TY - JOUR
T1 - New insights into Ice growth and melting modifications by antifreeze proteins
AU - Bar-Dolev, Maya
AU - Celik, Yeliz
AU - Wettlaufer, J. S.
AU - Davies, Peter L.
AU - Braslavsky, Ido
PY - 2012/12/7
Y1 - 2012/12/7
N2 - Antifreeze proteins (AFPs) evolved in many organisms, allowing them to survive in cold climates by controlling ice crystal growth. The specific interactions of AFPs with ice determine their potential applications in agriculture, food preservation and medicine. AFPs control the shapes of ice crystals in a manner characteristic of the particular AFP type. Moderately active AFPs cause the formation of elongated bipyramidal crystals, often with seemingly defined facets, while hyperactive AFPs produce more varied crystal shapes. These differentmorphologies are generally considered to be growth shapes. In a series of bright light and fluorescent microscopy observations of ice crystals in solutions containing different AFPs, we show that crystal shaping also occurs during melting. In particular, the characteristic ice shapes observed in solutions ofmost hyperactiveAFPs are formed during melting.We relate these findings to the affinities of the hyperactive AFPs for the basal plane of ice. Our results demonstrate the relation between basal plane affinity and hyperactivity and show a clear difference in the ice-shaping mechanisms of most moderate and hyperactive AFPs. This study provides key aspects associated with the identification of hyperactive AFPs.
AB - Antifreeze proteins (AFPs) evolved in many organisms, allowing them to survive in cold climates by controlling ice crystal growth. The specific interactions of AFPs with ice determine their potential applications in agriculture, food preservation and medicine. AFPs control the shapes of ice crystals in a manner characteristic of the particular AFP type. Moderately active AFPs cause the formation of elongated bipyramidal crystals, often with seemingly defined facets, while hyperactive AFPs produce more varied crystal shapes. These differentmorphologies are generally considered to be growth shapes. In a series of bright light and fluorescent microscopy observations of ice crystals in solutions containing different AFPs, we show that crystal shaping also occurs during melting. In particular, the characteristic ice shapes observed in solutions ofmost hyperactiveAFPs are formed during melting.We relate these findings to the affinities of the hyperactive AFPs for the basal plane of ice. Our results demonstrate the relation between basal plane affinity and hyperactivity and show a clear difference in the ice-shaping mechanisms of most moderate and hyperactive AFPs. This study provides key aspects associated with the identification of hyperactive AFPs.
KW - Antifreeze proteins
KW - Crystal growth
KW - Hyperactive antifreeze proteins
KW - Ice-binding proteins
KW - Ice-structuring proteins
KW - Melting shapes
UR - http://www.scopus.com/inward/record.url?scp=84868546369&partnerID=8YFLogxK
U2 - 10.1098/rsif.2012.0388
DO - 10.1098/rsif.2012.0388
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C2 - 22787007
AN - SCOPUS:84868546369
SN - 1742-5689
VL - 9
SP - 3249
EP - 3259
JO - Journal of the Royal Society Interface
JF - Journal of the Royal Society Interface
IS - 77
ER -