Synonym |
β-Endorphin (28-31) (human) |
Species |
Human |
Protein Accession |
P01189 |
Purity |
> 95% |
Endotoxin Level |
< 1.0 EU per 1 μg of protein |
Biological Activity |
Not available |
Expression System |
Chemical synthesis |
Fusion Tag |
None |
Predicted Molecular Mass |
427.5 Da |
Formulation |
Lyophilized from a 0.2 μm filtered solution in Acetonitrile and TFA |
Reconstitution |
Centrifuge vial before opening. Reconstitute in sterile PBS, pH 7.4 to a concentration of 100
μg/mL. |
Storage & Stability |
Store lyophilized protein at -20°C. Aliquot reconstituted protein and store at -20°C. Avoid
repeated freeze-thaw cycles. |
FAQ
What is β-Endorphin (28-31) (human), and what is its significance in scientific
research?
β-Endorphin (28-31) (human) is a peptide fragment derived from the β-endorphin protein,
consisting of four amino acids (Tyr-Gly-Gly-Phe). As a part of the larger β-endorphin structure, it
holds immense importance as it mimics some of the biological activities of the full protein.
β-Endorphin, in general, is an endogenous opioid neuropeptide and peptide hormone, and it is one of the
several endorphins known for their ability to modulate the body's reaction to pain and stress.
Researchers are particularly interested in β-Endorphin (28-31) due to its potential analgesic properties
and its role in various physiological processes.
Research into β-Endorphin (28-31) largely aims
at understanding the mechanisms of pain relief and stress reduction without the side effects typically
associated with synthetic opioids. Unlike full-length β-endorphin, this specific fragment provides
insights into the part of the peptide that may be responsible for certain selective interactions or
biological responses. Because β-Endorphin (28-31) is a central component in pain modulation pathways, it
has been the focus of studies exploring non-addictive pain management options, which is critically
important given the current global challenges related to opioid addiction.
Additionally,
β-Endorphin (28-31) is involved in studies related to its effects on the immune system, mood
stabilization, and overall homeostasis. Due to its shorter structure, it may play a role in modulating
immune responses without fully engaging the opioid receptors, an aspect highly valued in
immunologically-centered research. Scientists are continuously exploring whether this peptide can elicit
specific responses that are therapeutically beneficial without unwarranted side effects. This makes
β-Endorphin (28-31) a crucial molecule for advancing our understanding of non-opioid dependant receptor
pathways and offers promising avenues for therapeutic applications with reduced adverse
effects.
How does β-Endorphin (28-31) contribute to the understanding of pain
modulation?
β-Endorphin (28-31) plays a critical role in advancing our understanding of pain
modulation by acting as a representative model to study the specific interactions and pathways involved
in the body's natural response to painful stimuli. This peptide fragment is integrated into broader
research examining how endorphins—natural substances in the body—mediate the sensation of pain.
β-Endorphin itself is a significant neuromodulator and analgesic agent, while its fragment, β-Endorphin
(28-31), is used to narrow down the effects that specific sequences within the molecule have on pain
perception.
Research indicates that β-Endorphin (28-31) binds selectively to certain opioid
receptors in the brain, predominantly the mu-opioid receptors, which are crucial for pain management. By
studying this interaction, researchers can isolate the effects of binding to this subset of receptors
and potentially identify pathways that could be harnessed for innovative pain relief therapies. Due to
its selective nature, β-Endorphin (28-31) can help uncover subtle differences in receptor activity that
are not apparent when studying the larger, more complex β-Endorphin molecule.
Additionally,
understanding the way β-Endorphin (28-31) modulates pain provides insights into developing more precise
therapeutic agents that harness natural endorphin-like effects while minimizing known side effects such
as dependency or tolerance associated with conventional opioid medications. This specificity is key in
distinguishing the effects of natural pain suppression pathways and synthetically engineered
alternatives. By harnessing the body's own pain regulation mechanisms through fragments like β-Endorphin
(28-31), researchers are paving the way for novel pain management techniques that could revolutionize
clinical pain therapies.
Moreover, this understanding has a broader implication in the
development of drugs targeting other types of pain modalities, which include neuropathic and
inflammatory pain, further enhancing the scope of therapeutic intervention. Besides, due to the lesser
side effects and potential non-addictive properties outlined by studies into β-Endorphin (28-31), it has
encouraged interest in how endogenous peptides can interact selectively with receptors to treat pain
conditions more effectively and safely.
What potential therapeutic applications are being
explored with β-Endorphin (28-31)?
Researchers are exploring a range of potential therapeutic
applications for β-Endorphin (28-31) due to its selective interactions and operability without the
extensive side effects associated with full-length β-endorphins or synthetic opioids. One of the
prominent areas of interest is pain management. As β-Endorphin (28-31) may modulate pain by engaging
with specific opioid receptors, there is significant potential to develop new pain relief therapies that
do not carry the risk of dependency. In chronic pain management, the peptide could offer a more
sustainable alternative with reduced risks, enhancing the quality of life for patients dealing with
long-term pain conditions.
Beyond pain relief, this peptide fragment is studied for its potential
anti-inflammatory properties. Researchers are examining how β-Endorphin (28-31) influences various
biochemical pathways linked to inflammation, with the prospect of developing new anti-inflammatory
treatments. This research has implications for managing chronic inflammatory diseases, such as arthritis
and inflammatory bowel disease, where current treatments can cause adverse side effects or are
inadequate.
Furthermore, studies also indicate that β-Endorphin (28-31) might hold potential in
the field of mental health. The role of endorphins, including fragments like β-Endorphin (28-31), in
mood regulation suggests that they could be beneficial in treating mood disorders like depression or
anxiety. By harnessing the body’s natural mechanisms for mood enhancement, it could contribute to
developing treatments that provide efficacy similar to current antidepressants but with fewer side
effects and long-lasting benefits.
