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用探针[3-(三氟甲基)-3-(间-[¹²⁵I]碘苯基)重氮甲烷]对中国仓鼠卵巢细胞的脂质进行放射性标记。

Radiolabeling of the lipids of chinese hamster ovary cells with the probe [3-(trifluoromethyl)-3-(m-[125I]iodophenyl)diazirine].

作者信息

Pérochon E, Leray C, Crémel G, Hubert P

机构信息

INSERM U. 338, 5 rue Blaise Pascal, Strasbourg, F67084, France.

出版信息

Anal Biochem. 1997 Dec 1;254(1):109-18. doi: 10.1006/abio.1997.2360.

Abstract

[125I]TID [3-(trifluoromethyl)-3-(m-[125I]iodophenyl)diazirine] is a commercially available, hydrophobic, photoactivatable, gamma-emitting reagent mostly used to label protein hydrophobic domains. It has also been used to radiolabel the phospholipids of lung surfactant (Gilliard et al., Anal. Biochem. 193, 310-315, 1991). Since a nonspecific, highly sensitive, lipid-labeling probe would be a very useful tool to investigate lipid-protein interactions in biological membranes, we characterized further the [125I]TID-labeling products of lipids from cultured Chinese hamster ovary cells (IR-CHO). After labeling of whole cells, TLC analysis followed by autoradiography enabled detection of sphingomyelin, phosphatidylcholine, phosphatidylinositol, phosphatidylserine, phosphatidylethanolamine, cardiolipin, diglycerides, cholesterol and its esters, and triglycerides. Analysis of the radioactivity associated with the saponification products of different lipids showed that [125I]TID was mostly (80%) extracted with the fatty acid moiety of the lipids whereas 20% remained associated with the hydrosoluble moiety. Similar radioactivity profiles were observed after labeling of whole cells or extracted and liposome-reconstituted lipids; the [125I]TID probe was able to diffuse in all intracellular organelles. Labeling was not equivalent between the different lipid classes, and it appeared that the amount of associated radioactivity correlated well with the degree of lipid unsaturation. This was confirmed by studying [125I]TID incorporation in phosphatidylcholines of different chain length and unsaturation. Taken together, our data demonstrate that [125I]TID can be used as a radiolabel for lipids in cultured cells. It is rapidly incorporated in the hydrophobic part of membranes, diffuses into all cellular compartments, and labels all lipid classes, including phospholipids, cholesterol, and glycerides, with a sensitivity in the nanomolar range.

摘要

[125I]TID [3-(三氟甲基)-3-(间-[125I]碘苯基)二氮杂环丙烷]是一种可商购的、疏水性的、光可激活的、发射γ射线的试剂,主要用于标记蛋白质疏水结构域。它也已被用于对肺表面活性剂的磷脂进行放射性标记(吉利德等人,《分析生物化学》193, 310 - 315, 1991)。由于一种非特异性的、高灵敏度的脂质标记探针将是研究生物膜中脂质 - 蛋白质相互作用的非常有用的工具,我们进一步对来自培养的中国仓鼠卵巢细胞(IR - CHO)的脂质的[125I]TID标记产物进行了表征。对全细胞进行标记后,通过薄层层析分析和放射自显影能够检测到鞘磷脂、磷脂酰胆碱、磷脂酰肌醇、磷脂酰丝氨酸、磷脂酰乙醇胺、心磷脂、甘油二酯、胆固醇及其酯类以及甘油三酯。对与不同脂质的皂化产物相关的放射性分析表明,[125I]TID大部分(80%)与脂质的脂肪酸部分一起被提取出来,而20%仍与水溶性部分相关。在对全细胞进行标记或对提取并重新构建脂质体的脂质进行标记后观察到了相似的放射性分布;[125I]TID探针能够扩散到所有细胞内细胞器中。不同脂质类别之间的标记并不相同,并且似乎相关放射性的量与脂质不饱和度程度密切相关。通过研究[125I]TID在不同链长和不饱和度的磷脂酰胆碱中的掺入情况证实了这一点。综上所述,我们的数据表明[125I]TID可作为培养细胞中脂质的放射性标记物。它能迅速掺入膜的疏水部分,扩散到所有细胞区室,并标记所有脂质类别,包括磷脂、胆固醇和甘油酯,灵敏度在纳摩尔范围内。

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