* Please kindly note that our products and services can only be used to support research purposes (Not for clinical use).
Creative Peptides is committed to making contributions to biopharmaceutical research, specializing in providing amino acid products. Our products are designed to meet the different needs of the global audience, and at the same time achieve unparalleled outstanding achievements in the biomedical field.
Amino acids are the building blocks of proteins, which are essential macromolecules for life. They play crucial roles in various biological processes, including the formation of structural components, enzyme function, and signaling within cells.
Amino acid structure: Amino acids are organic compounds characterized by having both an amino group (-NH2) and a carboxyl group (-COOH) attached to a central carbon atom, known as the alpha carbon. Additionally, they have a variable side chain, denoted as R group, which determines the specific properties of each amino acid.
Properties: Amino acids can be acidic, basic, polar, or nonpolar, depending on the nature of their side chains. This diversity in side chain chemistry contributes to the diversity of protein structures and functions.
Essential amino acids: These are amino acids that cannot be synthesized by the body and must be obtained from the diet. There are nine essential amino acids for humans: histidine, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tryptophan, and valine.
Non-essential amino acids: These are amino acids that the body can synthesize on its own, thus not required to be consumed through the diet. Examples include alanine, asparagine, aspartic acid, and glutamic acid.
Conditional amino acids: These are amino acids that are usually non-essential but may become essential under certain conditions, such as illness or stress, where the body's demand for them exceeds its ability to produce them. Examples include arginine, cysteine, glutamine, tyrosine, glycine, ornithine, proline, and serine.
There are only 20 amino acids in the genetic code, and the 20 animo acids can be classified in many ways. They can be classified according to polarity (polar amino acids and no polar amino acids), pH level, and the type of side chain group, such as aliphatic, aromatic, containing hydroxyl or sulfur, etc. The amino acids reference charts are as follows.
20 amino acids structures and names.pdf
Amino Acids with Hydrophobic Side Chain – Aliphatic
Amino Acids with Hydrophobic Side Chain – Aromatic
Amino Acids with Polar Neutral Side Chains
Amino Acids with Electricaly Charged Side Chains – Acidic
Amino Acids with Electricaly Charged Side Chains – Basic
Unique Amino Acids
Properties of Common Amino Acids
Amino Acids with Hydrophobic Side Chain - Aliphatic
Alanine, Ala, A | Valine, Val, V | Leucine, Leu, L | Isoleucine, Ile, I |
Amino Acids with Hydrophobic Side Chain – Aromatic
Tryptophan, Trp, W | Tyrosine, Tyr, Y | Phenylalanine, Phe, F |
Amino Acids with Polar Neutral Side Chains
Asparagine, Asn, N | Cysteine, Cys, C | Glutamine, Gln, Q |
Methionine, Met, M | Serine, Ser, S | Threonine, Thr, T |
Amino Acids with Electricaly Charged Side Chains – Acidic
Aspartic acid, Asp, D | Glutamic acid, Glu, E |
Amino Acids with Electricaly Charged Side Chains – Basic
Arginine, Arg, R | Histidine, His, H | Lysine, Lys, K |
Unique Amino Acids
Glycine, Gly, G | Proline, Pro, P |
Properties of Common Amino Acids
3-Letter Symbol | 1-Letter Symbol | Name | Side Chains | Molecular Formula | CAS.No | Molecular weight | PI | PKa | PKb | R Group |
---|---|---|---|---|---|---|---|---|---|---|
Gly | G | Glycine | Hydrophilic | C2H5NO2 | 56-40-6 | 75.07 | 6.06 | 2.4 | 9.8 | -H |
Ala | A | Alanine | Hydrophobic | C3H7NO2 | 56-41-7 | 89.09 | 6.11 | 2.4 | 9.9 | -CH₃ |
Val | V | Valine | Hydrophobic | C5H11NO2 | 72-18-4 | 117.2 | 6 | 2.4 | 9.7 | -CH-(CH3)2 |
Leu | L | Leucine | Hydrophobic | C6H13NO2 | 61-90-5 | 131.2 | 6.01 | 2.3 | 9.7 | -CH2-CH(CH3)2 |
Ile | I | Isoleucine | Hydrophobic | C6H13NO2 | 73-32-5 | 131.2 | 6.05 | 2.3 | 9.8 | -CH(CI3)-CI2-CI3 |
Phe | F | Phenylalanine | Hydrophobic | C9H11NO2 | 63-91-2 | 165.2 | 5.49 | 2.2 | 9.3 | -CH2-C6H5 |
Trp | W | Tryptophane | Hydrophobic | C11H12N2O2 | 73-22-3 | 204.2 | 5.89 | 2.5 | 9.4 | -C8NH6 |
Tyr | Y | Tyrosine | Hydrophobic | C9H11NO3 | 60-18-4 | 181.2 | 5.64 | 2.2 | 9.2 | -CH2-C6H4-OH |
Asp | D | Asparagine | Acidic | C4H7NO4 | 6899-03-2 | 133.1 | 2.85 | 2 | 9.9 | -CI2-COOH |
Asn | N | Aspartic acid | Hydrophilic | C4H8N2O3 | 70-47-3 | 132.1 | 5.41 | 2.1 | 8.7 | -CI2-CONH2 |
