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在存在GTP受限的arf1突变体的情况下积累的COPI囊泡缺乏顺行和逆行货物。

COPI vesicles accumulating in the presence of a GTP restricted arf1 mutant are depleted of anterograde and retrograde cargo.

作者信息

Pepperkok R, Whitney J A, Gomez M, Kreis T E

机构信息

Cell Biophysics and Cell Biology Program, EMBL Heidelberg, Meyerhofstr.1, Germany.

出版信息

J Cell Sci. 2000 Jan;113 ( Pt 1):135-44. doi: 10.1242/jcs.113.1.135.

Abstract

Microinjection of the slowly hydrolyzable GTP analogue GTP(gamma)S or the ectopic expression of a GTP restricted mutant of the small GTPase arf1 (arf1[Q71L]) leads to the rapid accumulation of COPI coated vesicles and buds in living cells. This effect is blocked at 15 degrees C and by microinjection of antibodies against (beta)-COP. Anterograde and retrograde membrane protein transport markers, which have been previously shown to be incorporated into COPI vesicles between the endoplasmic reticulum and Golgi complex, are depleted from the GTP(gamma)S or arf1[Q71L] induced COPI coated vesicles and buds. In contrast, in control cells 30 to 60% of the COPI carriers co-localize with these markers. These in vivo data corroborate recent in vitro work, suggesting that GTP(gamma)S and arf1[Q71L] interfere with the sorting of membrane proteins into Golgi derived COPI vesicles, and provide the first in vivo evidence for a role of GTP hydrolysis by arf1 in the sorting of cargo into COPI coated vesicles and buds.

摘要

向活细胞中微量注射缓慢水解的GTP类似物GTP(γ)S或小GTP酶arf1的GTP限制突变体(arf1[Q71L])的异位表达会导致COPI包被小泡和芽在活细胞中迅速积累。这种效应在15摄氏度时以及通过微量注射抗β-COP抗体被阻断。先前已证明在内质网和高尔基体复合体之间被整合到COPI小泡中的顺行和逆行膜蛋白转运标记物,在GTP(γ)S或arf1[Q71L]诱导的COPI包被小泡和芽中减少。相比之下,在对照细胞中,30%至60%的COPI载体与这些标记物共定位。这些体内数据证实了最近的体外研究工作,表明GTP(γ)S和arf1[Q71L]干扰膜蛋白分选到高尔基体衍生的COPI小泡中,并为arf1的GTP水解在货物分选到COPI包被小泡和芽中的作用提供了首个体内证据。

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