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桥粒斑蛋白的氨基末端结构域与桥粒珠蛋白结合,并使桥粒钙黏蛋白-桥粒珠蛋白复合物聚集。

The amino-terminal domain of desmoplakin binds to plakoglobin and clusters desmosomal cadherin-plakoglobin complexes.

作者信息

Kowalczyk A P, Bornslaeger E A, Borgwardt J E, Palka H L, Dhaliwal A S, Corcoran C M, Denning M F, Green K J

机构信息

Department of Dermatology, Northwestern University Medical School, Chicago, Illinois 60611, USA.

出版信息

J Cell Biol. 1997 Nov 3;139(3):773-84. doi: 10.1083/jcb.139.3.773.

Abstract

The desmosome is a highly organized plasma membrane domain that couples intermediate filaments to the plasma membrane at regions of cell-cell adhesion. Desmosomes contain two classes of cadherins, desmogleins, and desmocollins, that bind to the cytoplasmic protein plakoglobin. Desmoplakin is a desmosomal component that plays a critical role in linking intermediate filament networks to the desmosomal plaque, and the amino-terminal domain of desmoplakin targets desmoplakin to the desmosome. However, the desmosomal protein(s) that bind the amino-terminal domain of desmoplakin have not been identified. To determine if the desmosomal cadherins and plakoglobin interact with the amino-terminal domain of desmoplakin, these proteins were co-expressed in L-cell fibroblasts, cells that do not normally express desmosomal components. When expressed in L-cells, the desmosomal cadherins and plakoglobin exhibited a diffuse distribution. However, in the presence of an amino-terminal desmoplakin polypeptide (DP-NTP), the desmosomal cadherins and plakoglobin were observed in punctate clusters that also contained DP-NTP. In addition, plakoglobin and DP-NTP were recruited to cell-cell interfaces in L-cells co-expressing a chimeric cadherin with the E-cadherin extracellular domain and the desmoglein-1 cytoplasmic domain, and these cells formed structures that were ultrastructurally similar to the outer plaque of the desmosome. In transient expression experiments in COS cells, the recruitment of DP-NTP to cell borders by the chimera required co-expression of plakoglobin. Plakoglobin and DP-NTP co-immunoprecipitated when extracted from L-cells, and yeast two hybrid analysis indicated that DP-NTP binds directly to plakoglobin but not Dsg1. These results identify a role for desmoplakin in organizing the desmosomal cadherin-plakoglobin complex and provide new insights into the hierarchy of protein interactions that occur in the desmosomal plaque.

摘要

桥粒是一种高度组织化的质膜结构域,在细胞间黏附区域将中间丝与质膜连接起来。桥粒包含两类钙黏蛋白,即桥粒芯糖蛋白和桥粒胶蛋白,它们与细胞质蛋白桥粒斑珠蛋白结合。桥粒斑蛋白是桥粒的一个组成部分,在将中间丝网络与桥粒斑连接中起关键作用,桥粒斑蛋白的氨基末端结构域将桥粒斑蛋白靶向到桥粒。然而,尚未鉴定出与桥粒斑蛋白氨基末端结构域结合的桥粒蛋白。为了确定桥粒钙黏蛋白和桥粒斑珠蛋白是否与桥粒斑蛋白的氨基末端结构域相互作用,将这些蛋白在L细胞成纤维细胞中共表达,L细胞是通常不表达桥粒成分的细胞。当在L细胞中表达时,桥粒钙黏蛋白和桥粒斑珠蛋白呈现弥散分布。然而,在存在氨基末端桥粒斑蛋白多肽(DP-NTP)的情况下,观察到桥粒钙黏蛋白和桥粒斑珠蛋白存在于也包含DP-NTP的点状簇中。此外,在共表达具有E-钙黏蛋白细胞外结构域和桥粒芯糖蛋白-1细胞质结构域的嵌合钙黏蛋白的L细胞中,桥粒斑珠蛋白和DP-NTP被募集到细胞-细胞界面,并且这些细胞形成了在超微结构上类似于桥粒外斑的结构。在COS细胞的瞬时表达实验中,嵌合体将DP-NTP募集到细胞边界需要桥粒斑珠蛋白的共表达。当从L细胞中提取时,桥粒斑珠蛋白和DP-NTP共同免疫沉淀,酵母双杂交分析表明DP-NTP直接与桥粒斑珠蛋白结合,而不与桥粒芯糖蛋白1结合。这些结果确定了桥粒斑蛋白在组织桥粒钙黏蛋白-桥粒斑珠蛋白复合物中的作用,并为桥粒斑中发生的蛋白质相互作用层次提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4db2/2141713/37cc5ee88376/JCB.16423f1.jpg

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