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使用突触结合蛋白I的C2A结构域检测细胞凋亡。

Detection of apoptosis using the C2A domain of synaptotagmin I.

作者信息

Jung Hyo-Il, Kettunen Mikko I, Davletov Bazbek, Brindle Kevin M

机构信息

Department of Biochemistry, University of Cambridge, Tennis Court Road, Cambridge CB2 1GA, UK.

出版信息

Bioconjug Chem. 2004 Sep-Oct;15(5):983-7. doi: 10.1021/bc049899q.

Abstract

Binding of annexin V or the C2A domain of synaptotagmin I to phosphatidylserine expressed on the surface of apoptotic cells can, when labeled with appropriate probe molecules, be used to detect the presence of apoptosis using radionuclide, magnetic resonance, and optical imaging techniques. The preparation of a biotinylated C2A-GST fusion protein is described, and its capability, when used in conjunction with fluorescein-labeled streptavidin, of detecting apoptotic cells by flow cytometry is compared directly with the performance of a commercial preparation of fluorescein-labeled annexin V. Biotinylated C2A-GST, when used in conjunction with streptavidin-conjugated superparamagnetic iron oxide nanoparticles or Gd-chelate-avidin conjugates, was shown to be capable of detecting apoptotic cells using T(2)-weighted or T(1)-weighted magnetic resonance imaging experiments, respectively.

摘要

膜联蛋白V或突触结合蛋白I的C2A结构域与凋亡细胞表面表达的磷脂酰丝氨酸结合,当用适当的探针分子标记时,可利用放射性核素、磁共振和光学成像技术来检测凋亡的存在。本文描述了生物素化的C2A-GST融合蛋白的制备,并将其与荧光素标记的链霉亲和素结合使用时通过流式细胞术检测凋亡细胞的能力,与荧光素标记的膜联蛋白V的商业制剂的性能进行了直接比较。结果表明,生物素化的C2A-GST与链霉亲和素偶联的超顺磁性氧化铁纳米颗粒或钆螯合物-抗生物素蛋白偶联物结合使用时,分别能够通过T2加权或T1加权磁共振成像实验检测凋亡细胞。

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