Synonym |
Thrombin receptor-activating peptide 6 amide |
Species |
Human |
Protein Accession |
P55085 |
Purity |
Greater than 95% as determined by HPLC and SDS-PAGE |
Endotoxin Level |
Less than 1 EU/ug |
Biological Activity |
The ED50 for this effect is typically 40-150 nM |
Expression System |
E. coli |
Fusion Tag |
His-tag |
Predicted Molecular Mass |
1082.2 Da |
Formulation |
Lyophilized from a 0.2 μm filtered solution in Acetonitrile and TFA |
Reconstitution |
Centrifuge the vial prior to opening. Reconstitute in water to a concentration of 0.1-1.0 mg/ml.
|
Storage & Stability |
Store at -20°C. Stable for 12 months from the date of receipt when stored at -20°C. |
FAQ
What is TRAP-6 amide and how does it work in the body?
TRAP-6 amide is a synthetic peptide that
is often referenced in scientific research and medical studies. Its primary function is to mimic
thrombin receptor activating peptides, which play a crucial role in the body’s coagulation system. One
of the most fascinating aspects of TRAP-6 amide is its ability to activate the protease-activated
receptors (PARs), particularly PAR-1, which are found in many tissues and have various roles in cellular
signaling. Activation of these receptors can lead to a cascade of intracellular events, impacting things
like inflammation, vascular tone, and even cell proliferation. This makes TRAP-6 amide a potent tool in
experimental setups designed to explore cardiovascular and clotting processes, allowing researchers to
derive insights into how blood vessels respond to different stimuli or how platelets aggregate. In
medical research, understanding how TRAP-6 amide influences these pathways can potentially open the door
for new treatments related to clotting disorders or cardiovascular diseases, where the fine-tuning of
PAR signaling might mitigate pathological clot formation or excessive bleeding. Moreover, TRAP-6 amide
has become valuable in cancer research, as PAR-1 is often overexpressed in various tumor types,
influencing metastatic potential and tumor growth. By studying TRAP-6 amide’s interaction with these
receptors, researchers aim to develop targeted therapies that may interfere with cancer progression by
blocking aberrant signaling pathways. Thus, while TRAP-6 amide itself may not be a therapeutic agent,
the insights gained from its study have far-reaching implications, making it a cornerstone in the
toolkit of researchers keen on advancing our understanding of complex biological systems. Its role in
various experimental applications underscores its versatility and importance in the landscape of
biomedical research.
What are the potential applications of TRAP-6 amide in medical
research?
TRAP-6 amide serves as a critical tool in biological and medical research due to its
ability to mimic natural thrombin receptor activating peptides. This peptide's functionality opens the
door to numerous applications, particularly because of its involvement in activating protease-activated
receptors (PARs). One significant application has been in the field of cardiovascular research. By
enabling controlled activation of PAR-1, TRAP-6 amide helps researchers explore the complexities of
platelet aggregation and the mechanisms behind thrombus formation. Understanding these processes is
vital for developing new treatments and drugs aimed at preventing pathological clotting disorders, such
as deep vein thrombosis or myocardial infarctions, which continue to be leading causes of morbidity and
mortality worldwide. In cancer research, TRAP-6 amide has offered substantial insights into cancer
metastasis. Since PAR-1 is frequently overexpressed in malignant tissues, researchers utilize TRAP-6
amide to help delineate the role of this receptor in tumor growth and the metastatic spread of cancer
cells. More specifically, it assists in understanding how interrupting PAR signaling can slow the spread
of cancer, thereby leading to new therapeutic avenues targeting these pathways. Additionally, TRAP-6
amide is being explored in neurological studies as protease-activated receptors, which are critical to
neuron signaling, maintain homeostasis and mediate responses to injuries or diseases in the nervous
system. With neurodegenerative diseases being a rising concern globally, research into PAR modulators
that include TRAP-6 amide could pave the way for developing neuromodulatory agents capable of
alleviating symptoms or slowing the progression of these disorders. Furthermore, inflammation research
benefits significantly from TRAP-6 amide, as PARs play a key role in inflammation and immunity. Through
investigating TRAP-6 amide's action on these receptors, there is potential to discover novel
anti-inflammatory drugs that better address chronic inflammatory conditions, providing relief to
millions suffering worldwide. Each of these applications exemplifies the broad utility and potential
impact of TRAP-6 amide in advancing medical therapies and improving patient outcomes.
How is
TRAP-6 amide used in laboratory settings, and what precautions should researchers take?
