Synonym |
IGF-I (30-41), IGF-I C-Peptide |
Species |
Human |
Protein Accession |
P05019 |
Purity |
> 95% |
Endotoxin Level |
< 0.1 ng per μg of protein |
Biological Activity |
The ED50 for this effect in a cell proliferation assay using FDC-P1 cells is typically 0.5-1.5
μg/mL. |
Expression System |
E. coli |
Fusion Tag |
No tag |
Predicted Molecular Mass |
2.3 kDa |
Formulation |
Lyophilized from a 0.2 μm filtered solution in Acetonitrile and TFA |
Reconstitution |
Reconstitute in water to a concentration of 0.1-1.0 mg/mL |
Storage & Stability |
Store lyophilized product at -20°C. Once reconstituted, store at -20°C or below. This product is
stable for one year as supplied in lyophilized form. |
FAQ
What is IGF-I (30-41), also known as IGF-I C-Peptide, and how does it differ from other IGF
peptides?
IGF-I (30-41), commonly referred to as the IGF-I C-Peptide, is a fragment of
insulin-like growth factor 1 (IGF-I), which is a hormone with a similar molecular structure to insulin.
Unlike the full-length IGF-I, which contains 70 amino acids, the IGF-I C-Peptide is a specific
12-amino-acid region that plays a distinctive role in the biological activity of the IGFs. The IGF-I
C-Peptide is located on the carboxy-terminal end of the IGF-I molecule. This specific region has been
shown to have unique biological activity, which is separate from the rest of the IGF-I molecule.
While the full IGF-I is known for its involvement in cell growth, development, and survival,
particularly during childhood and adolescence, the C-Peptide may have more specialized functions.
Research has suggested that the IGF-I C-Peptide could be involved in cell signaling pathways that differ
from those activated by the entire IGF-I molecule. This can include more targeted interactions with
specific receptors or downstream molecules, leading to unique cellular responses.
One major area
of interest is how the IGF-I C-Peptide influences cellular proliferation and differentiation,
potentially playing roles in tissue repair and regeneration. Scientists are investigating whether this
C-Peptide has the ability to modulate responses to injury or stress in a manner that might be less
pronounced or altogether absent in the full-length IGF-I. Additionally, while IGF-1 is known for its
implication in glucose regulation and metabolic effects similar to insulin, the C-Peptide’s specific
roles in metabolism are still being elucidated.
Understanding the unique properties of IGF-I
(30-41) helps researchers explore potential therapeutic applications that could harness its specialized
functions. This can include treatments that aim to stimulate tissue repair or mitigate age-related
degeneration without some of the broader effects typical of IGF-I. The precise mechanisms of action for
the IGF-I C-Peptide and its potential applications remain active areas of scientific investigation, with
research aiming to clarify how best to leverage its unique properties for health benefits while
distinguishing them from broader IGF-I effects.
What are the potential benefits of IGF-I
C-Peptide in clinical or therapeutic settings?
The potential benefits of IGF-I C-Peptide in
clinical or therapeutic settings are currently being explored, particularly due to its promising roles
in cellular growth and repair mechanisms. One of the primary areas of interest is its ability to promote
tissue regeneration and repair, which has made it a candidate for therapeutic applications in conditions
related to muscle wasting or injury. The peptide may stimulate the activation of regulatory pathways
that promote the regeneration of muscle tissue, making it particularly relevant in the context of muscle
degeneration diseases, like muscular dystrophy, or age-related muscle loss, known as
sarcopenia.
Moreover, the IGF-I C-Peptide's potential anti-inflammatory properties could make it
beneficial for conditions characterized by chronic inflammation. Inflammation often mediates a range of
degenerative processes, and the modulation of inflammatory responses by IGF-I C-Peptide could provide
therapeutic benefits. This could be particularly advantageous in treating conditions like arthritis,
where reduced inflammation can lead to decreased pain and improved joint function.
Additionally,
there is interest in the neuroprotective effects of IGF-I and its derivatives, including the C-Peptide.
