VIP

Vasoactive Intestinal Peptide
Shipped with Ice Packs
In Stock

Description

Introduction to Vasoactive Intestinal Peptide (VIP)

Vasoactive Intestinal Peptide (VIP) is a 28-amino acid neuropeptide belonging to the glucagon/secretin superfamily, functioning as a ligand for class II G protein–coupled receptors . It is widely expressed in vertebrates, including the gastrointestinal tract, central nervous system, and endocrine organs, with roles in vasodilation, immune modulation, and metabolic regulation . VIP has a short plasma half-life (~2 minutes) , limiting its therapeutic applications unless stabilized via chemical modifications .

Molecular Structure and Chemical Properties

Key structural and biochemical characteristics of VIP:

PropertyValueSource
Molecular FormulaC₁₄₇H₂₃₇N₄₃O₄₃S
Molecular Weight3326.8 g/mol
CAS Registry Number37221-79-7
Amino Acid SequenceHSDAVFTDNYTRLRKQMAVKKYLNSILN
Receptor TargetsVPAC1, VPAC2

VIP’s structure includes a highly basic N-terminal domain critical for receptor binding . Its instability in biological systems has driven research into PEGylation and stapled peptide analogs to enhance pharmacokinetics .

Anti-Inflammatory and Immunomodulatory Effects

VIP downregulates proinflammatory cytokines (TNF-α, IL-6, IL-12) and upregulates anti-inflammatory IL-10 . Clinical studies highlight its efficacy in:

  • Chronic Inflammatory Response Syndrome (CIRS): VIP nasal spray reverses grey matter atrophy and improves neurocognitive outcomes .

  • Autoimmune Diseases: Reduces inflammation in murine arthritis and asthma models .

  • Ocular Infections: Enhances growth factors (EGF, FGF, HGF) and angiogenic molecules (VEGF-A) to promote corneal repair .

Metabolic Regulation

VIP enhances insulin sensitivity and glucose metabolism, offering adjunct benefits for patients on GLP-1 receptor agonist therapy . Preclinical data suggest VIP modulates glycogenolysis and lipid metabolism .

Clinical Applications vs. Research Advancements

CategoryClinical ApplicationsEmerging Research
InflammationCIRS management, sarcoidosis VIP-PEG conjugates for enhanced stability
NeurologyNeuroprotection in Alzheimer’s models VIP receptor antagonists (ANT308) for T-cell activation
OncologyPro-angiogenic roles in breast/prostate cancer
Regulatory StatusFDA reviewing removal from compounding list SNV (VIP analog) for osteolysis prevention

Challenges and Future Directions

  • Pharmacokinetic Limitations: VIP’s rapid degradation necessitates drug delivery innovations (e.g., nasal sprays, PEGylation) .

  • Regulatory Hurdles: The FDA’s 2019 proposal to exclude VIP from compounding lists risks limiting access for CIRS patients .

  • Dual Roles in Disease: While VIP suppresses inflammation, it may promote tumor angiogenesis, requiring targeted receptor modulation .

Product Specs

Description
Vasoactive Intestinal Peptide Synthetic is a single, non-glycosylated polypeptide chain containing 28 amino acids with a molecular mass of 3325 Daltons and a molecular formula of C147H238N44O42S.
Physical Appearance
Sterile Filtered White lyophilized (freeze-dried) powder.
Formulation
The protein was lyophilized with no additives.
Solubility
Reconstitute the lyophilized Vasoactive Intestinal Peptide in sterile 18MΩ-cm H2O at a concentration not less than 100 µg/ml. This solution can be further diluted to other aqueous solutions.
Stability
Lyophilized Vasoactive Intestinal Peptide is stable at room temperature for 3 weeks but should be stored desiccated below -18°C. Upon reconstitution, Vasoactive Intestinal Peptide should be stored at 4°C for 2-7 days. For future use, store below -18°C. For long term storage, add a carrier protein (0.1% HSA or BSA). Avoid freeze-thaw cycles.
Purity
Greater than 97.0% as determined by RP-HPLC analysis.
Amino Acid Sequence

H-His-Ser-Asp-Ala-Val-Phe-Thr-Asp-Asn-Tyr-Thr-Arg-Leu-Arg-Lys-Gln-Met-Ala-Val-Lys-Lys-Tyr-Leu-Asn-Ser-Ile-Leu-Asn-NH2.

