Taiy Chemical
(Ala31,Aib32)-Neuropeptide Y (porcine), (Ala31,A
Synonym (Ala31,Aib32)-NPY (porcine)
Species Porcine
Protein Accession P01303
Purity Greater than 95% as determined by SDS-PAGE
Endotoxin Level < 1 EU/ug
Biological Activity The ED50 as determined by a GTPγS binding assay using rat cerebellar membranes is less than 1.5 nM
Expression System E. coli
Fusion Tag His tag
Predicted Molecular Mass Approximately 5.3 kDa
Formulation Lyophilized from a 0.2 μm filtered solution in Acetonitrile and TFA
Reconstitution It is recommended to reconstitute the lyophilized (Ala31,Aib32)-Neuropeptide Y in sterile 18MΩ-cm H2O not less than 100μg/ml, which can then be further diluted to other aqueous solutions
Storage & Stability Store at -20°C upon receipt. Upon reconstitution store at -20°C or -80°C. Avoid repeated freeze-thaw cycles.
FAQ
What is (Ala31,Aib32)-Neuropeptide Y (porcine) and how is it different from regular Neuropeptide Y?

(Ala31,Aib32)-Neuropeptide Y (porcine) is a synthetic variant of the natural Neuropeptide Y (NPY), specifically designed to include modifications at the 31st and 32nd amino acid positions where alanine (Ala) and aminoisobutyric acid (Aib) replace the usual residues. This engineered peptide is based on the porcine form of NPY, which shares high similarity with human NPY, making it a valuable research tool. The substitutions are strategically placed to alter the biochemical properties of the peptide in a way that helps researchers to better understand the role of these positions in receptor interaction, stability, and functional activity. Regular Neuropeptide Y is a naturally occurring 36-amino acid peptide that plays a significant role in various physiological processes such as energy balance, memory retention, circadian rhythms, and stress responses.

In terms of differences, the modifications in (Ala31,Aib32)-NPY are designed to enhance specific functions or provide stability against enzymatic degradation, which is a common challenge in peptide therapeutics and research. The presence of Aib, a non-canonical amino acid, creates a steric hindrance that limits the conformational flexibility of the peptide backbone, often resulting in increased resistance to proteolytic enzymes. This means that the modified peptide can persist longer in physiological environments, allowing for prolonged activity which is beneficial for research involving extended observation periods. Additionally, these changes may also affect the peptide's binding affinity and selectivity for specific NPY receptor subtypes (Y1, Y2, Y4, and Y5), potentially resulting in altered biological effects compared to the native peptide. Understanding these differences is crucial for researchers who are studying the specific pathways mediated by NPY and the potential therapeutic implications of modulating these pathways. Therefore, the synthetic variant serves as a powerful tool in the detailed dissection of NPY's role in biological systems and the development of related pharmacological agents.

How does (Ala31,Aib32)-Neuropeptide Y (porcine) contribute to research in neurobiology?

(Ala31,Aib32)-Neuropeptide Y (porcine) is a significant asset in neurobiology research, providing insights into the molecular mechanisms of physiological processes such as energy homeostasis, appetite regulation, anxiety, and stress responses. This modified peptide allows researchers to dissect the specific contributions of NPY to these complex biological systems, enabling a more refined understanding of how NPY and its receptor interactions can be manipulated for therapeutic benefit. Due to its structural modifications, (Ala31,Aib32)-NPY offers enhanced stability and selectivity when studied in vitro and in vivo, providing reliable data over extended periods of experimental timeframes. This enhanced stability is particularly advantageous in neurobiology research as it ensures that the peptide’s activity is preserved, thus delivering more consistent and reproducible results compared to its non-modified counterpart.

In neurobiology, understanding the functional role of neuropeptides like NPY is crucial for delineating the signaling pathways and neural circuits that regulate behavior and physiological states. (Ala31,Aib32)-NPY’s ability to bind selectively and with high affinity to specific NPY receptor subtypes enables researchers to map out receptor-specific pathways and their implications in various neurophysiological processes. For example, in appetite and energy homeostasis, altered signaling via NPY receptors is implicated in obesity and metabolic syndrome. By using this synthetic variant, scientists can parse out the contributions of individual receptor subtypes, contributing to the identification of novel targets for therapeutic intervention in metabolic diseases.

Furthermore, in the context of stress and anxiety, (Ala31,Aib32)-NPY offers the ability to explore the role of NPY receptors in stress-induced behaviors more accurately. It allows researchers to assess the potential anxiolytic properties of targeting specific neurons, leading to possible breakthroughs in the treatment of anxiety disorders and related conditions. In summary, (Ala31,Aib32)-Neuropeptide Y (porcine) facilitates a nuanced exploration of neurobiological processes by enabling targeted investigations of NPY pathways, which is essential for developing advanced treatments for a range of neurological and psychological disorders.

Why is the porcine version of this peptide specifically used in research?

The use of the porcine version of (Ala31,Aib32)-Neuropeptide Y in research is largely due to the high degree of homology between porcine and human NPY, which makes it an excellent model for human physiology. Porcine NPY has been extensively studied and characterized, providing a well-understood basis for generating modified peptides like (Ala31,Aib32)-NPY. This variant allows researchers to conduct experiments that are highly relevant to human health, without venturing into human-specific studies initially, offering a balance between relevance and ethical research practices.

