TY - JOUR
T1 - The ins and outs of membrane bending by intrinsically disordered proteins
AU - Yuan, Feng
AU - Lee, Christopher T.
AU - Sangani, Arjun
AU - Houser, Justin R.
AU - Wang, Liping
AU - Lafer, Eileen M.
AU - Rangamani, Padmini
AU - Stachowiak, Jeanne C.
N1 - Publisher Copyright:
© 2023 The Authors.
PY - 2023/7/7
Y1 - 2023/7/7
N2 - 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.
AB - 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.
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U2 - 10.1126/sciadv.adg3485
DO - 10.1126/sciadv.adg3485
M3 - Article
C2 - 37418523
AN - SCOPUS:85164267194
SN - 2375-2548
VL - 9
SP - eadg3485
JO - Science Advances
JF - Science Advances
IS - 27
M1 - adg3485
ER -