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In chemistry, an amphiphile (from Greek αμφις (amphis) 'both' and φιλíα 'love, friendship'), or amphipath, is a chemical compound possessing both hydrophilic (water-loving, polar) and lipophilic (fat-loving, nonpolar) properties. [1] Such a compound is called amphiphilic or amphipathic. Amphiphilic compounds include surfactants and ...
[3] [4] [5] Amphipols can be used to fold denatured membrane proteins to their native form [6] [7] and have proven particularly precious in the field of single-particle electron cryo-microscopy (cryo-EM; see e.g. [8] [9]).The properties and uses of amphipols and other non-conventional surfactants are the subject of a book by Jean-Luc Popot. [10]
Increasing the amphiphile concentration beyond the point where lamellar phases are formed would lead to the formation of the inverse topology lyotropic phases, namely the inverse cubic phases, the inverse hexagonal columnar phase (columns of water encapsulated by amphiphiles, (H II) and the inverse micellar cubic phase (a bulk liquid crystal ...
IUPAC definition: Micelle: Particle of colloidal dimensions that exists in equilibrium with the molecules or ions in solution from which it is formed. [1] [2] Micelle (polymers) Organized auto-assembly formed in a liquid and composed of amphiphilic macromolecules, in general amphiphilic di- or tri-block copolymers made of solvophilic and ...
Peptide amphiphiles were developed in the 1990s. They were first described by the group of Matthew Tirrell in 1995. [5] [6] These first reported PA molecules were composed of two domains: one of lipophilic character and another of hydrophilic properties, which allowed self-assembly into sphere-like supramolecular structures as a result of the association of the lipophilic domains away from the ...
The characterization of mechanical properties in polymers typically refers to a measure of the strength, elasticity, viscoelasticity, and anisotropy of a polymeric material. The mechanical properties of a polymer are strongly dependent upon the Van der Waals interactions of the polymer chains, and the ability of the chains to elongate and align ...
Because of their amphiphilic structures, the polymers have surfactant properties that make them useful in industrial applications. Among other things, they can be used to increase the water solubility of hydrophobic, oily substances or otherwise increase the miscibility of two substances with different hydrophobicities.
An approximate rule of thumb for hydrophilicity of organic compounds is that solubility of a molecule in water is more than 1 mass % if there is at least one neutral hydrophile group per 5 carbons, or at least one electrically charged hydrophile group per 7 carbons. [4] Hydrophilic substances (ex: salts) can seem to attract water out of the air.