Moreover, pigs are considered a valuable animal model in biomedical research because they exhibit many physiological and anatomical similarities to humans, particularly in metabolism, cardiovascular function, and gastrointestinal physiology. By using (Ala31,Aib32)-NPY derived from porcine sources, researchers can tap into this similarity to study the complex interactions within these systems with greater translational potential than might be possible with other animal models. The porcine NPY also presents pragmatic benefits; pigs are a common livestock animal, making it relatively cost-effective and readily available for research purposes.

Porcine models also provide important insights into metabolic and neurological research, areas where NPY plays a critical regulatory role. Studies using porcine NPY can be extrapolated to human health issues such as obesity, diabetes, and mental health disorders, potentially leading to the development of effective therapeutic strategies. By employing a porcine-derived (Ala31,Aib32)-NPY, researchers can assess receptor-ligand interactions, peptide stability, and subsequent biological effects in a way that closely mimics human biological responses. When coupled with other experimental techniques such as imaging and electrophysiology, this peptide makes the porcine system an invaluable resource for preclinical research.

Furthermore, ethical considerations often necessitate the use of non-human models before embarking on human trials. The porcine model permits researchers to perform necessary validation studies and optimize experimental designs in a way that is both ethical and efficient. This approach enables a richer understanding of peptide function and mechanism, ultimately bridging the gap between basic research and clinical application.

How does (Ala31,Aib32)-Neuropeptide Y impact appetite and energy regulation research?

(Ala31,Aib32)-Neuropeptide Y is a critical tool in appetite and energy regulation research, providing valuable insights into the NPY system, which is one of the most potent appetite-stimulating systems in the body. Researchers use this peptide to interrogate the regulatory mechanisms underlying food intake and energy homeostasis, which are fundamentally important to understanding obesity, metabolic syndrome, and related disorders. The structural modifications in (Ala31,Aib32)-NPY are pivotal to these research efforts as they enable prolonged stability and receptor-specific interactions.

NPY is known to exert a strong influence on energy balance by acting in the hypothalamus, a region of the brain that regulates hunger and energy expenditure. It activates NPY receptors such as Y1 and Y5, both of which are involved in stimulating appetite and promoting fat storage. (Ala31,Aib32)-NPY helps researchers tailor experiments to discern the roles of these specific receptors more accurately, leading to the identification of potential intervention points for therapeutics aimed at curbing excessive food intake or altering energy expenditure patterns.

Additionally, the modified peptide aids in understanding the complex feedback loops between peripheral signals (like insulin and leptin) and central metabolic regulators, like NPY. Since peptide stability can often be a limiting factor in such studies due to rapid degradation by enzymes, (Ala31,Aib32)-NPY provides a more reliable tool for long-term experiments. The insights gained can then direct the development of novel drugs aimed at these receptors, potentially resulting in more effective treatments for obesity and metabolic disorders with fewer side effects.

Moreover, (Ala31,Aib32)-NPY allows researchers to create more refined animal models of obesity and metabolic dysfunction by providing a stable, reliable means to modulate the NPY system. These models can show how chronic NPY activation affects diet-induced obesity or how altering this signaling pathway might influence weight loss strategies or exercise efficiency. In summary, the role of (Ala31,Aib32)-Neuropeptide Y in appetite and energy regulation research is invaluable, as it provides the necessary biochemical tools to delve deeper into the mechanisms that control energy balance, ultimately aiming to translate these findings into therapeutic innovations.

Can (Ala31,Aib32)-Neuropeptide Y (porcine) be used to understand stress and anxiety disorders?

Absolutely, (Ala31,Aib32)-Neuropeptide Y plays a significant role in advancing our understanding of stress and anxiety disorders. The NPY system is intricately involved in modulating stress and anxiety responses, with various studies indicating that NPY has anxiolytic-like effects, which can buffer against the stress-induced activation of the hypothalamic-pituitary-adrenal (HPA) axis. This peptide variant allows researchers to obtain clearer insights into the biochemical and physiological pathways that govern these complex emotional states.

(Ala31,Aib32)-NPY's resistance to degradation and enhanced receptor selectivity make it an ideal candidate for detailed temporal studies exploring the dynamics of NPY signaling during stress responses. Researchers can utilize this peptide to clarify how NPY signaling via specific receptors such as Y1 and Y2 influences emotional and behavioral outcomes under stress. For instance, through animal models of stress-induced anxiety, it is possible to observe changes in the activity of brain regions involved in emotional regulation, such as the amygdala and prefrontal cortex, following administration of this peptide.

In particular, this modified peptide helps dissect the interaction between NPY and other neurotransmitter systems, such as the GABAergic and glutamatergic systems, which are also implicated in anxiety and stress responses. The findings from such studies have the potential to inform the development of new therapeutic targets for anxiety disorders. Additionally, (Ala31,Aib32)-NPY can be used in translational research, aiming to bridge findings from animal models to potential human applications. Exploring how this peptide modulates stress-related pathways might highlight innovative approaches to treat psychiatric conditions associated with dysregulated stress responses, including post-traumatic stress disorder (PTSD) and generalized anxiety disorder (GAD).

Furthermore, the pharmacokinetic advantages of (Ala31,Aib32)-NPY over native NPY permit chronic administration studies, which are essential for understanding changes over prolonged stress exposure periods. This can be pivotal in research aiming to understand the long-term impacts of chronic stress and identify intervention points that may alleviate these effects. In conclusion, (Ala31,Aib32)-Neuropeptide Y (porcine) is a robust research tool that advances our understanding of the mechanisms behind stress and anxiety disorders and aids in the development of novel therapeutic strategies.
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