Q&A

The following FAQs address common inquiries in academic research contexts related to Vertically Integrated Projects (VIP), synthesized from multidisciplinary research principles and program implementation data. Questions are stratified by complexity and supported with methodological frameworks from peer-reviewed studies and program analyses.

Advanced Research Questions

What optimization methods address multidisciplinary communication barriers?

From 869 student cohort analysis :

Barrier TypeMitigation StrategySuccess Rate
Technical LexiconWeekly cross-domain glossary sessions82% improvement
Methodology GapsPaired programming (CS+ME teams)73% efficacy
Temporal AlignmentAgile sprints synchronized across majors68% adherence

How to design statistically robust VIP assessment frameworks?

Four-pillar assessment model derived from :

  • Signal Detection Theory: EEG data validation protocols

  • Longitudinal Analysis: 3-year persistence tracking matrices

  • Multivariate Regression: Policy impact coefficients (β=0.68 for design sequence credits)

  • Ethnographic Validation: 360° peer evaluations across disciplines

Technical Implementation

How to quantify knowledge transfer in VIP hierarchies?

Modified PageRank algorithm applied to mentorship networks:

TRscore=1Ni=1N(0.85CdirectTmeetings+0.15PindirectDproximity)TR_{score} = \frac{1}{N}\sum_{i=1}^{N}\left(0.85\frac{C_{direct}}{T_{meetings}} + 0.15\frac{P_{indirect}}{D_{proximity}}\right)

Where CdirectC_{direct} = documented code reviews, PindirectP_{indirect} = publication co-authorship links

Product Science Overview

Discovery and Structure

VIP was first discovered in the 1970s. It is synthesized as a precursor molecule of 170 amino acids, which includes a signal peptide of 22 amino acids. This precursor is then cleaved to produce the active peptide of 28 amino acids . The gene encoding VIP is located on chromosome 6 in humans .

Expression and Distribution

VIP is produced in various tissues of vertebrates, including the gut, pancreas, cortex, and suprachiasmatic nuclei of the hypothalamus in the brain . It is highly conserved across species, with identical sequences found in humans, cows, pigs, rats, dogs, and goats .

Functions

VIP has a wide range of physiological functions:

  • Cardiovascular System: It stimulates contractility in the heart and causes vasodilation, which helps lower arterial blood pressure .
  • Digestive System: VIP increases glycogenolysis and relaxes the smooth muscle of the trachea, stomach, and gallbladder . It also stimulates the secretion of electrolytes and water by the intestinal mucosa .
  • Nervous System: VIP functions as a neuromodulator and neurotransmitter. It regulates smooth muscle activity, epithelial cell secretion, and blood flow in the gastrointestinal tract .
Receptors and Signal Transduction

The VIP receptor is a member of a unique class of G protein-coupled receptors. These receptors share significant sequence homology, distinguishing them from the rhodopsin/beta-adrenergic family (class I) . VIP shares 68% sequence homology with pituitary adenylyl cyclase-activating peptide (PACAP) .

Clinical Significance

VIP has been studied for its potential therapeutic applications due to its vasodilatory and anti-inflammatory properties. It is also involved in the regulation of immune responses and has been implicated in various diseases, including asthma, chronic obstructive pulmonary disease (COPD), and inflammatory bowel disease (IBD) .

Quick Inquiry

Personal Email Detected
Please use an institutional or corporate email address for inquiries. Personal email accounts ( such as Gmail, Yahoo, and Outlook) are not accepted. *
© Copyright 2024 Thebiotek. All Rights Reserved.