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The ins and outs of membrane bending by intrinsically disordered proteins.
Yuan, Feng; Lee, Christopher T; Sangani, Arjun; Houser, Justin R; Wang, Liping; Lafer, Eileen M; Rangamani, Padmini; Stachowiak, Jeanne C.
Affiliation
  • Yuan F; Department of Biomedical Engineering, The University of Texas at Austin, Austin, TX, USA.
  • Lee CT; Department of Mechanical and Aerospace Engineering, University of California San Diego, La Jolla, CA, USA.
  • Sangani A; Department of Biomedical Engineering, The University of Texas at Austin, Austin, TX, USA.
  • Houser JR; Department of Biomedical Engineering, The University of Texas at Austin, Austin, TX, USA.
  • Wang L; Department of Biochemistry and Structural Biology, The University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
  • Lafer EM; Department of Biochemistry and Structural Biology, The University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
  • Rangamani P; Department of Mechanical and Aerospace Engineering, University of California San Diego, La Jolla, CA, USA.
  • Stachowiak JC; Department of Biomedical Engineering, The University of Texas at Austin, Austin, TX, USA.
Sci Adv ; 9(27): eadg3485, 2023 07 07.
Article in En | MEDLINE | ID: mdl-37418523
ABSTRACT
Membrane curvature is essential to diverse cellular functions. While classically attributed to structured domains, recent work illustrates that intrinsically disordered proteins are also potent drivers of membrane bending. Specifically, repulsive interactions among disordered domains drive convex bending, while attractive interactions drive concave bending, creating membrane-bound, liquid-like condensates. How might disordered domains that contain both repulsive and attractive domains affect curvature? Here, we examined chimeras that combined attractive and repulsive interactions. When the attractive domain was closer to the membrane, its condensation amplified steric pressure among repulsive domains, leading to convex curvature. In contrast, when the repulsive domain was closer to the membrane, attractive interactions dominated, resulting in concave curvature. Further, a transition from convex to concave curvature occurred with increasing ionic strength, which reduced repulsion while enhancing condensation. In agreement with a simple mechanical model, these results illustrate a set of design rules for membrane bending by disordered proteins.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Intrinsically Disordered Proteins / Membranes Language: En Journal: Sci Adv Year: 2023 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Intrinsically Disordered Proteins / Membranes Language: En Journal: Sci Adv Year: 2023 Document type: Article Affiliation country: Estados Unidos