Glu | E | Glutamic acid | Acidic | C5H9NO4 | 56-86-0 | 147.1 | 3.15 | 2.1 | 9.5 | -(CH2)2-COOH |
Lys | K | Lysine | Basic | C6H14N2O2 | 56-87-1 | 146.2 | 9.6 | 2.2 | 9.1 | -(CH2)4-NH2 |
Gln | Q | Glutamine | Hydrophilic | C5H10N2O3 | 56-85-9 | 146.2 | 5.65 | 2.2 | 9.1 | -(CH2)2-CONH2 |
Met | M | Methionine | Hydrophobic | C5H11NO2S | 63-68-3 | 149.2 | 5.74 | 2.1 | 9.3 | -(CI2)-S-CI3 |
Ser | S | Serine | Hydrophilic | C3H7NO3 | 56-45-1 | 105.1 | 5.68 | 2.2 | 9.2 | -CI2-OH |
Thr | T | Threonine | Hydrophilic | C4H9NO3 | 72-19-5 | 119.1 | 5.6 | 2.1 | 9.1 | -CH(CI3)-OH |
Cys | C | Cysteine | Hydrophilic | C3H7NO2S | 52-90-4 | 121.2 | 5.05 | 1.9 | 11 | -CI2-SH |
Pro | P | Proline | Hydrophobic | C5H9NO2 | 147-85-3 | 115.1 | 6.3 | 2 | 11 | -C3H6 |
His | H | Hlstidine | Basic | C6H9N3O2 | 71-00-1 | 155.2 | 7.6 | 1.8 | 9.3 | |
Arg | R | Argnine | Basic | C6H14N4O2 | 74-79-3 | 174.2 | 10.8 | 1.8 | 9 |
PI is the pH of the isoelectric point
PKa is the negative of the logarithm of the dissociation constant for the -COOH group
PKb is the negative of the logarithm of the dissociation constant for the –NH3+ group
Protein synthesis: Amino acids are the building blocks of proteins. During protein synthesis, amino acids are linked together through peptide bonds to form polypeptide chains, which then fold into specific three-dimensional structures to perform various functions in the body.
Enzyme function: Many enzymes, which are biological catalysts that facilitate biochemical reactions in the body, are proteins composed of amino acids. The specific sequence and arrangement of amino acids in enzymes determine their catalytic activity and substrate specificity, allowing them to accelerate chemical reactions necessary for metabolism, digestion, and other physiological processes.
Neurotransmitter synthesis: Amino acids serve as precursors for the synthesis of neurotransmitters, which are chemical messengers involved in transmitting signals between neurons (nerve cells) in the nervous system. For example, the neurotransmitters serotonin, dopamine, and gamma-aminobutyric acid (GABA) are synthesized from specific amino acids (tryptophan, tyrosine/phenylalanine, and glutamate, respectively).
Hormone regulation: Some amino acids are involved in the synthesis of hormones, which are signaling molecules that regulate various physiological processes in the body. For instance, thyroid hormones (thyroxine and triiodothyronine) contain the amino acid tyrosine, while insulin, a hormone that regulates blood sugar levels, consists of two polypeptide chains linked by disulfide bonds, which are formed between cysteine residues.
Pharmaceuticals: Amino acids serve as the foundation for synthesizing pharmaceuticals. They are used in the production of antibiotics, vaccines, and various medications. For example, antibiotics like penicillin are produced from amino acids.
Medical applications: Amino acids have medical applications beyond pharmaceuticals. They are used in intravenous (IV) solutions for patients who cannot consume nutrients orally. Amino acids are also used in wound healing and tissue repair.
Food industry: Amino acids are used as flavor enhancers and additives in the food industry. Monosodium glutamate (MSG), derived from glutamic acid, is a common flavor enhancer. Amino acids also play a role in fermentation processes, such as in brewing and winemaking.
Cosmetics and personal care products: Amino acids are used in cosmetics and personal care products for their moisturizing and conditioning properties. They can help improve skin texture, promote hair health, and enhance the effectiveness of skincare products.
Agriculture: Amino acids are used in agriculture as fertilizers to improve soil quality and promote plant growth. They are also used in animal feed to enhance growth and productivity in livestock.
Biotechnology and research: Amino acids are essential in biotechnology for protein engineering and the production of recombinant proteins. They are also used as markers in biochemical research and as standards in analytical chemistry techniques like chromatography.
Textile industry: Amino acids are utilized in the production of synthetic fibers like nylon. These fibers are used in textiles, carpets, and industrial applications due to their strength and durability.
Biodegradable polymers: Amino acids are used in the production of biodegradable polymers, which have applications in packaging materials, biomedical implants, and environmentally friendly plastics.
