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通过热异构化确定携带螺吡喃的蜂毒肽片段在磷脂双分子层膜中的位置。

Location of melittin fragment carrying spiropyran in phospholipid bilayer membrane determined by thermal isomerization.

作者信息

Kato E, Ueda T, Kimura S, Imanishi Y

机构信息

Department of Polymer Chemistry, Kyoto University, Japan.

出版信息

Biophys Chem. 1994 Apr;49(3):215-22. doi: 10.1016/0301-4622(93)e0071-c.

Abstract

Melittin fragments carrying spiropyran were synthesized, and their distribution in phospholipid bilayer membrane was studied by using spiropyran as a probe. Spiropyran was connected to the side chain of a Glu residue (Glu(OSp)), and the residue was replaced for the fourth position of melittin (1-7) fragment (M7Sp). M7Sp showed a high affinity for phospholipid membrane. The spiropyran group of M7Sp was converted to a merocyanin group by UV irradiation, which reduced the amount of the peptide bound to the membrane to the half of the initial amount. The location of the merocyanin group of M7Sp in the membrane was evaluated by the rate of thermal isomerization from merocyanin to spiropyran, which is sensitive to the microenvironment of merocyanin. A large fraction of the merocyanin group isomerized rapidly back to a spiropyran form, indicating that M7Sp is located in a relatively hydrophobic region of the membrane. Although the interaction of the peptide with phospholipid membrane is affected by photoisomerization of the spiropyran substituent, spiropyran was shown to be a useful tool to evaluate the location of the peptide in the lipid membrane.

摘要

合成了携带螺吡喃的蜂毒素片段,并以螺吡喃为探针研究了它们在磷脂双分子层膜中的分布。螺吡喃连接到谷氨酸残基(Glu(OSp))的侧链上,该残基取代了蜂毒素(1-7)片段(M7Sp)的第四个位置。M7Sp对磷脂膜表现出高亲和力。通过紫外线照射,M7Sp的螺吡喃基团转化为部花青基团,这使得与膜结合的肽量减少到初始量的一半。通过部花青向螺吡喃的热异构化速率来评估M7Sp的部花青基团在膜中的位置,该速率对部花青的微环境敏感。大部分部花青基团迅速异构化回螺吡喃形式,表明M7Sp位于膜的相对疏水区域。尽管肽与磷脂膜的相互作用受螺吡喃取代基的光异构化影响,但螺吡喃被证明是评估肽在脂质膜中位置的有用工具。

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