• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

非均相体系中血卟啉和血卟啉衍生物平衡的研究。卟啉-脂质体结合及卟啉在水中的二聚作用。

Studies of hematoporphyrin and hematoporphyrin derivative equilibria in heterogeneous systems. Porphyrin-liposome binding and porphyrin aqueous dimerization.

作者信息

Margalit R, Cohen S

出版信息

Biochim Biophys Acta. 1983 Dec 21;736(2):163-70. doi: 10.1016/0005-2736(83)90280-8.

DOI:10.1016/0005-2736(83)90280-8
PMID:6228253
Abstract

Two processes of porphyrins in heterogeneous systems containing aqueous and membrane phases have been studied with hematoporphyrin and hematoporphyrin derivative: Dimerization equilibrium in the aqueous phases and porphyrin-membrane binding equilibrium using liposomes as models for biological membranes. The interrelationship of aqueous aggregations and membrane binding was probed and the porphyrin aggregation state in the membrane, at equilibrium, was assessed. Fluorimetric techniques were employed. The dimerization equilibrium constants, at neutral pH and 37 degrees C were found to be 2.8 X 10(5) M-1 and 1.9 X 10(6) M-1 for hematoporphyrin and its derivative, respectively. Over a porphyrin concentration range going from monomer-dominant to dimer-dominant systems, we have found that only monomers are bound to the membrane. The respective monomer-liposome binding constants, found to be independent of the initial monomer/dimer distribution in the aqueous phase, were determined to be 1.6 X 10(3) M-1 and 4.1 X 10(3) M-1 at neutral pH and 37 degrees C for hematoporphyrin and its derivative, respectively. The monomer-liposome interaction was found to perurb the initial monomer/dimer distribution in the aqueous phase, so that the monomers residing at equilibrium in the membrane originate from both monomers and dimers in the aqueous phase.

摘要

利用血卟啉和血卟啉衍生物,研究了在含有水相和膜相的非均相体系中卟啉的两个过程:水相中的二聚化平衡以及使用脂质体作为生物膜模型的卟啉 - 膜结合平衡。探讨了水相聚集与膜结合之间的相互关系,并评估了平衡时膜中卟啉的聚集状态。采用了荧光技术。在中性pH和37℃条件下,血卟啉及其衍生物的二聚化平衡常数分别为2.8×10⁵ M⁻¹和1.9×10⁶ M⁻¹。在从单体主导体系到二聚体主导体系的卟啉浓度范围内,我们发现只有单体与膜结合。在中性pH和37℃条件下,血卟啉及其衍生物各自的单体 - 脂质体结合常数分别为1.6×10³ M⁻¹和4.1×10³ M⁻¹,且发现其与水相中初始单体/二聚体分布无关。发现单体 - 脂质体相互作用会扰乱水相中初始单体/二聚体分布,因此平衡时存在于膜中的单体既来源于水相中的单体,也来源于水相中的二聚体。

