细胞与分子免疫学杂志
細胞與分子免疫學雜誌
세포여분자면역학잡지
2009年
10期
870-874
,共5页
徐忠伟%徐瑞成%陈小义%刘英富
徐忠偉%徐瑞成%陳小義%劉英富
서충위%서서성%진소의%류영부
哇巴因%噬菌体展示肽库%结合肽%血管内皮细胞%细胞死亡%钠泵亚单位
哇巴因%噬菌體展示肽庫%結閤肽%血管內皮細胞%細胞死亡%鈉泵亞單位
왜파인%서균체전시태고%결합태%혈관내피세포%세포사망%납빙아단위
ouabain%phage display peptide library%conjugated peptide%vascular endothelial cell%cell death%Na~+-K~+-ATPase subunit
目的:寻找与哇巴因高亲和力结合并抑制其生物功能的相关小分子肽,为治疗原发性高血压提供新策略.方法:以哇巴因为筛选分子,应用M13噬菌体呈现随机7肽库进行筛选.经过3轮生物淘筛,并通过ELISA法鉴定,对噬菌体阳性克隆ssDNA电泳鉴定和基因测序分析.委托合成筛选获得哇巴因结合肽,采用放射配基受体结合法检测其结合活性;MTT法检测血管内皮细胞的增殖抑制率,Hoechst33342/PI双荧光染色检测细胞形态学变化;利用RT-PCR和细胞免疫荧光检测钠泵α1、β1的表达水平;荧光探针检测细胞内游离Na+浓度变化.结果:筛选获得14个阳性克隆,基因测序显示:哇巴因结合肽一致率达64.3%(9/14).委托合成肽(Arg-Cys-Met-Thr-Ser-Arg-Ser).放射性配基受体结合法检测显示,合成的哇巴因结合肽能够与哇巴因结合.哇巴因结合肽+哇巴因的EAhy926细胞组增殖抑制率小于哇巴因组(P<0.05);Hoechst33342/PI双荧光染色显示细胞死亡数量减少;RT-PCR和免疫细胞化学检测钠泵α1、β1亚单位转录和翻译水平,显示哇巴因结合肽能拈抗哇巴因所引起钠泵α1亚单位表达的上调、β1亚单位的下调作用;荧光探针显示哇巴因结合肽能够拮抗哇巴因对钠泵的抑制作用.结论:哇巴因特异性结合肽能够阻抑哇巴因对血管内皮细胞的抑制增殖和诱导死亡作用,为研究哇巴因与钠泵的相互作用机制及进一步研究抗哇巴因的分子药物奠定基础.
目的:尋找與哇巴因高親和力結閤併抑製其生物功能的相關小分子肽,為治療原髮性高血壓提供新策略.方法:以哇巴因為篩選分子,應用M13噬菌體呈現隨機7肽庫進行篩選.經過3輪生物淘篩,併通過ELISA法鑒定,對噬菌體暘性剋隆ssDNA電泳鑒定和基因測序分析.委託閤成篩選穫得哇巴因結閤肽,採用放射配基受體結閤法檢測其結閤活性;MTT法檢測血管內皮細胞的增殖抑製率,Hoechst33342/PI雙熒光染色檢測細胞形態學變化;利用RT-PCR和細胞免疫熒光檢測鈉泵α1、β1的錶達水平;熒光探針檢測細胞內遊離Na+濃度變化.結果:篩選穫得14箇暘性剋隆,基因測序顯示:哇巴因結閤肽一緻率達64.3%(9/14).委託閤成肽(Arg-Cys-Met-Thr-Ser-Arg-Ser).放射性配基受體結閤法檢測顯示,閤成的哇巴因結閤肽能夠與哇巴因結閤.哇巴因結閤肽+哇巴因的EAhy926細胞組增殖抑製率小于哇巴因組(P<0.05);Hoechst33342/PI雙熒光染色顯示細胞死亡數量減少;RT-PCR和免疫細胞化學檢測鈉泵α1、β1亞單位轉錄和翻譯水平,顯示哇巴因結閤肽能拈抗哇巴因所引起鈉泵α1亞單位錶達的上調、β1亞單位的下調作用;熒光探針顯示哇巴因結閤肽能夠拮抗哇巴因對鈉泵的抑製作用.結論:哇巴因特異性結閤肽能夠阻抑哇巴因對血管內皮細胞的抑製增殖和誘導死亡作用,為研究哇巴因與鈉泵的相互作用機製及進一步研究抗哇巴因的分子藥物奠定基礎.