In addition, β-Endorphin (28-31) is being explored in immune
modulation. As this peptide could potentially fine-tune immune responses without fully activating opioid
pathways, this aspect is particularly enticing for researchers interested in autoimmunity and
hypersensitivity conditions. By moderating exaggerated immune responses, β-Endorphin (28-31) could
contribute to therapies that prevent tissue damage in autoimmune diseases.
Lastly, β-Endorphin
(28-31) is also part of studies concerning opioid addiction treatments. Since it interacts with opioid
receptors in a more controlled manner, understanding these interactions might aid in developing
medications or therapies that alleviate withdrawal symptoms or decrease reliance on synthetic opioids in
those with addiction, ultimately offering a holistic strategy to combat the opioid crisis plaguing many
communities.
What challenges do researchers face while studying β-Endorphin (28-31), and how are
they addressing these challenges?
Studying β-Endorphin (28-31) involves a set of unique
challenges that researchers are striving to address through various innovative methods. One of the
primary challenges is the short biological half-life of peptide fragments like β-Endorphin (28-31).
Peptides are quickly degraded by proteases in the body, making it difficult to sustain their activity
long enough to investigate their full therapeutic potential or realize their applications effectively.
Researchers are addressing this limitation by exploring various peptide stabilization techniques, such
as chemical modifications or encapsulation strategies that can enhance the stability and bioavailability
of these peptides in physiological conditions.
Another significant challenge is the specificity
of action required when dealing with opioid-related peptides. β-Endorphin (28-31) needs to demonstrate
its potential without triggering the adverse effects associated with other opioid peptides, such as
dependency, tolerance, and respiratory depression. Researchers are employing advanced receptor-binding
studies and sophisticated molecular modeling approaches to ensure that the desired selective activity is
achieved. By pinpointing the optimal receptor interactions at a molecular level, scientists can better
design analogs or delivery methods that preserve the therapeutic benefits while minimizing side
effects.
Researchers also face hurdles in large-scale synthesis and production of β-Endorphin
(28-31). Producing peptides in sufficiently high quantities and purities for research can be costly and
technically demanding. To tackle this, research institutions are adopting recombinant DNA technology and
advanced peptide synthesis techniques to enhance yield and lower production costs. These innovations
allow for extensive preclinical testing and refine peptides for human trials.
An additional layer
of complexity arises from variability in response among different biological systems, which can make
interpretation of experimental data challenging. To manage this, comprehensive in vitro and in vivo
assays are conducted across diverse models to obtain a holistic view of biological activity and
therapeutic efficacy. Multi-disciplinary collaborations involving biologists, chemists, pharmacologists,
and clinicians are instrumental in navigating these challenges and pushing the boundaries of current
research.
Moreover, ethical issues concerning the testing of opioid-like peptides in human
subjects, given the potential for misuse, require careful attention. Adhering to strict ethical
guidelines and ensuring transparency in clinical trial designs help in addressing these issues. Through
these efforts, researchers are steadily advancing the understanding of β-Endorphin (28-31) and its
potential as a safe and effective therapeutic option.
What future advancements and areas of
exploration hold potential for β-Endorphin (28-31)?
Looking forward, β-Endorphin (28-31) presents
an exciting frontier for advancements and exploration in multiple fields of biomedical research. One
compelling direction is the continued quest for non-addictive analgesics. The focus here is on further
deepening the understanding of how β-Endorphin (28-31) can mediate pain relief without engaging the full
spectrum of opioid receptor activity that leads to dependency. Emerging technologies such as
cryo-electron microscopy and nuclear magnetic resonance are enhancing our ability to visualize receptor
binding at an atomic level, which could significantly aid in designing drugs tailored to exploit
beneficial interactions while avoiding deleterious effects.
Another promising area is
personalized medicine, where β-Endorphin (28-31) could be harnessed in developing bespoke treatment
regimens. By examining variations in individual opioid receptor configurations and responses, it might
be possible to tailor therapies based on personal genetic makeup, thereby optimizing efficacy and
minimizing side effects. With the advent of pharmacogenomics, researchers are hopeful that such precise
and customized therapeutic interventions could become a reality.
In addition, β-Endorphin
(28-31)’s role in immune modulation is a growing area of interest. Exploration into how this peptide
influences immune responses could contribute to groundbreaking treatment approaches for autoimmune
diseases or conditions where immune dampening is advantageous. Researchers are particularly keen on
exploring this in conjunction with immunotherapy, thus expanding the arsenal of strategies available to
treat complex conditions such as cancer or chronic inflammatory disorders.
Neuroscience research
also stands to gain from progress with β-Endorphin (28-31), particularly in understanding the intricate
dynamics of pain-mood pathways and how these might be manipulated to alleviate conditions like
depression or anxiety. Continued research in this area holds promise for developing more effective
mental health therapies that utilize the body’s innate biochemical pathways for mood
stabilization.
Furthermore, innovative drug delivery systems are being developed to improve the
efficiency with which β-Endorphin (28-31) reaches its targets. Techniques such as nanoparticle carriers
or smart hydrogels are being investigated for their ability to facilitate controlled release of the
peptide, enhancing its therapeutic window. This could also apply in acute settings, where rapid pain or
stress relief is necessary, providing quicker onset of action while retaining prolonged therapeutic
effects.
Overall, with multi-disciplinary research synergizing insights from chemistry,
biomedicine, and pharmacology, new light is being cast on β-Endorphin (28-31) and its diverse
applications. As research evolves, the likelihood of integrating β-Endorphin (28-31) into daily medical
practice grows, heralding a new chapter in treating pain, inflammation, and mood disorders with
precision and compassion.