TRAP-6
amide serves widely in laboratory settings due to its utility in mimicking thrombin receptor activation,
primarily engaging the PAR-1 receptor, and enabling researchers to simulate and study complex biological
pathways and processes. This versatility makes it a staple in cardiovascular, cancer, and neurological
research, where controlled receptor activation is necessary for examining physiological and
pathophysiological states. In cardiovascular studies, researchers apply TRAP-6 amide to observe platelet
aggregation and vascular response dynamics, critical for understanding and preventing thrombotic
diseases. Utilizing assays and in vitro models, they can delineate the implications of thrombin-like
activity on cellular components, thus facilitating the discovery of antithrombotic therapies. For cancer
research, the peptide provides insights into PAR-mediated cellular processes like proliferation and
migration, shedding light on tumor growth and metastasis mechanisms. In these settings, it is frequently
employed in cell culture experiments where its interaction with overexpressed PAR-1 in cancer cells can
be closely monitored, helping in the development of targeted cancer therapies. Despite its benefits,
handling TRAP-6 amide requires strict adherence to laboratory safety protocols. As a synthetic peptide,
it should be treated with care, utilizing appropriate personal protective equipment (PPE) like gloves
and lab coats to prevent contamination or inadvertent exposure. Researchers must also ensure that TRAP-6
amide is stored under recommended conditions, usually in a desiccated and temperature-controlled
environment, to preserve its stability and activity. Procedures involving the peptide should be
conducted in well-ventilated or fume-hood-equipped areas to limit inhalation risks or aerosol exposure.
Furthermore, rigorous protocols for waste disposal must be followed to minimize environmental
contamination and potential hazards resulting from synthetic peptides. By maintaining these precautions
while using TRAP-6 amide, researchers effectively leverage its potentials in a controlled, safe manner,
contributing to advancements in various biomedical fields.
Are there any known side effects or
risks associated with TRAP-6 amide in research applications?
When utilized in research settings,
TRAP-6 amide is primarily employed as a tool for understanding biological and cellular processes rather
than being directly applied in therapeutic scenarios involving human or animal subjects. However, like
any biologically active compound, careful considerations are necessary as there can be implicit risks or
nuances to be aware of, to ensure experimental integrity and safety. Experimental use of TRAP-6 amide
can inherently come with potential cellular responses that must be thoroughly understood; if unforeseen
interactions occur, they might skew the accuracy of a study's results. Thus, managing variables such as
concentration, exposure duration, and the biological model used is critical. Overdosage or extended
exposure to TRAP-6 amide in vitro can provoke exaggerated cellular responses that do not naturally
occur, consequently misleading conclusions about physiological processes. Analyzing results adequately
mandates that researchers account for these factors to differentiate between normal and experimental
artifacts. Additionally, technicians and experimenters must meticulously observe protocols to maintain
biological activity and experimental repeatability. The handling specifics mean that contamination or
degradation, perhaps due to improper storage or material handling, could inadvertently affect findings
and necessitate repeat trials, taxing resources and time. Furthermore, chemical mishandlings such as
spills or inappropriate disposal routes pose potential risks to laboratory safety and environmental
well-being, thereby emphasizing robust adherence to waste management protocols as critical for
minimizing downstream effects. As a research tool, while it targets specified receptors, non-target
effects should be monitored. In cellular contexts where receptor expression varies or extra-paracrine
signaling mechanisms are involved, TRAP-6 amide's activity could have off-target effects that must be
distinguished and characterized to harness its full potential responsibly. The success of TRAP-6 amide
in research therefore hinges not only on its biological efficacy but equally on diligent observance of
best laboratory practices and regulatory protocols that protect users and experimental frameworks from
unintended side effects or liabilities.
How does TRAP-6 amide contribute to advancements in
cardiovascular disease research?
TRAP-6 amide plays a pivotal role in cardiovascular disease
research by simulating thrombin receptor activation, specifically interacting with the
protease-activated receptor, PAR-1. This interaction is fundamental in advancing the understanding of
thrombosis and hemostasis — crucial processes that, when dysregulated, are central to the pathology of
cardiovascular diseases. Researchers leverage TRAP-6 amide to induce controlled activation of PAR-1,
enabling the study of platelet aggregation and endothelial cell function in various disease models,
which are essential for elucidating the pathways leading to conditions such as heart attacks, strokes,
and other thrombotic events. The interaction with PAR-1 offers insights into vascular biology,
particularly regarding the regulation of vascular tone and inflammation within the arterial walls. In
pathological contexts such as atherosclerosis, chronic activation of PARs is implicated in plaque
formation and instability, events that can precipitate acute cardiovascular events. Through the targeted
and controlled use of TRAP-6 amide, researchers can dissect the contributions of such receptors to
diseases, experiment with therapeutic interventions that modulate these pathways, or identify novel
markers of disease progression. Furthermore, studying the nuances of thrombin receptor signaling
provides clues to preventing adverse events associated with clot formation, like myocardial infarction
or thrombotic strokes, by developing medications that can selectively inhibit or modulate PAR activity,
reducing the risk of excessive clotting while avoiding undesirable bleeding tendencies seen with some
antithrombotic therapies. TRAP-6 amide, therefore, creates a bridge between basic biological research
and clinical applications, ushering in new paradigms for managing and treating cardiovascular ailments.
By refining our understanding of molecular mechanisms underlying cardiovascular disorders, TRAP-6 amide
positions itself as a vital asset not merely in advancing scientific knowledge but also in translating
these discoveries into real-world clinical solutions, paving the way for innovative therapeutic
strategies that could revolutionize cardiovascular disease management in the future.