≥99% PURITY GUARANTEEDTHIRD-PARTY TESTEDSAME-DAY SHIPPING USACOA WITH EVERY ORDERFREE SHIPPING $200+
Back to Peptide Information

Introduction to Peptides

A comprehensive introduction to peptides, their structure, classification, and fundamental concepts in peptide chemistry.

8 min readOctober 15, 2025BioInfinity Lab

Research Use Only: All products on this site are for Research and Development use only. Products are not intended for human consumption. The statements made within this website have not been evaluated by the US Food and Drug Administration.

What is a Peptide?

A peptide is a short chain of amino acid monomers linked together by peptide bonds. These bonds are formed through a condensation reaction between the carboxyl group of one amino acid and the amino group of another. Peptides are distinguished from proteins primarily by their size—peptides typically contain fewer than 50 amino acids, while proteins contain 50 or more.

Peptide Classification by Size

Peptides are classified based on the number of amino acids they contain:

  • Dipeptides: Two amino acids joined by a single peptide bond
  • Tripeptides: Three amino acids linked by two peptide bonds
  • Oligopeptides: Short chains typically containing 2-20 amino acids
  • Polypeptides: Longer chains containing 20-50 amino acids
  • Proteins: Very long chains with more than 50 amino acids

Amino Acids: The Building Blocks

There are 20 standard amino acids that serve as the building blocks for peptides. Each amino acid has a unique side chain (R group) that determines its chemical properties. These amino acids can be categorized as:

  • Nonpolar (Hydrophobic): Glycine, Alanine, Valine, Leucine, Isoleucine, Proline, Phenylalanine, Methionine, Tryptophan
  • Polar Uncharged: Serine, Threonine, Cysteine, Tyrosine, Asparagine, Glutamine
  • Acidic (Negatively Charged): Aspartic acid, Glutamic acid
  • Basic (Positively Charged): Lysine, Arginine, Histidine

Peptide Structure

The structure of peptides is described at multiple levels:

  • Primary Structure: The linear sequence of amino acids
  • Secondary Structure: Local folding patterns like alpha helices and beta sheets
  • Tertiary Structure: The overall three-dimensional shape

Biological Significance

Peptides play crucial roles in numerous biological processes. They function as hormones, neurotransmitters, growth factors, and signaling molecules. Many naturally occurring peptides regulate physiological functions including metabolism, immune response, and cell signaling.

Peptides in Research

Synthetic peptides have become invaluable tools in biomedical research. They are used to study protein-protein interactions, develop diagnostic assays, and investigate cellular mechanisms. The ability to synthesize peptides with specific sequences allows researchers to probe biological systems with precision.

Key Takeaways

  • Peptides are short chains of amino acids linked by peptide bonds
  • They differ from proteins primarily in length (typically <50 amino acids)
  • The 20 standard amino acids provide diverse chemical properties
  • Peptide structure ranges from primary sequence to 3D conformation
  • Synthetic peptides are essential tools in modern research

Explore Our Research Peptides

Premium quality with ≥99% purity. COA included with every order.

Shop Now

Disclaimer: These Peptides are for Research use Only and not intended for Human Use. The information provided in this article is for educational purposes only and should not be construed as medical advice.