Formation of cytoplasmic turns between two closely spaced transmembrane helices during membrane protein integration into the ER membrane

被引:9
作者
Sääf, A [1 ]
Hermansson, M [1 ]
von Heijne, G [1 ]
机构
[1] Univ Stockholm, Dept Biochem, S-10691 Stockholm, Sweden
关键词
membrane protein; topology; glycosylation; transmembrane helix;
D O I
10.1006/jmbi.2000.3933
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
The helical hairpin, two closely spaced transmembrane helices separated by a short turn, is a recurring structural element in integral membrane proteins, and may serve as a compact unit that inserts into the membrane En bloc. Previously, we have determined the propensities of the 20 natural amino acids, when present in the middle of a long hydrophobic stretch, to induce the formation of a helical hairpin with a lumenally exposed turn during membrane protein assembly into the endoplasmic reticulum membrane. Here, we present results from a similar set of measurements, but with the turn placed on the cytoplasmic side of the membrane. We find that a significantly higher number of turn-promoting residues need to be present to induce a cytoplasmic turn compared to a lumenal turn, and that, in contrast to the lumenal turn, the positively charged residues Arg and Lys are the strongest turn-promoters in cytoplasmic turns. These results suggest that the process of turn formation between transmembrane helices is different for lumenal and cytoplasmic turns. (C) 2000 Academic Press.
引用
收藏
页码:191 / 197
页数:7
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