목적:심조여왜파인고친화력결합병억제기생물공능적상관소분자태,위치료원발성고혈압제공신책략.방법:이왜파인위사선분자,응용M13서균체정현수궤7태고진행사선.경과3륜생물도사,병통과ELISA법감정,대서균체양성극륭ssDNA전영감정화기인측서분석.위탁합성사선획득왜파인결합태,채용방사배기수체결합법검측기결합활성;MTT법검측혈관내피세포적증식억제솔,Hoechst33342/PI쌍형광염색검측세포형태학변화;이용RT-PCR화세포면역형광검측납빙α1、β1적표체수평;형광탐침검측세포내유리Na+농도변화.결과:사선획득14개양성극륭,기인측서현시:왜파인결합태일치솔체64.3%(9/14).위탁합성태(Arg-Cys-Met-Thr-Ser-Arg-Ser).방사성배기수체결합법검측현시,합성적왜파인결합태능구여왜파인결합.왜파인결합태+왜파인적EAhy926세포조증식억제솔소우왜파인조(P<0.05);Hoechst33342/PI쌍형광염색현시세포사망수량감소;RT-PCR화면역세포화학검측납빙α1、β1아단위전록화번역수평,현시왜파인결합태능념항왜파인소인기납빙α1아단위표체적상조、β1아단위적하조작용;형광탐침현시왜파인결합태능구길항왜파인대납빙적억제작용.결론:왜파인특이성결합태능구조억왜파인대혈관내피세포적억제증식화유도사망작용,위연구왜파인여납빙적상호작용궤제급진일보연구항왜파인적분자약물전정기출.
AIM: To find one kind of peptide that will conjugate with ouabain and inhibit its biological function, and provide a new treatment strategy for primary hypertension. METHODS: In this study, ouabain was used as a target to screen ouabain conjugated peptide (OCP) from Ph. D. -7 phage display peptide library. After 3 rounds of bio-panning, the products were identified by ELISA and DNA electrophoresis analysis and sequencing. Peptide was synthesized and analyzed the activity by radioligand binding assay. The inhibitory ratio of cell proliferation was measured by MTT and the cell morphology changing was measured by Hoechst 33342/PI staining. The expression of Na~+-K~+-ATPase α1-subunit and β1-subunit were detected by RT-PCR and immunocytochemistry. The levels of the free intracellular Na~+ in EAhy926 cells were measured by laser confocal microscope. RESULTS: The ouabain conjugated peptide was found out, and it was occupied in 0.64(9/14). The analysis of protein showed that the obtained peptides had no homology with Na~+-K~+-ATPase. The amino acid sequence of synthesized peptide was Arg-Cys-Met-Thr-Ser-Arg-Ser. There was binding activity between OCP and ~3H-ouabain. The MTT assay showed that OCP could reverse the inhibition action of ouabain on vascular endothelial EAhy926 cells in a dose and time-dependent manner. The number of apoptotic cells had significantly decreased detected by Hoechst 33342/PI staining. The results of RT-PCR and immunocytochemistry showed that OCP could inhibit the up-regulated expression of Na~+-K~+-ATPase α1-subunit and down-regulated expression of Na~+-K~+-ATPase β1-subunit induced by ouabain in EAhy926 cells. CONCLUSION: The OCP could reverse the growth inhibition and death induction of ouabain in EAhy926 cells, which would provide the basis for studying the interaction between ouabain and Na~+-K~+-ATPase and explore novel anti-ouabain agents.