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Elucidating how bamboo salt interacts with supported lipid membranes: influence of alkalinity on membrane fluidity

Authors
Jeong, Jong HeeChoi, Jae-HyeokKim, Min ChulPark, Jae HyeonHerrin, Jason ScottKim, Seung HyunLee, HaiwonCho, Nam-Joon
Issue Date
Jul-2015
Publisher
Springer Verlag
Keywords
Cell membrane; Lipid bilayer; Mobility; Monovalent cation; Fluorescence recovery after photobleaching
Citation
European Biophysics Journal, v.44, no.5, pp 383 - 391
Pages
9
Indexed
SCI
SCIE
SCOPUS
Journal Title
European Biophysics Journal
Volume
44
Number
5
Start Page
383
End Page
391
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/156848
DOI
10.1007/s00249-015-1043-8
ISSN
0175-7571
1432-1017
Abstract
Bamboo salt is a traditional medicine produced from sea salt. It is widely used in Oriental medicine and is an alkalizing agent with reported antiinflammatory, antimicrobial and chemotherapeutic properties. Notwithstanding, linking specific molecular mechanisms with these properties has been challenging to establish in biological systems. In part, this issue may be related to bamboo salt eliciting nonspecific effects on components found within these systems. Herein, we investigated the effects of bamboo salt solution on supported lipid bilayers as a model system to characterize the interaction between lipid membranes and bamboo salt. The atomic composition of unprocessed and processed bamboo salts was first analyzed by mass spectrometry, and we identified several elements that have not been previously reported in other bamboo salt preparations. The alkalinity of hydrated samples was also measured and determined to be between pH 10 and 11 for bamboo salts. The effect of processed bamboo salt solutions on the fluidic properties of a supported lipid bilayer on glass was next investigated by fluorescence recovery after photobleaching (FRAP) analysis. It was demonstrated that, with increasing ionic strength of the bamboo salt solution, the fluidity of a lipid bilayer increased. On the contrary, increasing the ionic strength of near-neutral buffer solutions with sodium chloride salt diminished fluidity. To reconcile these two observations, we identified that solution alkalinity is critical for the effects of bamboo salt on membrane fluidity, as confirmed using three additional commercial bamboo salt preparations. Extended-DLVO model calculations support that the effects of bamboo salt on lipid membranes are due to the alkalinity imparting a stronger hydration force. Collectively, the results of this work demonstrate that processing of bamboo salt strongly affects its atomic composition and that the alkalinity of bamboo salt solutions contributes to its effect on membrane fluidity.
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