2017
Theoretical and experimental study of the antifreeze protein AFP752, trehalose and dimethylsulfoxide cryoprotection mechanism: correlation with cryopreserved cell viability
KRATOCHVÍLOVÁ, I, M GOLAN, K POMEISL, J RICHTER, S SEDLÁKOVÁ et. al.Základní údaje
Originální název
Theoretical and experimental study of the antifreeze protein AFP752, trehalose and dimethylsulfoxide cryoprotection mechanism: correlation with cryopreserved cell viability
Autoři
KRATOCHVÍLOVÁ, I, M GOLAN, K POMEISL, J RICHTER, S SEDLÁKOVÁ, J ŠEBERA, J MIČOVÁ, Martin FALK, I FALKOVÁ, D ŘEHA, K W ELLIOTT, K VARGA, S E FOLLETT a D ŠIMEK
Vydání
RSC Advances, Cambridge, Royal Society of Chemistry, 2017, 2046-2069
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Stát vydavatele
Česká republika
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 2.936
UT WoS
000393741900048
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 19. 12. 2019 13:42, doc. RNDr. Martin Falk, Ph.D.
Anotace
V originále
In this work the physico-chemical properties of selected cryoprotectants (antifreeze protein TrxA-AFP752, trehalose and dimethyl sulfoxide) were correlated with their impact on the constitution of ice and influence on frozen/thawed cell viability. The freezing processes and states of investigated materials solutions were described and explained from a fundamental point of view using ab initio modelling (molecular dynamics, DFT), Raman spectroscopy, differential scanning calorimetry and X-ray diffraction. For the first time, in this work we correlated the microscopic view (modelling) with the description of the frozen solution states and put these results in the context of human skin fibroblast viability after freezing and thawing. DMSO and AFP had different impacts on their solution's freezing process but in both cases the ice crystallinity size was considerably reduced. DMSO and AFP treatment in different ways improved the viability of frozen/thawed cells.
Návaznosti
GA16-12454S, projekt VaV |
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GBP302/12/G157, projekt VaV |
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NV16-29835A, projekt VaV |
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