Amino acids are essential nutrients for cell cultures. Most animal cells in culture require a source of amino acids, which are the building blocks of proteins in cells. Most commonly used media for mammalian cell culture contains all 20 standard amino acids, including essential amino acids that cannot be synthesized by cells and must be provided in the medium. Amino acid composition and concentration in the medium can influence cell growth and productivity. Therefore, the optimization of amino acid concentrations in the culture medium is an important aspect of cell culture process development.
Supplementing cell culture media with specific amino acids can improve cell growth and protein production. For example, glutamine is a commonly supplemented amino acid due to its role in protein synthesis and energy production. However, glutamine can rapidly degrade in culture medium, leading to the release of toxic ammonia. To overcome this challenge, a more stable form of glutamine, alanyl-glutamine, is commonly used in cell culture.
Unnatural amino acids are synthetic or modified amino acids that are not naturally found in proteins. They are often used in peptide synthesis to introduce specific properties or functionalities into peptides, which can be useful in various research and medical applications. Here are some common types and uses of unnatural amino acids in peptide synthesis:
Fluorescent amino acids: These amino acids contain fluorescent groups that emit light upon excitation. They are widely used in studying protein-protein interactions, protein localization, and dynamics.
Photoactivatable amino acids: These amino acids contain groups that can be activated by light to undergo chemical reactions. They are used in studying protein function, protein-protein interactions, and mapping protein-protein interfaces.
Crosslinking amino acids: Amino acids with reactive groups that can form covalent bonds with nearby amino acids are used for crosslinking peptides or proteins. This helps in studying protein structure, protein-protein interactions, and stabilizing protein complexes.
Bioorthogonal amino acids: These amino acids have functional groups that react selectively with each other in the presence of other biomolecules. They are useful for labeling proteins in complex biological environments.
Chemical modification amino acids: Amino acids with specific chemical functionalities can be incorporated into peptides to introduce post-translational modifications or to facilitate conjugation with other molecules.
Structurally modified amino acids: Amino acids with modified side chains or backbone structures can be used to stabilize peptide conformations, enhance protease resistance, or modulate peptide-receptor interactions.
Diverse functional groups: Unnatural amino acids can be designed with a wide range of functional groups such as azides, alkynes, ketones, and aldehydes, which can be used for various bioconjugation strategies.
Optically active amino acids: Amino acids with chiral centers can be synthesized in optically pure forms, enabling the synthesis of peptides with defined stereochemistry for studying structure-activity relationships.
By incorporating these unnatural amino acids into peptides, researchers can tailor the properties and functions of peptides for specific applications in drug discovery, diagnostics, materials science, and chemical biology.
1. What types of amino acid products do you offer?
We offer a comprehensive range of amino acid products, including individual amino acids, amino acid mixes, custom formulations, and specialty amino acids tailored to specific research needs.
2. Are your amino acid products suitable for cell culture?
Yes, our amino acid products are specifically designed for cell culture applications. They are highly purified and free from contaminants, making them ideal for supporting cell growth and proliferation.
3. Do you provide certificates of analysis (COA) for your products?
Absolutely. We provide detailed certificates of analysis with each batch of our amino acid products, documenting their purity, composition, and quality control testing results.
4. What is the shelf life of your amino acid products?
Our amino acid products are manufactured under strict quality control conditions to ensure maximum stability and shelf life. Typically, our products have a shelf life of at least two years when stored according to the provided instructions.
5. Can you provide custom formulations of amino acids?
Yes, we offer custom formulation services to meet your specific research requirements. Whether you need a unique amino acid mix or a specialized formulation, our team of experts can work with you to develop a product tailored to your needs.
6. Are your amino acid products suitable for in vivo studies?
While our amino acid products are primarily designed for in vitro applications such as cell culture, we can provide specially formulated products for in vivo studies upon request. Please contact us to discuss your specific needs.
7. What quality control measures do you have in place for your amino acid products?
We adhere to stringent quality control measures throughout the manufacturing process to ensure the purity, consistency, and integrity of our amino acid products. This includes rigorous testing for contaminants, verification of composition, and adherence to industry standards.
Reference
Creative Peptides has accumulated a huge library of peptide knowledge including frontier peptide articles, application of peptides, useful tools, and more!
GRK2i, a GRK2 inhibitory polypeptide, specifically inhibits Gβγ activation of GRK2. It corresponds to the Gβγ-bi ...
Antazoline is a drug used in the treatment of atrial fibrillation (AF), and its formula is C17H19N3. In fact, th ...
DAMME (DA) is a guanine, often referred to as FK 33-824 (FK), which is a long-acting enkephalin analog. Natur ...
Trifluoroacetyl tripeptide-2 (TFA-T2) is an innovative peptide compound that has garnered significant attention in dermatolog ...
Muramyl dipeptide (MDP) is the smallest structural unit with immune activity in the skeleton of bacille calmette ...