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脑突触的表面抗原:使用多克隆抗血清鉴定次要蛋白质。

Surface antigens of brain synapses: identification of minor proteins using polyclonal antisera.

作者信息

Matus A, Ng M, Pehling G, Ackermann M, Hauser K

出版信息

J Cell Biol. 1984 Jan;98(1):237-45. doi: 10.1083/jcb.98.1.237.

Abstract

Antigenic proteins of brain synaptic plasma membranes (SPM) and postsynaptic densities (PSD) were characterized using antisera raised against SPM. Immunostaining of brain sections showed that the antigens were restricted to synapses, and electron microscopy revealed staining at both presynaptic terminals and PSDs. In primary brain cell cultures the antisera were also neuron-specific but the antigens were distributed throughout the entire neuronal plasma membrane, suggesting that some restrictive influence present in whole tissue is absent when neurons are grown dispersed. The antigenic proteins with which these antisera react were identified using SDS gel immunoblots. SPM and PSD differed from one another in their characteristic antigenic proteins. Comparison with amido-black stained gel blots showed that in both cases most of these did not correspond to known abundant proteins of SPM or PSDs revealed by conventional biochemical techniques. None of the antigens revealed by the polyclonal antisera were detected by any of a large series of monoclonal antibodies against SPM.

摘要

利用针对脑突触质膜(SPM)产生的抗血清对脑突触质膜和突触后致密物(PSD)的抗原蛋白进行了表征。脑切片的免疫染色显示,这些抗原局限于突触,电子显微镜显示在突触前终末和突触后致密物处均有染色。在原代脑细胞培养物中,抗血清也是神经元特异性的,但抗原分布在整个神经元质膜上,这表明当神经元分散生长时,全组织中存在的一些限制性影响不存在了。使用SDS凝胶免疫印迹法鉴定了与这些抗血清反应的抗原蛋白。SPM和PSD在其特征性抗原蛋白方面彼此不同。与酰胺黑染色的凝胶印迹比较表明,在这两种情况下,其中大多数与传统生化技术揭示的SPM或PSD的已知丰富蛋白不对应。多克隆抗血清揭示的抗原均未被一系列针对SPM的单克隆抗体检测到。

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Monoclonal antibodies identify novel neural antigens.
Proc Natl Acad Sci U S A. 1982 Apr;79(7):2410-4. doi: 10.1073/pnas.79.7.2410.

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