanced cell
adhesion mediated by YIGSR amide has profound implications in the biomedical field. In tissue
engineering, this feature is harnessed to improve the integration of cells with scaffolds, thereby
enhancing the development of bioengineered tissues. Typically, tissues are cultured on biomaterial
scaffolds that mimic the extracellular matrix, providing structural support for growing cells. YIGSR
amide, when incorporated into or applied onto these scaffolds, significantly enhances cellular
adherence, promoting cell proliferation and viability. This results in more robust tissue constructs,
with potential applications in skin, cartilage, and bone regeneration. In wound healing, YIGSR amide’s
ability to promote cell adhesion is similarly beneficial. It can enhance the migration of keratinocytes
and fibroblasts—cells critical to the repair of skin—into wound sites. This property speeds up the
re-epithelialization process, leading to quicker wound closure and reduced scarring. For this reason,
YIGSR amide is being explored in the development of advanced wound dressings. Moreover, in the context
of cell culture systems, YIGSR amide-coated surfaces offer improved adherence of cells, particularly
those that are difficult to maintain under typical culture conditions. This has led to more reliable
experimental outcomes, especially when studying primary cells or delicate cell lines. The controlled
interaction of YIGSR amide with cells also allows researchers to design targeted studies investigating
cell behavior in response to specific stimuli. Each application relies on YIGSR amide’s ability to
emulate natural cell-matrix interactions, making it indispensable in efforts to design more effective
biomedical devices and treatments. By optimizing cell adhesion, YIGSR amide-based methods open new
avenues for bioengineering and medical research.
In what ways can YIGSR amide impact cancer
treatment strategies?
YIGSR amide has the potential to influence cancer treatment strategies by
interfering with the adhesion and migration of cancer cells—crucial steps in the metastatic process.
Metastasis involves the spread of cancer cells from the primary tumor to distant locations, often
facilitated by interactions with the extracellular matrix components such as laminin. The YIGSR sequence
of laminin is integral to these interactions. By binding to laminin receptors on cancer cells, YIGSR
amide can inhibit these interactions, potentially reducing the metastatic spread of cancers. This
inhibitory action has made YIGSR amide a focus for researchers developing anti-metastatic therapies. By
blocking key adhesion sites on cancer cells, YIGSR amide may prevent their detachment from the primary
tumor and subsequent attachment to secondary sites, common steps in the metastatic cascade. These
properties have been explored in various in vitro and in vivo studies to assess the peptide’s efficacy
in preventing metastasis, particularly in aggressive cancers such as melanoma and certain carcinomas.
Additionally, research is investigating the use of YIGSR amide in combination with other cancer
therapies. It is postulated that deploying YIGSR amide alongside chemotherapy or radiotherapy could
amplify the overall therapeutic effect. While chemotherapeutic agents target rapidly dividing cells,
YIGSR amide could concurrently prevent surviving cancer cells from migrating and establishing new
tumors. This combined approach may prove more effective than traditional methods, leading to improved
patient outcomes. In a similar vein, YIGSR amide might be paired with nanotechnology-based delivery
systems to target tumors more precisely, reducing off-target drug effects and enhancing anti-cancer
efficacy. This targeted strategy also minimizes the side effects often associated with cancer treatment,
potentially improving patient quality of life. Furthermore, YIGSR amide's ability to mimic natural
physiological processes makes it a promising candidate for incorporation into cancer vaccines or
immunotherapies. These therapies often require precise interactions at the cellular level to be
effective, and YIGSR amide can support these processes. Researchers continue to study its mechanisms to
better understand how it can be harnessed to improve existing cancer treatment paradigms and develop
novel therapeutic pathways.
Can YIGSR amide play a role in drug delivery systems, and if so, how?
YIGSR amide can indeed play a critical role in the development of targeted drug delivery systems.