相似文献

1
Studies of hematoporphyrin and hematoporphyrin derivative equilibria in heterogeneous systems. Porphyrin-liposome binding and porphyrin aqueous dimerization.非均相体系中血卟啉和血卟啉衍生物平衡的研究。卟啉-脂质体结合及卟啉在水中的二聚作用。
Biochim Biophys Acta. 1983 Dec 21;736(2):163-70. doi: 10.1016/0005-2736(83)90280-8.
2
Binding of hematoporphyrin derivative to membranes. Expression of porphyrin heterogeneity and effects of cholesterol studied in large unilamellar liposomes.
Biochim Biophys Acta. 1985 Mar 14;813(2):307-12. doi: 10.1016/0005-2736(85)90246-9.
3
Porphyrin-membrane interactions: binding or partition?
Biochim Biophys Acta. 1987 Nov 27;905(1):173-80. doi: 10.1016/0005-2736(87)90021-6.
4
Studies on the solvophobic nature of porphyrin self aggregation vs. the lipophylic nature of porphyrin-membrane binding.关于卟啉自聚集的疏溶剂性质与卟啉 - 膜结合的亲脂性质的研究。
Adv Exp Med Biol. 1985;193:303-11. doi: 10.1007/978-1-4613-2165-1_29.
5
Physicochemical studies of processes involving potential photodynamic drugs on route to their targets: self-aggregation and membrane-binding of Zn-hematoporphyrin.涉及潜在光动力药物到达其靶点过程的物理化学研究:锌血卟啉的自聚集和膜结合
Arch Biochem Biophys. 1986 May 15;247(1):57-61. doi: 10.1016/0003-9861(86)90532-1.
6
Temperature-induced changes in fluorescence properties as a probe of porphyrin microenvironment in lipid membranes. 2. The partition of hematoporphyrin and protoporphyrin in mitochondria.温度诱导的荧光特性变化作为脂质膜中卟啉微环境的探针。2. 血卟啉和原卟啉在线粒体中的分配。
Eur J Biochem. 1995 Oct 1;233(1):165-70. doi: 10.1111/j.1432-1033.1995.165_1.x.
7
Fluorimetric studies on the dimerization equilibrium of protoporphyrin IX and its haemato derivative.原卟啉IX及其血红素衍生物二聚化平衡的荧光研究。
Biochem J. 1983 Feb 1;209(2):547-52. doi: 10.1042/bj2090547.
8
Porphyrin-membrane interactions: structural, kinetic and thermodynamic aspects studied using fluorescence techniques.卟啉-膜相互作用:运用荧光技术研究其结构、动力学及热力学方面
Adv Exp Med Biol. 1985;193:169-80. doi: 10.1007/978-1-4613-2165-1_20.
9
Effects of membrane physical parameters on hematoporphyrin-derivative binding to liposomes: a spectroscopic study.
J Membr Biol. 1987;97(3):215-21. doi: 10.1007/BF01869224.
10
The partition and distribution of porphyrins in liposomal membranes. A spectroscopic study.卟啉在脂质体膜中的分配与分布:一项光谱学研究
Biochim Biophys Acta. 1989 Jul 24;983(1):118-22. doi: 10.1016/0005-2736(89)90388-x.

引用本文的文献

1
Photophysical Properties of Protoporphyrin IX, Pyropheophorbide-a and Photofrin in Different Conditions.原卟啉IX、焦脱镁叶绿酸-a及光卟啉在不同条件下的光物理性质
Pharmaceuticals (Basel). 2021 Feb 9;14(2):138. doi: 10.3390/ph14020138.
2
Design and synthesis of a 4-aminoquinoline-based molecular tweezer that recognizes protoporphyrin IX and iron(iii) protoporphyrin IX and its application as a supramolecular photosensitizer.一种基于4-氨基喹啉的分子钳的设计与合成,该分子钳可识别原卟啉IX和铁(III)原卟啉IX及其作为超分子光敏剂的应用。
Chem Sci. 2018 Aug 31;9(38):7455-7467. doi: 10.1039/c8sc02133c. eCollection 2018 Oct 14.
3
A new nanoconstruct for epidermal growth factor receptor-targeted photo-immunotherapy of ovarian cancer.
一种用于表皮生长因子受体靶向光免疫治疗卵巢癌的新型纳米构建体。
Nanomedicine. 2013 Oct;9(7):1114-22. doi: 10.1016/j.nano.2013.02.005. Epub 2013 Feb 26.
4
Thermodynamics of porphyrin dimerization in aqueous solutions.水溶液中卟啉二聚化的热力学
Biochem J. 1984 Apr 15;219(2):445-50. doi: 10.1042/bj2190445.
5
Deuteroporphyrin-albumin binding equilibrium. The effects of porphyrin self-aggregation studied for the human and the bovine proteins.次卟啉 - 白蛋白结合平衡。针对人源和牛源蛋白质研究了卟啉自聚集的影响。
Biochem J. 1985 Jul 1;229(1):197-203. doi: 10.1042/bj2290197.
6
Binding of porphyrin to human serum albumin. Structure-activity relationships.卟啉与人血清白蛋白的结合。构效关系。
Biochem J. 1990 Sep 1;270(2):325-30. doi: 10.1042/bj2700325.