Construction of AgrC Proteoliposomes by Detergent-Mediated Method
文献类型：期刊论文
| 作者 | Wang Lina1; Quan Chunshan2,3,4; Xu Yongbin2,3,4; Li Xihui2,3; Qu Xiaojing2,3,4; Fan Shengdi2,3,4 |
| 刊名 | acta chimica sinica
 |
| 出版日期 | 2014-02-15 |
| 卷号 | 72期号:2页码:233-240 |
| 关键词 | Staphylococcus aureus AgrC detergent proteoliposome membrane protein |
| 英文摘要 | to respond appropriately to different environmental changes, bacteria have evolved two-component signal transduction systems (tcsts), which are absent in mammals (including human beings). a typical tcst consisted of a sensor kinase (histidine kinase, hk) and a response regulator (rr). hk is capable of autophosphorylation in response to an environmental signal, while rr interacts with the phosphorylated hk. membrane protein agrc is a sensor kinase of a tcst from staphylococcus aureus. illumination of signal transduction mechanism is of great significance to solve the problem of bacterial resistance. at present, the main bottleneck of membrane protein is the difficulties in obtaining large quantities of sufficiently pure and functional protein. the target protein was overexpressed in escherichia coli, solubilized from cell membranes and purified in detergent micelles. this series of steps tend to lead to destabilizations of membrane protein and loss of function. in this study, agrc was incorporated into liposomes by a detergent-mediated method. for standard incorporation, protein solution was added to detergent-lipid suspension containing lipid at 2.5 mmol/l at a lipid-to-protein ratio of 300 (mol/mol). for slow detergent removal, successive additions of small amounts of beads at bio-bead-to-detergent ratios of 2 (w/w) will allow the removal of the detergent, resulting in formation of proteoliposome. the structure, morphology and average diameter of liposomes and proteoliposomes were characterized by transmission electron microscopy (tem) and dynamic light scattering (dls), respectively. sucrose density gradient centrifugation was employed to separate proteoliposomes. the result showed efficiency of protein incorporation and liposomes recovery reached 80% and 90%, respectively. thiol reagent labeling test showed the cytoplasmic domain of agrc was almost exclusively oriented towards the inside of the liposome vesicles. in vitro phosphorylation experiments showed that kinase activity of agrc in proteoliposomes was significantly higher than in detergent micelles. proteoliposomes could be stored for two weeks with little loss of function. preparation of proteoliposome not only solves the instability problem of membrane proteins, but also provides a new approach of the study of membrane protein structure, function and signal transduction mechanism in vitro. |
| WOS标题词 | science & technology ; physical sciences |
| 类目[WOS] | chemistry, multidisciplinary |
| 研究领域[WOS] | chemistry |
| 关键词[WOS] | histidine protein-kinase ; staphylococcus-aureus infections ; signal-transduction ; membrane-proteins ; receptor ; prediction ; topology ; virulence ; system ; reconstitution |
| 收录类别 | SCI |
| 语种 | 英语 |
| WOS记录号 | WOS:000333500600011 |
| 公开日期 | 2016-05-09 |
| 源URL | [http://cas-ir.dicp.ac.cn/handle/321008/145570]  |
| 专题 | 大连化学物理研究所_中国科学院大连化学物理研究所 |
| 作者单位 | 1.Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China 2.Dalian Nationalities Univ, State Ethn Affairs Commiss, Key Lab Biotechnol & Resource Utilizat, Dalian 116600, Peoples R China 3.Dalian Nationalities Univ, Minist Educ, Dalian 116600, Peoples R China 4.Dalian Nationalities Univ, Dept Life Sci, Dalian 116600, Peoples R China |
| 推荐引用方式 GB/T 7714 | Wang Lina,Quan Chunshan,Xu Yongbin,et al. Construction of AgrC Proteoliposomes by Detergent-Mediated Method[J]. acta chimica sinica,2014,72(2):233-240. |
| APA | Wang Lina,Quan Chunshan,Xu Yongbin,Li Xihui,Qu Xiaojing,&Fan Shengdi.(2014).Construction of AgrC Proteoliposomes by Detergent-Mediated Method.acta chimica sinica,72(2),233-240. |
| MLA | Wang Lina,et al."Construction of AgrC Proteoliposomes by Detergent-Mediated Method".acta chimica sinica 72.2(2014):233-240. |
入库方式： OAI收割
来源：大连化学物理研究所
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