Positively and negatively charged residues have different effects on the position in the membrane of a model transmembrane helix

被引:92
作者
Monné, M
Nilsson, I
Johansson, M
Elmhed, N
von Heijne, G [1 ]
机构
[1] Univ Stockholm, Dept Biochem, S-10691 Stockholm, Sweden
[2] Karolinska Inst, NOVUM, Dept Biosci, S-14157 Huddinge, Sweden
关键词
membrane protein; protein structure; glycosylation; transmembrane helix; charged residues;
D O I
10.1006/jmbi.1998.2218
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have studied the effects of single charged residues on the position of a model transmembrane helix in the endoplasmic reticulum membrane using the glycosylation mapping technique. Asp and Glu residues cause a re-positioning of the C-terminal end of the transmembrane helix when placed in the one to two C-terminal turns but not when placed more centrally. Arg and Lys residues, in contrast, have little effect when placed in the two C-terminal turn but give rise to a more substantial shift in position when placed 9-11 residues from the helix end. We suggest that this difference between the effects of positively and negatively charged residues can be explained by the so-called snorkel effect, i.e. that the very long side-chains of Arg and Lys can reach up along the transmembrane helix to allow the terminal, charged moiety to reside in the lipid headgroup region while the C-alpha of the residue is positioned well below the membrane/water interface. (C) 1998 Academic Press.
引用
收藏
页码:1177 / 1183
页数:7
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