{"title":"重组大鼠肝微粒体膜和含细胞色素5- orp -450蛋白脂质体的超微结构","authors":"V.L. Borovyagin , Yu.S. Tarachovsky , I.P. Kanaeva , A.V. Karyakin , G.I. Bachmanova , A.I. Archakov","doi":"10.1016/0889-1605(85)90085-0","DOIUrl":null,"url":null,"abstract":"<div><p>Thin sectioning and freeze-fracture electron microscopy have been used to show that it is possible to obtain topologically closed vesicles by means of reconstitution of rat liver microsomal membrane “ghosts.” The reconstitution by 15 hr dialysis resulted in the formation of vesicles with intra-membrane particles (IMP) while after 40 hr dialysis no IMP were observed in the membranes. The protein/lipid ratio and functional activity of NADPH- and NADH-linked enzyme systems were similar in both cases. Cytochrome<em>P</em>-450 (LM<sub>2</sub>) was incorporated into liposomes of different composition (protein : lipid ratio — 1:200). IMP were observed only when the incorporation of cytochrome P-450 was performed in the presence of detergent Emulgen 913 as specific additive to the initial protein-lipid-sodium cholate mixture or in the course of incubation of proteoliposomal suspensions at 37°C. After the incorporation of cytochrome<em>b<sub>5</sub></em> into azolectin liposomes vesicular membranes contain IMP if the incorporated membrane protein: lipid ratio is at least 1:50. Pronase-induced splitting off of a 11 kDa heme-containing fragment of cytochrome<em>b<sub>5</sub></em> did not affect IMP content. The conditions of IMP formation in reconstituted membranes and in microsomal ghosts are discussed.</p></div>","PeriodicalId":17593,"journal":{"name":"Journal of ultrastructure research","volume":"93 1","pages":"Pages 50-60"},"PeriodicalIF":0.0000,"publicationDate":"1985-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0889-1605(85)90085-0","citationCount":"4","resultStr":"{\"title\":\"Ultrastructure of reconstituted rat liver microsomal membranes and cytochromeb5- orP-450-containing proteoliposomes\",\"authors\":\"V.L. Borovyagin , Yu.S. Tarachovsky , I.P. Kanaeva , A.V. Karyakin , G.I. Bachmanova , A.I. Archakov\",\"doi\":\"10.1016/0889-1605(85)90085-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Thin sectioning and freeze-fracture electron microscopy have been used to show that it is possible to obtain topologically closed vesicles by means of reconstitution of rat liver microsomal membrane “ghosts.” The reconstitution by 15 hr dialysis resulted in the formation of vesicles with intra-membrane particles (IMP) while after 40 hr dialysis no IMP were observed in the membranes. The protein/lipid ratio and functional activity of NADPH- and NADH-linked enzyme systems were similar in both cases. Cytochrome<em>P</em>-450 (LM<sub>2</sub>) was incorporated into liposomes of different composition (protein : lipid ratio — 1:200). IMP were observed only when the incorporation of cytochrome P-450 was performed in the presence of detergent Emulgen 913 as specific additive to the initial protein-lipid-sodium cholate mixture or in the course of incubation of proteoliposomal suspensions at 37°C. After the incorporation of cytochrome<em>b<sub>5</sub></em> into azolectin liposomes vesicular membranes contain IMP if the incorporated membrane protein: lipid ratio is at least 1:50. Pronase-induced splitting off of a 11 kDa heme-containing fragment of cytochrome<em>b<sub>5</sub></em> did not affect IMP content. The conditions of IMP formation in reconstituted membranes and in microsomal ghosts are discussed.</p></div>\",\"PeriodicalId\":17593,\"journal\":{\"name\":\"Journal of ultrastructure research\",\"volume\":\"93 1\",\"pages\":\"Pages 50-60\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1985-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/0889-1605(85)90085-0\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of ultrastructure research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/0889160585900850\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of ultrastructure research","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0889160585900850","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Ultrastructure of reconstituted rat liver microsomal membranes and cytochromeb5- orP-450-containing proteoliposomes
Thin sectioning and freeze-fracture electron microscopy have been used to show that it is possible to obtain topologically closed vesicles by means of reconstitution of rat liver microsomal membrane “ghosts.” The reconstitution by 15 hr dialysis resulted in the formation of vesicles with intra-membrane particles (IMP) while after 40 hr dialysis no IMP were observed in the membranes. The protein/lipid ratio and functional activity of NADPH- and NADH-linked enzyme systems were similar in both cases. CytochromeP-450 (LM2) was incorporated into liposomes of different composition (protein : lipid ratio — 1:200). IMP were observed only when the incorporation of cytochrome P-450 was performed in the presence of detergent Emulgen 913 as specific additive to the initial protein-lipid-sodium cholate mixture or in the course of incubation of proteoliposomal suspensions at 37°C. After the incorporation of cytochromeb5 into azolectin liposomes vesicular membranes contain IMP if the incorporated membrane protein: lipid ratio is at least 1:50. Pronase-induced splitting off of a 11 kDa heme-containing fragment of cytochromeb5 did not affect IMP content. The conditions of IMP formation in reconstituted membranes and in microsomal ghosts are discussed.