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<p>Membrane proteins inhabit a uniquely heterogeneous environment in which folding, insertion, and assembly are inseparably coupled to the physical properties of lipid bilayers. Despite their central biological relevance, the principles governing membrane protein folding are less well defined than those for soluble proteins due to the energetic complexity of transferring polypeptide chains across, into, or along membranes. This review examines the biophysical determinants that shape the early stages of α-helical membrane protein folding, emphasizing the membrane-water interface as a critical energetic gateway. We trace the historical development of hydrophobic scales, from early solvent-based peptide measurements to membrane-translocon-derived scales, highlighting how successive refinement has revealed distinct energetic preferences for aqueous, interfacial, and fully inserted states. Building on this framework, we discuss how co-translational folding within the ribosome exit tunnel and the ribosome-translocon complex constrains secondary structure formation and modulates the final behavior of the polypeptide segment. We further analyze the contributions of intrahelical and interhelical interactions, lipid-protein coupling, and bilayer adaptability in stabilizing transmembrane helices and promoting higher-order assembly. Finally, we integrate these concepts into a unified view in which membrane protein biogenesis emerges as a continuous energy-driven process where sequence-encoded information, molecular machinery, and membrane physics converge to ensure faithful folding, topogenesis, and quality control.</p>

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Living at the border: biophysical gateways into membrane protein insertion and folding

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年2月4日

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  • Brayan Grau,
  • Ismael Mingarro

摘要

Membrane proteins inhabit a uniquely heterogeneous environment in which folding, insertion, and assembly are inseparably coupled to the physical properties of lipid bilayers. Despite their central biological relevance, the principles governing membrane protein folding are less well defined than those for soluble proteins due to the energetic complexity of transferring polypeptide chains across, into, or along membranes. This review examines the biophysical determinants that shape the early stages of α-helical membrane protein folding, emphasizing the membrane-water interface as a critical energetic gateway. We trace the historical development of hydrophobic scales, from early solvent-based peptide measurements to membrane-translocon-derived scales, highlighting how successive refinement has revealed distinct energetic preferences for aqueous, interfacial, and fully inserted states. Building on this framework, we discuss how co-translational folding within the ribosome exit tunnel and the ribosome-translocon complex constrains secondary structure formation and modulates the final behavior of the polypeptide segment. We further analyze the contributions of intrahelical and interhelical interactions, lipid-protein coupling, and bilayer adaptability in stabilizing transmembrane helices and promoting higher-order assembly. Finally, we integrate these concepts into a unified view in which membrane protein biogenesis emerges as a continuous energy-driven process where sequence-encoded information, molecular machinery, and membrane physics converge to ensure faithful folding, topogenesis, and quality control.