TY - JOUR
T1 - Atomic force microscopy imaging of ice crystal surfaces formed in aqueous solutions containing ice-binding proteins
AU - Chasnitsky, Michael
AU - Cohen, Sidney R.
AU - Rudich, Yinon
AU - Braslavsky, Ido
N1 - Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2023/1/1
Y1 - 2023/1/1
N2 - Ice-binding proteins (IBPs) allow organisms to survive below the freezing point by modulating ice crystal growth. These proteins act by binding to ice surfaces, thus inhibiting ice growth. Until now, high-resolution imaging of ice growing in the presence of IBPs has not been possible. We developed a unique in-situ technique that enables atomic force microscopy (AFM) imaging of ice formation and growth in the ice-IBP system. The new technique enables controlling the growth of ice crystals under a strong and focused thermal gradient. We present images of ice crystals with sub-ten nanometer resolution. Ice was grown in the presence of two different IBPs that exhibit specific and unique structures. This development opens the path for fine elucidation of the interaction of IBPs with growing ice surfaces as well as with other frozen systems at unprecedented high resolution. Furthermore, with the exception of crystals growing in thin films, this is the first demonstration for imaging a growing crystal immersed in its own melt with AFM.
AB - Ice-binding proteins (IBPs) allow organisms to survive below the freezing point by modulating ice crystal growth. These proteins act by binding to ice surfaces, thus inhibiting ice growth. Until now, high-resolution imaging of ice growing in the presence of IBPs has not been possible. We developed a unique in-situ technique that enables atomic force microscopy (AFM) imaging of ice formation and growth in the ice-IBP system. The new technique enables controlling the growth of ice crystals under a strong and focused thermal gradient. We present images of ice crystals with sub-ten nanometer resolution. Ice was grown in the presence of two different IBPs that exhibit specific and unique structures. This development opens the path for fine elucidation of the interaction of IBPs with growing ice surfaces as well as with other frozen systems at unprecedented high resolution. Furthermore, with the exception of crystals growing in thin films, this is the first demonstration for imaging a growing crystal immersed in its own melt with AFM.
KW - Antifreeze proteins
KW - Atomic force microscopy
KW - Crystal morphology
KW - Gradient freeze technique
KW - Ice
KW - Ice binding proteins
UR - http://www.scopus.com/inward/record.url?scp=85141503457&partnerID=8YFLogxK
U2 - 10.1016/j.jcrysgro.2022.126961
DO - 10.1016/j.jcrysgro.2022.126961
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AN - SCOPUS:85141503457
SN - 0022-0248
VL - 601
JO - Journal of Crystal Growth
JF - Journal of Crystal Growth
M1 - 126961
ER -