Neurodegenerative diseases, such as Alzheimer's and Parkinson's, might benefit from treatments that can
support neuronal survival and function, and peptides like IGF-I C-Peptide may contribute to these
effects. By promoting neuronal growth and reducing the extent of neural damage, IGF-I C-Peptide could
potentially aid in slowing the progression of such disorders.
Furthermore, the IGF-I C-Peptide
may hold benefits for metabolic disorders, considering the known role of IGF-I in glucose regulation.
While more comprehensive research is needed, early studies suggest that components of the IGF-I
molecule, including the C-Peptide, have the potential to influence glucose uptake and insulin
sensitivity, which could provide a therapeutic angle for managing conditions like
diabetes.
However, it's important to note that while these potential benefits are promising, much
of the current understanding of IGF-I C-Peptide's therapeutic effects is derived from preclinical
studies. Clinical trials will be essential to thoroughly evaluate its efficacy and safety in human
populations, leading to better-informed applications in medicine. As research progresses, scientists are
optimistic about uncovering more specific therapeutic roles and protocols that harness the benefits of
IGF-I C-Peptide.
How does IGF-I C-Peptide interact with cellular mechanisms compared to
full-length IGF-I?
The interaction of IGF-I C-Peptide with cellular mechanisms exhibits notable
differences when compared to the full-length IGF-I. The full-length IGF-I molecule primarily functions
by binding to the IGF-I receptor on the cell surface, initiating a cascade of intracellular signaling
pathways that promote cell proliferation, growth, and differentiation. This signaling is complex,
involving multiple pathways such as the PI3K-Akt pathway, which is critical for cell survival and
metabolism, and the MAPK pathway, which is involved in cell growth and differentiation.
In
contrast, the IGF-I C-Peptide, being a smaller fragment of the molecule, is believed to interact with
cells in a more targeted manner. Although research is ongoing to fully understand its precise pathways,
evidence suggests that the C-Peptide may engage with distinct receptors or modulate the activity of the
same receptors in different ways. This leads to the activation of specific signaling pathways that can
differ from those activated by the full IGF-I molecule.
An important aspect of IGF-I C-Peptide
activity is its potential influence on cellular environments and niche-specific signals. It may serve to
fine-tune cellular responses to growth factors, enhancing specific pathways that contribute to the
structural integrity and function of tissues under stress or repair. This can involve influencing the
local production of cytokines or growth factors that modulate cellular behaviors within a
tissue-specific context.
Furthermore, IGF-I C-Peptide might also exert its effects indirectly by
altering the cellular microenvironment. For instance, it could modify extracellular matrix remodeling,
influencing how cells interact with their surroundings and affecting processes like cell migration,
adhesion, and ultimately tissue formation and repair. This capacity to affect microenvironmental
conditions can play a critical role in regeneration and cellular recovery, setting it apart from the
broader actions of full-length IGF-I.
The specificity of IGF-I C-Peptide's interactions provides
a compelling area of study, especially in contexts where precise signaling without overlapping
widespread metabolic effects of full IGF-I is desired. Researchers continue to investigate these
interactions to better harness their potential in clinical applications, aiming to develop targeted
therapies that leverage the unique capabilities of IGF-I C-Peptide, particularly in the realm of
regenerative medicine and tissue-specific therapies.
What ongoing research is being conducted to
understand and harness the properties of IGF-I C-Peptide?
The ongoing research on IGF-I C-Peptide
spans several exciting areas, primarily focusing on unlocking its potential as a therapeutic agent and
enhancing our understanding of its biological functions. One prominent area of study is the peptide's
role in muscle regeneration and repair. Researchers are investigating how IGF-I C-Peptide can be
utilized to treat muscle-wasting diseases by promoting muscle fiber repair and growth. Animal models are
often used to evaluate the efficacy of IGF-I C-Peptide in preventing muscle atrophy and promoting
recovery following injury. These studies aim to determine optimal dosages and delivery methods that
maximize therapeutic benefits while minimizing any adverse effects.
Additionally, there's a
considerable interest in exploring the neuroprotective roles of IGF-I C-Peptide. Researchers are
conducting preclinical trials examining its effects on neurodegenerative diseases such as Alzheimer's
and Parkinson's. These studies are focused on understanding how IGF-I C-Peptide affects neuronal cell
survival, synaptic function, and overall cognitive health, with some early research indicating it may
help in reducing oxidative stress and inflammation in neural tissues.
