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通过免疫电子显微镜对嘌呤霉素在大肠杆菌大核糖体亚基上结合位点的定位

Localization of the puromycin binding site on the large ribosomal subunit of Escherichia coli by immunoelectron microscopy.

作者信息

Lührmann R, Bald R, Stöffler-Meilicke M, Stöffler G

出版信息

Proc Natl Acad Sci U S A. 1981 Dec;78(12):7276-80. doi: 10.1073/pnas.78.12.7276.

Abstract

By using immunoelectron microscopy, we have localized the binding site on 50S Escherichia coli ribosomal subunits for puromycin, an antibiotic that interacts with the ribosomal peptidyltransferase center. This was achieved by affinity-labeling 50S subunits with N-bromoacetyl puromycin and treating the labeled subunits with an antibody specific for the N6,N6-dimethyladenosine moiety of puromycin. The position of the puromycin binding site was then revealed by localizing the attachment sites of the IgG molecules on the surfaces of the 50S subunits under the electron microscope: it was located at the interface between the subunits, on and around the wider lateral protuberance of the 50S subunit. This localizes directly the peptidyl transferase center on the surface of the large ribosomal subunit.

摘要

通过使用免疫电子显微镜,我们已将嘌呤霉素(一种与核糖体肽基转移酶中心相互作用的抗生素)在50S大肠杆菌核糖体亚基上的结合位点定位。这是通过用N-溴乙酰嘌呤霉素对50S亚基进行亲和标记,并使用对嘌呤霉素的N6,N6-二甲基腺苷部分具有特异性的抗体处理标记的亚基来实现的。然后通过在电子显微镜下定位IgG分子在50S亚基表面的附着位点来揭示嘌呤霉素结合位点的位置:它位于亚基之间的界面处,在50S亚基较宽的侧向突起上及其周围。这直接将肽基转移酶中心定位在大核糖体亚基的表面上。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21b0/349248/d6e1bafec583/pnas00663-0071-a.jpg

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