维普中文期刊产品整合服务
27篇 您的检索式:作者名="Brunati"
    题名 作者 年代 出处 被引量
1Regulation of membrane band 3 Tyr-phosphorylation by proteolysis of p72^syk and possible involvement in senescence process显示文摘红血球老朽被房间表面 epitopes 的暴露在导致红血房间的有免疫力的调停的移动的房间膜蛋白质上描绘。为抗原形成的一机制是 transmembrane 蛋白质的酷氨酸 phosphorylation (Tyr-P ) 由 Syk kinase 的乐队 3。我们的目的是测试假设由到 isoform 提高的 36 kDa (p36Syk ) 的从 72 kDa (p72Syk ) 的变换的 Syk kinase 的那解朊的激活它的 phosphorylating 活动独立于有细胞骨架的 Syk kinase 的协会。Tyr-P 试金用 32P 举起的 quantification 被进行进在 p72Syk 或 p36Syk 的增加以后的乐队 3 的细胞质的领域。由调停 p72Syk 的 phosphorylation 上的 p36Syk 的红血球膜乐队 3 蛋白质的 pre-phosphorylation 的效果和调停 p72Syk 的 phosphorylation 上的一个朊酶禁止者(leupeptin ) 的增加的效果被 32P 举起的 autoradiographic 可视化学习。由骨胳的膜和乐队 3 的可溶的部分的 Syk isoforms 的 Tyr-P 被 immunoblotting 设想。p36Syk 有一个更高级的乐队,这被发现 3 酷氨酸 phosphorylating 活动与 p72Syk 相比。有 p36Syk 或 p72Syk 的 Pre-phosphorylation 增加了乐队 3 phosphorylating 活动。朊酶抑制处理显著地减少了 p72Syk 然而并非 p36Syk 乐队 3 酷氨酸 phosphorylating 活动。可溶并且乐队 3 蛋白质的骨胳的部分是的膜同等地由每 Syk isoform 的酷氨酸 phosphorylated。在结论,我们证实了 p72Syk 的解朊的劈开是为乐队 3 Tyr-P 和它与细胞骨架的乐队 3 的协会的独立的重要的规章的步的假设。Luciana Bordin Cristina Fiore Marcantonio Bragadin Anna Maria Brunati Giulio Clari 2009Acta Biochimica et Biophysica Sinica2009,41,10:3
2Viral proteins and Src family kinases: Mechanisms of pathogenicity from a “liaison dangereuse”显示文摘To complete their life cycle and spread, viruses interfere with and gain control of diverse cellular processes, this most often occurring through interaction between viral proteins(VPs) and resident protein partners. Among the latter, Src family kinases(SFKs), a class of non-receptor tyrosine kinases that contributes to the conversion of extracellular signals into intracellular signaling cascades and is involved in virtually all cellular processes, have recently emerged as critical mediators between the cell's infrastructure and the viral demands. In this scenario, structural or ex novo synthesized VPs are able to bind to the different domains of these enzymes through specific short linear motifs present along their sequences. Proline-rich motifs displaying the conserved minimal consensus PxxP and recognizing the SFK Src homology(SH)3 domain constitute a cardinal signature for the formation of multiprotein complexes and this interaction may promote phosphorylation of VPs by SFKs, thus creating phosphotyrosine motifs that become a docking site for the SH2 domains of SFKs or other SH2 domain-bearing signaling molecules. Importantly, the formation of these assemblies also results in a change in the activity and/or location of SFKs, and these events are critical in perturbing key signalingpathways so that viruses can utilize the cell's machinery to their own benefit. In the light of these observations, although VPs as such, especially those with enzyme activity, are still regarded as valuable targets for therapeutic strategies, multiprotein complexes composed of viral and host cell proteins are increasingly becoming objects of investigation with a view to deeply characterize the structural aspects that favor their formation and to develop new compounds able to contrast viral diseases in an alternative manner.Mario Angelo Pagano Elena Tibaldi Giorgio Palù Anna Maria Brunati 2013World Journal of Virology2013,2,2:3
3Biotrans- formations of cinnamic and ferulic acid with Actinomycetes显示文摘Brunati M Marinelli F Bertolini C 2004Enzyme and Microbial Technology2004,34,1:1
