When exploring the world of biochemistry and molecular research, the VIP peptide sequence often emerges as a primary point of interest. As someone who has spent considerable time analyzing the structural characteristics of various molecules, I have found the Vasoactive Intestinal Polypeptide (VIP) to be one of the most fascinating subjects due to its highly conserved nature across different species.
The Structural Foundation
At its core, VIP is a peptide of 28 amino acid residues. This specific arrangement is what defines its functional identity. When we look at the H-His-Ser-Asp-Ala-Val-Phe-Thr-Asp-Asn-Tyr-Thr-Arg-Leu-Arg sequence—often represented in its full 28-amino acid form—we are looking at a molecule that is remarkably stable.
From my personal review of laboratory data, it is impor Vasoactive intestinal peptide gene polymorphisms tant to note that VIP is a neuropeptide that belongs to the glucagon/secretin superfamily. This classification is vital for those interested in the ligand-receptor dynamics of class II G protein-coupled receptors. A key detail often discussed in research circles is that VIP has 67% sequence homology with PACAP-27, and it shares roughly 68 percent sequence homology with pituitary adenylyl cyclase-activating polypeptides. This structural similarity is why researchers often study them in tandem.
Key Characteristics and Observations
In Vasoactive intestinal peptide | C147H237N43O43S - PubChem my experience analyzing molecular data, the following details are essential for anyone attempting to understand this polypeptide:
* Origin: VIP was first isolated and sequenced from pig small intestine, which paved the way for modern mapping of the DNA sequences coding for the VIP and its precursor molecules.
* Conservation: The amino acid order is identical in humans, bovine, porcine, and rat models. This evolutionary conservation underscores its fundamental role in biological systems.
* Synthesis: VIP is synthesized from a peptide precursor molecule known as prepro-VIP, which also contains a related peptide called PHM (peptide with N-terminal histidine).
* Biological Context: VIP is a neuropeptide involved in a dive DNA sequences coding for the VIPand PHM-27 hormones are located in two different exons. Southern blot analysis with genomic DNA suggested that a single copy of Read more rse array of physiological processes, primarily by activating Apr 6, 2011—Vasoactive intestinalpeptide(VIP) is a 28-amino acid neuropeptide which belongs to a glucagon/secretin superfamily, the ligand of class II G protein-coupled Read more the PACAP subfamily of class B1 G protein-coupled receptors. It enables hormone activity and acts as a neuromodulator within various tissues.
Practical Considerations for Researchers
When sourcing or reviewing data on VIP (Vasoactive Intestinal Peptide), researchers often encounter specific identifiers. For instance, the neuroblastoma VIP-cDNA sequence is a common reference point for those examining gene expression. Furthermore, the sequence is often cited in studies regarding its interaction with VPAC1 and VPAC2 receptors.
If you are by IV Seoane·2018·Cited by 24—TheVIPgene wassequencedin patients with extremely high/lowVIPlevels, measured by enzyme immunoassay. Sixteen single nucleotide Read more Molecular Weight. 3326.8 g/mol. Computed by PubChem 2.2 (PubChem release 2025.04.14) ; IUPAC Condensed.H-His-Ser-Asp-Ala-Val-Phe-Thr-Asp-Asn-Tyr-Thr-Arg-Leu-ArgRead more looking to order materials for analytical purposes, you will frequently see the shorthand His-Ser-Asp-Ala used to denote the N-terminal start of the chain. Always ensure that the purity and the analytical verification (such as mass spectrometry confirming the 3323.77 Da molecular weight) align with your specific project requirements.
Final Thoughts
The study of the VIP peptide sequence is an excellent entry point into understanding how specific amino acid arrangements dictate function. Whether you are Structure and expression of the gene encoding investigating the Vasoactive intestinal polypeptide (VIP) for its role in cellular signaling or its structural relationship to other neuropeptides, the precision of its 28-residue chain remains a cornerstone of molecular biology.
As I continue to track the latest developments in this field, the consistency of the VIP structure continues to provide a reliable baseline for further inquiry. Always rely on peer-reviewed documentation and standardized chemical databases to verify the identity and properties of the peptide you are working with.