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Peptoid drug discovery and optimization via surface X-ray scattering.通过表面 X 射线散射进行肽类药物的发现和优化。
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The L Phase of Pulmonary Surfactant.肺表面活性剂的 L 相。
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Hydrophobic interactions modulate antimicrobial peptoid selectivity towards anionic lipid membranes.疏水性相互作用调节抗菌肽类似物对阴离子脂质膜的选择性。
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Interfacial curvature effects on the monolayer morphology and dynamics of a clinical lung surfactant.界面曲率对临床用肺表面活性剂单层形态和动力学的影响。
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The role of multilayers in preventing the premature buckling of the pulmonary surfactant.多层膜在预防肺表面活性剂过早失稳中的作用。
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Effect of cholesterol on the molecular structure and transitions in a clinical-grade lung surfactant extract.胆固醇对临床级肺表面活性剂提取物分子结构及转变的影响
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Cyclization Improves Membrane Permeation by Antimicrobial Peptoids.环化提高抗菌肽肽的膜通透性。
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Monomolecular Siloxane Film as a Model of Single Site Catalysts.单分子硅氧烷膜作为单活性位催化剂的模型。
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Modification of Salmonella Lipopolysaccharides Prevents the Outer Membrane Penetration of Novobiocin.沙门氏菌脂多糖的修饰可防止新生霉素穿透外膜。
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肺泡表面活性剂囊泡诱导的肺表面活性剂膜的结构变化。

Structural Changes in Films of Pulmonary Surfactant Induced by Surfactant Vesicles.

机构信息

Department of Physics, Center for Molecular Study of Condensed Soft Matter (μCoSM), Pritzker Institute of Biomedical Science and Engineering, Illinois Institute of Technology, Chicago, Illinois 60616, United States.

X-ray Science Division, Argonne National Laboratory, 9700 South Cass Avenue, Lemont, Illinois 60439, United States.

出版信息

Langmuir. 2020 Nov 17;36(45):13439-13447. doi: 10.1021/acs.langmuir.0c01813. Epub 2020 Oct 20.

DOI:10.1021/acs.langmuir.0c01813
PMID:33080138
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8754419/
Abstract

When compressed by the shrinking alveolar surface area during exhalation, films of pulmonary surfactant reduce surface tension to levels at which surfactant monolayers collapse from the surface . Vesicles of pulmonary surfactant added below these monolayers slow collapse. X-ray scattering here determined the structural changes induced by the added vesicles. Grazing incidence X-ray diffraction on monolayers of extracted calf surfactant detected an ordered phase. Mixtures of dipalmitoyl phosphatidylcholine and cholesterol, but not the phospholipid alone, mimic that structure. At concentrations that stabilize the monolayers, vesicles in the subphase had no effect on the unit cell, and X-ray reflection showed that the film remained monomolecular. The added vesicles, however, produced a concentration-dependent increase in the diffracted intensity. These results suggest that the enhanced resistance to collapse results from enlargement by the additional material of the ordered phase.

摘要

在呼气时,肺泡表面积缩小会对肺表面活性物质产生压缩,使其降低表面张力,达到使表面活性物质单层从表面坍塌的水平。添加到这些单层下面的肺表面活性物质小泡会减缓坍塌。此处的 X 射线散射确定了添加的小泡所引起的结构变化。对提取的小牛肺表面活性剂单层进行掠入射 X 射线衍射检测到有序相。二棕榈酰磷脂酰胆碱和胆固醇的混合物,但不是单独的磷脂,可以模拟该结构。在稳定单层的浓度下,亚相中的小泡对单位晶胞没有影响,X 射线反射表明该膜仍然是单分子的。然而,添加的小泡会导致衍射强度的浓度依赖性增加。这些结果表明,增强的抗坍塌能力是由于额外物质使有序相扩大所致。