Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters










Database
Language
Publication year range
2.
Cell Mol Life Sci ; 59(12): 2210-5, 2002 Dec.
Article in English | MEDLINE | ID: mdl-12568347

ABSTRACT

Polar plants and animals survive in subzero waters (-2 degrees C) and many of these marine organisms produce antifreeze proteins (AFPs) to better adapt themselves to these conditions. AFPs prevent the growth of ice crystals which disrupt cellular membranes and destroy cells by inhibiting crystallization of water within the organism. The hydrophilic extract of an Antarctic sponge Homaxinella balfourensis exhibited a non-colligative freezing point depression effect on the crystal morphology of water. The extract was purified by repeated reverse phase high-pressure liquid chromatography, then assayed and shown to contain several AFPs. The major peptide was isolated, analyzed using matrix-assisted laser desorption ionization mass spectrometry and the partial structure of the peptide identified through amino acid sequencing. AFPs have potential applications in agriculture, medicine and the food industry.


Subject(s)
Antifreeze Proteins/isolation & purification , Porifera/chemistry , Animals , Antarctic Regions , Antifreeze Proteins/chemistry , Antifreeze Proteins/metabolism , Cold Temperature , Crystallization , Porifera/metabolism , Sequence Analysis, Protein
3.
Biomacromolecules ; 1(2): 268-74, 2000.
Article in English | MEDLINE | ID: mdl-11710110

ABSTRACT

Recently antifreeze proteins (AFP) have been the subject of many structure-function relationship studies regarding their antifreeze activity. Attempts have been made to elucidate the structure-function relationship by various amino acid substitutions, but to our knowledge there has been no successful from first principles design of a polypeptide that would bind to designated ice planes along a specific direction. In this paper we show the results of our first attempt on an entirely de novo design of an alanine-lysine-rich antifreeze polypeptide. This 43 residue alanine-lysine peptide exhibits characteristic nonequilibrium freezing point depression and binds to the designated (210) planes of ice along the [122] vector. The structural and thermodynamic properties of this polypeptide were determined using circular dichroism spectroscopy and its nonequilibrium antifreeze properties were investigated using an ice-etching method and nanoliter osmometry.


Subject(s)
Alanine/chemistry , Lysine/chemistry , Peptides/chemistry , Amino Acid Sequence , Chemical Phenomena , Chemistry, Physical , Circular Dichroism , Crystallization , Freeze Etching , Freezing , Molecular Conformation , Molecular Sequence Data , Structure-Activity Relationship , Thermodynamics , Water/chemistry
SELECTION OF CITATIONS
SEARCH DETAIL
...