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通过酵母展示鉴定拟南芥纤维素合酶亚基 3 的稳定片段。

Identifying Stable Fragments of Arabidopsis thaliana Cellulose Synthase Subunit 3 by Yeast Display.

机构信息

Department of Chemical and Biomolecular Engineering, University of Tennessee at Knoxville, Knoxville, TN 37996.

Center for Structural Molecular Biology and Neutron Scsattering Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831.

出版信息

Biotechnol J. 2019 Apr;14(4):e1800353. doi: 10.1002/biot.201800353. Epub 2018 Sep 25.

Abstract

Determining structures of large, complex proteins remains challenging, especially for transmembrane proteins, as the protein size increases. Arabidopsis thaliana cellulose synthesis complex is a large, multimeric complex located in the plant cell membrane that synthesizes cellulose microfibrils in the plant cell wall. Despite the biological and economic importance of cellulose and therefore cellulose synthesis, many aspects of the cellulase synthase complex (CSC) structure and function are still unknown. Here, yeast surface display (YSD) is used to determine the full-length expression of A. thaliana cellulose synthase 3 (AtCesA3) fragments. The level of stably-folded AtCesA3 fragments displayed on the yeast surface are determined using flow cytometric analysis of differential surface expression of epitopes flanking the AtCesA3 fragment. This technique provides a fast and simple method for examining folding and expression of protein domains and fragments of complex proteins.

摘要

确定大型复杂蛋白质的结构仍然具有挑战性,特别是对于跨膜蛋白,因为随着蛋白质大小的增加。拟南芥纤维素合成复合物是一种位于植物细胞膜中的大型多聚体复合物,在植物细胞壁中合成纤维素微纤维。尽管纤维素及其合成在生物学和经济上都很重要,但纤维素合酶复合物(CSC)的许多结构和功能方面仍然未知。在这里,酵母表面展示(YSD)用于确定全长表达的拟南芥纤维素合酶 3(AtCesA3)片段。通过对侧翼 AtCesA3 片段的表位进行流式细胞术分析,确定稳定折叠的 AtCesA3 片段在酵母表面的表达水平。该技术为检查复杂蛋白质的结构域和片段的折叠和表达提供了一种快速简单的方法。

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