Wilde A, Dempsey C, Banting G
Department of Biochemistry, School of Medical Sciences, University of Bristol, United Kingdom.
J Biol Chem. 1994 Mar 11;269(10):7131-6.
TGN38 and TGN41 are isoforms of an integral membrane protein (TGN38/41) which is predominantly located in the trans-Golgi network of mammalian cells, but which constitutively recycles between the TGN and the plasma membrane. The cytoplasmic domain tetrapeptide sequence "YQRL" is responsible for the internalization of TGN38/41 from the plasma membrane. This sequence conforms to the tyrosine containing internalization motif ("YXXhydro," where X is any amino acid and hydro is any large bulky hydrophobic amino acid) found in other integral membrane proteins which are internalized from the plasma membrane via clathrin-coated vesicles. Structural predictions have suggested that the YXXhydro motif might adopt a tight turn structure in solution, a prediction supported previously by nuclear magnetic resonance (NMR) studies on short synthetic peptides corresponding to variants of the generic YXXhydro motif. We have synthesized a 21-amino acid peptide which encompasses the TGN38/41 internalization motif and used it as template for two-dimensional NMR analysis. The data from these experiments demonstrate that the internalization motif in the cytoplasmic domain of TGN38/41 lies within a nascent helix, not a tight turn. This is the first study to show that tyrosine containing internalization motifs do not necessarily adopt a beta-turn conformation.
TGN38和TGN41是一种整合膜蛋白(TGN38/41)的亚型,该蛋白主要位于哺乳动物细胞的反式高尔基体网络中,但会在反式高尔基体网络和质膜之间持续循环。胞质结构域四肽序列“YQRL”负责TGN38/41从质膜的内化。该序列符合在其他通过网格蛋白包被小泡从质膜内化的整合膜蛋白中发现的含酪氨酸内化基序(“YXXhydro”,其中X是任何氨基酸,hydro是任何大的疏水性氨基酸)。结构预测表明,YXXhydro基序在溶液中可能采用紧密转角结构,这一预测先前得到了对与通用YXXhydro基序变体相对应的短合成肽的核磁共振(NMR)研究的支持。我们合成了一种包含TGN38/41内化基序的21个氨基酸的肽,并将其用作二维NMR分析的模板。这些实验的数据表明,TGN38/41胞质结构域中的内化基序位于新生螺旋内,而非紧密转角内。这是第一项表明含酪氨酸内化基序不一定采用β转角构象的研究。