The peptide’s unique ability to bind to laminin receptors, which are prevalent on certain cell types,
enables it to direct therapeutic agents specifically to these cells. This receptor-targeted approach is
particularly advantageous in drug delivery, where precision is crucial to maximize therapeutic benefits
while minimizing side effects. In the realm of nanotechnology, YIGSR amide is used to functionalize
nanoparticles—notably liposomes and polymeric nanoparticles—creating a surface that interacts
specifically with target cells. By conjugating YIGSR amide to drug-loaded nanoparticles, researchers can
exploit its affinity for laminin receptors to preferentially direct the nanoparticles to particular
cells. This is especially applicable in the targeted treatment of diseases such as cancer or conditions
involving specific tissues, like the central nervous system. The resulting increases in drug
concentration at the target site increase the therapeutic efficacy and decrease systemic drug exposure,
reducing harmful side effects typically associated with conventional drug administration methods.
Moreover, the peptide can support the development of multi-functional drug delivery systems that
integrate diagnostics and therapeutics, commonly referred to as theranostics. By delivering therapeutic
agents and contrast materials or imaging probes concurrently, these systems can monitor treatment
efficacy in real-time, providing valuable feedback to clinicians. Researchers are also investigating the
possibility of embedding YIGSR amide within hydrogel matrices to develop controlled-release drug
delivery platforms. This method is particularly appealing for localized therapy, where sustained release
of the drug is desired to maintain therapeutic levels over prolonged periods without the need for
frequent administration. This not only improves patient compliance but also ensures a consistent
therapeutic effect. Furthermore, the peptide’s modulation of cellular interactions renders it a valuable
tool in designing biomaterials for drug delivery, which must often interact harmoniously with the
biological environment. Its role in enhancing cell-material interactions helps improve the
biocompatibility and functionality of these materials. Overall, the integration of YIGSR amide into drug
delivery systems exemplifies a powerful strategy to leverage modern advances in peptide engineering and
materials science, offering promising improvements in the delivery and efficacy of therapeutic
agents.
What are the broader implications of using YIGSR amide in regenerative medicine?
In
regenerative medicine, the use of YIGSR amide has far-reaching implications, predominantly due to its
role in modulating cellular interactions and promoting tissue regeneration. Regenerative medicine aims
to repair or replace damaged tissues and organs, utilizing the body's inherent repair mechanisms. YIGSR
amide facilitates this by enhancing cell adhesion, migration, and proliferation, critical processes in
tissue repair and regeneration. An important application of YIGSR amide in regenerative medicine is in
the enhancement of scaffold-based tissue engineering strategies. It has been found that coating or
integrating scaffolds with YIGSR amide enhances the scaffolds’ ability to support cell adhesion and
proliferation, two fundamental processes for successful tissue regeneration. This modification makes
scaffolds more akin to the natural extracellular matrix, offering a conducive environment for the cells
to proliferate and differentiate. As such, scaffolds modified with YIGSR amide are used in the
engineering of various tissues, from bone and cartilage to skin and neural tissues. In stem cell
therapy, YIGSR amide’s influence on cellular behavior has significant implications as well. It supports
the differentiation of stem cells, which is crucial for repairing specific tissues. By guiding stem
cells to become specific cell types, YIGSR amide enhances the potential for developing targeted
therapies for diseases and injuries where specific cell loss or dysfunction is involved. Furthermore,
the ability of YIGSR amide to enhance wound healing processes is noteworthy. The peptide promotes the
migration of key cell types involved in wound repair, such as keratinocytes and fibroblasts, to
accelerate healing. This application is particularly relevant to chronic wounds, common in conditions
such as diabetes, where impaired healing is a significant issue. Enhanced wound healing strategies
leveraging YIGSR amide could lead to faster recovery times and potentially reduced healthcare costs
associated with long-term wound care. YIGSR amide also holds promise in the development of bioactive
coatings for implants and medical devices. Coating these devices with YIGSR amide could enhance their
integration into surrounding tissues, minimizing immune rejection and improving device longevity and
performance. Ultimately, the implications of YIGSR amide in regenerative medicine encompass not only
improved strategies for tissue engineering and stem cell therapies but also novel approaches to
accelerate healing and enhance the performance of medical devices. Through these diverse applications,
YIGSR amide continues to demonstrate its wide-ranging utility in advancing the field of regenerative
medicine.