High S, Flint N, Dobberstein B
European Molecular Biology Laboratory, Heidelberg, Germany.
J Cell Biol. 1991 Apr;113(1):25-34. doi: 10.1083/jcb.113.1.25.
Proteins which are inserted and anchored in the membrane of the ER by an uncleaved signal-anchor sequence can assume two final orientations. Type I signal-anchor proteins translocate the NH2 terminus across the membrane while type II signal-anchor proteins translocate the COOH terminus. We investigated the requirements for cytosolic protein components and nucleotides for the membrane targeting and insertion of single-spanning type I signal-anchor proteins. Besides the ribosome, signal recognition particle (SRP), GTP, and rough microsomes (RMs) no other components were found to be required. The GTP analogue GMPPNP could substitute for GTP in supporting the membrane insertion of IMC-CAT. By using a photocrosslinking assay we show that for secreted, type I and type II signal-anchor proteins the presence of both GTP and RMs is required for the release of the nascent chain from the 54-kD subunit of SRP. For two of the proteins studied the release of the nascent chain from SRP54 was accompanied by a new interaction with components of the ER. We conclude that the GTP-dependent release of the nascent chain from SRP54 occurs in an identical manner for each of the proteins studied.
通过未切割的信号锚定序列插入并锚定在内质网(ER)膜中的蛋白质可以呈现两种最终取向。I型信号锚定蛋白将NH2末端转运穿过膜,而II型信号锚定蛋白则转运COOH末端。我们研究了单跨膜I型信号锚定蛋白靶向膜并插入膜所需的胞质蛋白成分和核苷酸。除了核糖体、信号识别颗粒(SRP)、GTP和糙面微粒体(RMs)外,未发现其他成分是必需的。GTP类似物GMPPNP可以替代GTP来支持IMC-CAT的膜插入。通过使用光交联分析,我们表明,对于分泌型、I型和II型信号锚定蛋白,GTP和RMs的存在都是新生链从SRP的54-kD亚基释放所必需的。对于所研究的两种蛋白质,新生链从SRP54的释放伴随着与内质网成分的新相互作用。我们得出结论,对于所研究的每种蛋白质,新生链从SRP54的GTP依赖性释放以相同的方式发生。