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磷脂单分子层下草酸钙一水合物晶体的定向生长。

Oriented growth of calcium oxalate monohydrate crystals beneath phospholipid monolayers.

作者信息

Letellier S R, Lochhead M J, Campbell A A, Vogel V

机构信息

Department of Bioengineering, University of Washington, Seattle, USA.

出版信息

Biochim Biophys Acta. 1998 Mar 12;1380(1):31-45. doi: 10.1016/s0304-4165(97)00121-9.

Abstract

Oriented calcium oxalate crystals have been grown beneath phospholipid monolayers at the air-solution interface from supersaturated calcium oxalate solutions. Mature calcium oxalate crystals grown beneath zwitterionic dipalmitoylphosphatidylcholine (DPPC) monolayers exhibit the characteristic morphology of calcium oxalate monohydrate (COM) crystals with the elongated (101) crystal face preferentially oriented parallel to the plane of the monolayer. Calcium oxalate crystals grown beneath negatively-charged dimyristoylphosphatidylserine (DMPS) monolayers also show a preferential orientation with respect to the monolayer; they do not, however, exhibit the characteristic COM morphology. Raman spectroscopy strongly suggests that the crystals grown beneath either DPPC or DMPS monolayers are the monohydrate phase of calcium oxalate; therefore, differences in crystal morphology are not due to differences in the crystalline phase. Dimyristoylphosphatidylethanolamine (DMPE), dimyristoylphosphatidic acid (DMPA), eicosanoic acid (C20), and eicosanol (C20-OH) monolayers have also been studied to help elucidate the mechanisms of interaction between the lipid monolayers and the calcium oxalate crystals. We discuss the roles of lattice matching, hydrogen bonding, stereochemistry and electrostatics on crystal orientation and morphology.

摘要

在空气 - 溶液界面的磷脂单分子层下方,已从过饱和草酸钙溶液中生长出取向的草酸钙晶体。在两性离子二棕榈酰磷脂酰胆碱(DPPC)单分子层下方生长的成熟草酸钙晶体呈现出一水合草酸钙(COM)晶体的特征形态,其拉长的(101)晶面优先平行于单分子层平面取向。在带负电荷的二肉豆蔻酰磷脂酰丝氨酸(DMPS)单分子层下方生长的草酸钙晶体相对于单分子层也显示出优先取向;然而,它们并未呈现出特征性的COM形态。拉曼光谱强烈表明,在DPPC或DMPS单分子层下方生长的晶体是草酸钙的一水合物相;因此,晶体形态的差异并非由于晶相的不同。还研究了二肉豆蔻酰磷脂酰乙醇胺(DMPE)、二肉豆蔻酰磷脂酸(DMPA)、二十烷酸(C20)和二十烷醇(C20 - OH)单分子层,以帮助阐明脂质单分子层与草酸钙晶体之间的相互作用机制。我们讨论了晶格匹配、氢键、立体化学和静电作用在晶体取向和形态方面的作用。

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