Another vital research
front lies in understanding the metabolic effects of IGF-I C-Peptide. Scientists are investigating how
it influences glucose metabolism, insulin sensitivity, and fat metabolism. This line of research is
particularly relevant in the context of obesity and diabetes, where IGF-I C-Peptide may offer a route to
enhance insulin action and achieve better glucose regulation without the pronounced systemic effects of
full-length IGF-I. Such studies aim to highlight pathways that can be modulated to promote better
metabolic health outcomes.
In terms of cancer research, the potential role of IGF-I C-Peptide in
influencing tumor growth and progression is being examined. Since IGF-I is known for its
growth-promoting effects, researchers are carefully studying whether the C-Peptide possesses any
pro-tumorigenic activities or if it might help control tumor growth under certain conditions, such as by
modulating the cellular environment or immune response.
Researchers are also employing advanced
molecular biology techniques to delve deeper into the peptide's interaction with cellular receptors and
intracellular signaling pathways. Investigations with high-throughput screening, proteomics, and
genomics are uncovering possible target molecules and networks influenced by IGF-I C-Peptide, which
could lead to the identification of novel therapeutic targets.
In summary, research on IGF-I
C-Peptide is an active and growing field, with scientists striving to unravel its full potential across
various medical disciplines. The insights gained from ongoing studies promise to enhance our
understanding of how IGF-I C-Peptide can be utilized in innovative therapeutic strategies, potentially
offering new hope for conditions where existing treatments are limited or inadequate.
Can IGF-I
C-Peptide be used safely in humans, and what are the potential risks or side effects?
The safety
and potential risks of using IGF-I C-Peptide in humans are areas of active research, as the peptide's
application moves from preclinical studies to potential clinical trials. As with any bioactive compound,
especially those involved in cell growth and proliferation, understanding the safety profile of IGF-I
C-Peptide is critical to its therapeutic application.
In preclinical models, IGF-I C-Peptide has
shown promise in promoting tissue repair and regeneration with minimal adverse effects reported in these
early stages of research. However, translating these findings to human use requires caution and rigorous
evaluation. The initial safety evaluations in humans would likely involve carefully designed clinical
trials focusing on dosage, delivery methods, and monitoring of adverse effects, closely following
regulatory standards for safety assessments.
One potential area of concern with IGF-I C-Peptide
is its role in cell proliferation. While beneficial in terms of promoting tissue repair, there's always
a risk that stimulating cell growth could potentially encourage the growth of cancerous cells. This is a
common concern with any growth factor-related treatment, and research is needed to delineate the
conditions under which IGF-I C-Peptide might have tumor-promoting effects. Studies would focus on
understanding whether the C-Peptide can discriminate between healthy and tumor tissues, ensuring that
therapies minimize cancer risks.
Side effects of IGF-I and related peptides can include
hypoglycemia, given the insulin-like properties that may affect glucose homeostasis. Therefore, one area
of focus in safety studies would be the peptide’s impact on metabolic parameters, especially in
individuals with pre-existing metabolic disorders like diabetes. Monitoring how it influences insulin
and glucose levels is crucial for assessing any risks of hypoglycemia or other metabolic
disturbances.
Moreover, the immunogenicity of IGF-I C-Peptide is another factor to consider.
Peptides can occasionally trigger immune responses, leading to allergies or other immune-related side
effects. Researchers aim to assess whether IGF-I C-Peptide might induce such responses and how they
could be mitigated, such as through modifications in peptide formulation or delivery
systems.
Ultimately, while the potential therapeutic benefits of IGF-I C-Peptide are promising,
its safety profile in humans needs comprehensive investigation. Well-structured clinical trials with
thorough risk assessment will help in understanding the full scope of potential side effects and
establishing guidelines that maximize treatment efficacy while ensuring patient safety. As the research
progresses, it will offer clearer insights into how IGF-I C-Peptide can be safely integrated into
therapeutic practices, providing new avenues for effective treatments with a secure risk-benefit ratio.