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The TIP30 Protein Complex, Arachidonic Acid and Coenzyme A Are Required for Vesicle Membrane Fusion

机译:囊泡膜融合需要TIP30蛋白复合物,花生四烯酸和辅酶A

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摘要

Efficient membrane fusion has been successfully mimicked in vitro using artificial membranes and a number of cellular proteins that are currently known to participate in membrane fusion. However, these proteins are not sufficient to promote efficient fusion between biological membranes, indicating that critical fusogenic factors remain unidentified. We have recently identified a TIP30 protein complex containing TIP30, acyl-CoA synthetase long-chain family member 4 (ACSL4) and Endophilin B1 (Endo B1) that promotes the fusion of endocytic vesicles with Rab5a vesicles, which transport endosomal acidification enzymes vacuolar (H+)-ATPases (V-ATPases) to the early endosomes in vivo. Here, we demonstrate that the TIP30 protein complex facilitates the fusion of endocytic vesicles with Rab5a vesicles in vitro. Fusion of the two vesicles also depends on arachidonic acid, coenzyme A and the synthesis of arachidonyl-CoA by ACSL4. Moreover, the TIP30 complex is able to transfer arachidonyl groups onto phosphatidic acid (PA), producing a new lipid species that is capable of inducing close contact between membranes. Together, our data suggest that the TIP30 complex facilitates biological membrane fusion through modification of PA on membranes.
机译:使用人工膜和目前已知参与膜融合的许多细胞蛋白已成功地在体外模拟了有效的膜融合。然而,这些蛋白质不足以促进生物膜之间的有效融合,这表明关键的融合因子仍未被发现。我们最近发现了一种TIP30蛋白复合物,该复合物包含TIP30,酰基辅酶A合成酶长链家族成员4(ACSL4)和内啡肽B1(Endo B1),可促进内吞囊泡与Rab5a囊泡的融合,后者可转运内体酸化酶液泡(H + )-ATPases(V-ATPases)体内的早期内体。在这里,我们证明了TIP30蛋白复合物可促进Rab5a囊泡在体外与内吞囊泡融合。两个囊泡的融合还取决于花生四烯酸,辅酶A和由ACSL4合成花生四烯酸-辅酶A。此外,TIP30复合物能够将花生四烯基基团转移到磷脂酸(PA)上,从而产生一种新的脂质种类,该种类的脂质能够诱导膜之间的紧密接触。总之,我们的数据表明TIP30复合物通过修饰膜上的PA促进生物膜融合。

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