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来自酿酒酵母的内质网-囊泡蛋白Erv41p腔结构域的纯化、结晶及初步X射线晶体学分析。

Purification, crystallization and preliminary X-ray crystallographic analysis of the lumenal domain of the ER-vesicle protein Erv41p from Saccharomyces cerevisiae.

作者信息

Biterova Ekaterina I, Svärd Maria, Possner Dominik D D, Guy Jodie E

机构信息

Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Tomtebodavägen 6, S171-77 Stockholm, Sweden.

出版信息

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2013 May 1;69(Pt 5):544-6. doi: 10.1107/S1744309113008063. Epub 2013 Apr 30.

DOI:10.1107/S1744309113008063
PMID:23695573
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3660897/
Abstract

The membrane protein Erv41p is a major component of COPII-coated vesicles and is thought to play a role in the early secretory pathway in eukaryotic cells. In this study, the full lumenal domain of Erv41p from Saccharomyces cerevisiae (ScErv41p_LD) was recombinantly expressed in Sf9 insect cells and purified by nickel-affinity, ion-exchange and size-exclusion chromatography. ScErv41p_LD crystals were obtained using the sitting-drop vapour-diffusion method and native X-ray diffraction data were collected to 2.0 Å resolution. The crystals belonged to space group P21, with unit-cell parameters a = 49.8, b = 76.9, c = 65.1 Å, α = γ = 90.0, β = 104.8°.

摘要

膜蛋白Erv41p是COPII被膜小泡的主要成分,被认为在真核细胞的早期分泌途径中发挥作用。在本研究中,酿酒酵母的Erv41p的完整腔结构域(ScErv41p_LD)在Sf9昆虫细胞中重组表达,并通过镍亲和、离子交换和尺寸排阻色谱法进行纯化。使用坐滴气相扩散法获得了ScErv41p_LD晶体,并收集了分辨率为2.0 Å的天然X射线衍射数据。晶体属于空间群P21,晶胞参数为a = 49.8、b = 76.9、c = 65.1 Å,α = γ = 90.0,β = 104.8°。

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The Erv41p-Erv46p complex: multiple export signals are required in trans for COPII-dependent transport from the ER.Erv41p-Erv46p复合物:从内质网进行COPII依赖的转运需要多个反式输出信号。
EMBO J. 2002 Nov 15;21(22):6095-104. doi: 10.1093/emboj/cdf598.
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Erv41p and Erv46p: new components of COPII vesicles involved in transport between the ER and Golgi complex.Erv41p和Erv46p:参与内质网与高尔基体复合体之间转运的COPII囊泡新组分。
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