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大豆 7S 球蛋白肽与细胞膜模型的相互作用通过等温滴定量热法、石英晶体微量天平耗散和 Langmuir 单层研究。

Interaction of Soybean 7S Globulin Peptide with Cell Membrane Model via Isothermal Titration Calorimetry, Quartz Crystal Microbalance with Dissipation, and Langmuir Monolayer Study.

机构信息

Food Protein Research and Development Center, Guangdong Province Key Laboratory for Green Processing of Natural Products and Product Safety , South China University of Technology , Guangzhou 510640 , P. R China.

出版信息

J Agric Food Chem. 2018 May 16;66(19):4913-4922. doi: 10.1021/acs.jafc.8b00414. Epub 2018 Apr 13.

DOI:10.1021/acs.jafc.8b00414
PMID:29634259
Abstract

To understand the underlying molecular mechanism of the cholesterol-lowering effect of soybean 7S globulins, the interactions of their pepsin-released peptides (7S-peptides) with cell membrane models consisting of dipalmitoylphosphatidylcholine (DPPC), dioleoylphosphatidylcholine (DOPC), and cholesterol (CHOL) were systematically studied. The results showed that 7S-peptides were bound to DPPC/DOPC/CHOL liposomes mainly through van der Waals forces and hydrogen bonds, and the presence of higher CHOL concentrations enhanced the binding affinity (e.g., DPPC/DOPC/CHOL = 1:1:0, binding ratio = 0.114; DPPC/DOPC/CHOL = 1:1:1, binding ratio = 2.02). Compression isotherms indicated that the incorporation of 7S-peptides increased the DPPC/DOPC/CHOL monolayer fluidity and the lipid raft size. The presence of CHOL accelerated the 7S-peptide accumulation on lipid rafts, which could serve as platforms for peptides to develop into β-sheet rich structures. These results allow us to hypothesize that 7S-peptides may indirectly influence membrane protein functions via altering the membrane organization in the enterocytes.

摘要

为了理解大豆 7S 球蛋白降低胆固醇作用的潜在分子机制,系统研究了其胃蛋白酶释放肽(7S-肽)与由二棕榈酰磷脂酰胆碱(DPPC)、二油酰基磷脂酰胆碱(DOPC)和胆固醇(CHOL)组成的细胞膜模型的相互作用。结果表明,7S-肽主要通过范德华力和氢键与 DPPC/DOPC/CHOL 脂质体结合,较高的 CHOL 浓度增强了结合亲和力(例如,DPPC/DOPC/CHOL = 1:1:0,结合比 = 0.114;DPPC/DOPC/CHOL = 1:1:1,结合比 = 2.02)。压缩等温线表明,7S-肽的掺入增加了 DPPC/DOPC/CHOL 单层的流动性和脂筏的大小。CHOL 的存在加速了 7S-肽在脂筏上的积累,这可以作为肽形成富含β-折叠结构的平台。这些结果使我们假设 7S-肽可能通过改变肠细胞中的膜组织间接影响膜蛋白的功能。

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