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• W2047243609 abstract "In a current model of integration of multispanning membrane proteins into the endoplasmic reticulum, it is proposed that the transmembrane segments show alternating translocation initiation and stop-transfer functions. Here, we present evidence for a mode of cotranslational insertion in which an internal signal-anchor sequence with Nexo/Ccyt topology confers a transmembrane disposition onto a preceding hydrophilic segment, resulting in a topology where the hydrophilic segment apparently can slip back and forth across the membrane. Our results demonstrate that hydrophobicity is not, as hitherto thought, an absolute requirement for the formation of a transmembrane segment, and suggest that integral membrane proteins may contain hydrophilic transmembrane segments with a considerable freedom to move in relation to the membrane." @default.
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• W2047243609 date "1998-10-01" @default.
• W2047243609 modified "2023-09-27" @default.
• W2047243609 title "Forced Transmembrane Orientation of Hydrophilic Polypeptide Segments in Multispanning Membrane Proteins" @default.
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• W2047243609 doi "https://doi.org/10.1016/s1097-2765(00)80149-5" @default.
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