4Crucial role of HsPg0 in the Akt-dependent promotion of angiogenic-like effect of glucose-regulated protein94 ( Grp94 ) -IgG complexes显示文摘Tramentozzi E Tibaldi E Brunati AM 2011J Cell Mol Meal2011,15,12:1
5Mycophenolate mofetil monotherapy in liver transplantation显示文摘Pierini A Mirabella S Brunati A 2005Transplant Proc2005,37,6:1
6Small bowel capsule endoscopy in clinical practice: a multicenter 7-year survey显示文摘Emanuele Rondonotti Marco Soncini Carlo Girelli Giovanni Ballardini Guglielmo Bianchi Sergio Brunati Laura Centenara Pietro Cesari Claudio Cortelezzi Simona Curioni Claudio Gozzini Renzo Gullotta Marco Lazzaroni Marta Maino Giovanna Mandelli Nicola Mantov 2010European Journal of Gastroenterology & Hepatology2010,,11:1
7Functional VEGF and VEGF receptors are expressed in human medulloblastomas 显示文摘Slongo M L Molena B Brunati A M 2007Neuro Oncol2007,9,:1
8Functional VEGF and VEGF receptors are expressed in human medulloblastomas 显示文摘Slongo ML Molena B Brunati AM 2007Neuro Oncol2007,9,4:1
9Ser/Thr phosphorylation of hematopoietic specific protein 1 (HSI) 显示文摘Ruzzene M Brunati AM Sarno S 2000Eur J Biochem2000,267,:1
10Functional VEGF and VEGF receptors are expressed in human medulloblastomas显示文摘Slongo ML Molena B Brunati AM 2007Neuro Oncol2007,9,4:1
11Diagnosis of bacteriuria and leukocyturia by automated flow cytometry compared with urine culture显示文摘Piertti B Brunati P Pini B 2010J Clin Microbiol2010,48,11:1
12Thrombin-induced tyrosine phosphorylation of HS1 in human platelets is sequentially catalyzed by Syk and Lyn tyrosine kinases and associated with the cellular migration of the protein显示文摘Brunati AM Deana R Folda A 2005J Biol Chem2005,280,21:1
13Diagnosis of bacteriuria and leu- kocyturia by automated flow cytometry compared with urine cul- ture显示文摘Pieretti B Brunati P Pini B 2010J Clin Microbiol2010,48,11:1
14Biotransformations of cinnamic and ferulic acid with actinomycetes显示文摘Mara Brunati Flavia Marinelli Cristina Bertolini 2004Enzyme and Microbial Technology2004,34,:1
15Functional VEGF and VEGF receptors are expressed in human medulloblastomas显示文摘Slongo M L Molena B Brunati A M Frasson M Gardiman M Carli M Perilongo G Rosolen A 0,,04:1
16Thiol redox systems and protein kinases in hepatic atellate cell regulatory processes显示文摘Brunati AM Pagano MA Bindoli A 2010Free Radic Res2010,44,4:1
17Small bowel capsule endoscopy in clinical practice: a multicenter 7-year survey显示文摘Emanuele Rondonotti Marco Soncini Carlo Girelli Giovanni Ballardini Guglielmo Bianchi Sergio Brunati Laura Centenara Pietro Cesari Claudio Cortelezzi Simona Curioni Claudio Gozzini Renzo Gullotta Marco Lazzaroni Marta Maino Giovanna Mandelli Nicola Mantov 2010European Journal of Gastroenterology & Hepatology2010,,11:1
18Thiol redox systems and protein kinases in hepatic stellate cell regulatory processes显示文摘Brunati AM Pagano MA Bindoli A et a7 2010Free RadicRes2010,44,:1
19New-onset diabetes af- ter liver transplantation显示文摘Mirabella S Brunati A Rieehiuti A 2005Transplant Proc2005,37,6:1
20The SH3 domain of HS1 protein recognizes lysine-rich polyproline motifs显示文摘Giuliano Siligardi Paolo Ruzza Rohanah Hussain Luca Cesaro Anna Maria Brunati Lorenzo A. Pinna Arianna Donella-Deana 2012Amino Acids2012,,4:1
返回顶部 每页显示:
共2页 首页 上一页 第1页 下一页 末页 /2 跳转

网站首页 | 关于我们 | 联系我们 | 产品服务 | 客服中心 | 广告服务 | 版权声明 | 网站联盟 | 友情链接 | 售卡网点

版权所有© 渝B2-20050021-1 渝公网安备 50019002500403号 违法和不良信息举报中心

互联网出版许可证 新出网证(渝)字10号 全国400电话 - 免长途话费