The ins and outs of membrane bending by intrinsically disordered proteins

被引:15
|
作者
Yuan, Feng [1 ]
Lee, Christopher T. [2 ]
Sangani, Arjun [1 ]
Houser, Justin R. [1 ]
Wang, Liping [3 ]
Lafer, Eileen M. [3 ]
Rangamani, Padmini [2 ]
Stachowiak, Jeanne C. [1 ,4 ]
机构
[1] Univ Texas Austin, Dept Biomed Engn, Austin, TX 78712 USA
[2] Univ Calif San Diego, Dept Mech & Aerosp Engn, La Jolla, CA 92093 USA
[3] Univ Texas Hlth Sci Ctr San Antonio, Dept Biochem & Struct Biol, San Antonio, TX USA
[4] Univ Texas Austin, Dept Chem Engn, Austin, TX 78712 USA
关键词
NUCLEAR-PORE COMPLEX; PHASE-SEPARATION; CURVATURE; TRANSPORT; BRUSHES; POLYMER; DOMAIN;
D O I
10.1126/sciadv.adg3485
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页数:12
相关论文
共 50 条
  • [41] Intrinsically disordered proteins and multicellular organisms
    Dunker, A. Keith
    Bondos, Sarah E.
    Huang, Fei
    Oldfield, Christopher J.
    SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2015, 37 : 44 - 55
  • [42] Classification of Intrinsically Disordered Regions and Proteins
    van der Lee, Robin
    Buljan, Marija
    Lang, Benjamin
    Weatheritt, Robert J.
    Daughdrill, Gary W.
    Dunker, A. Keith
    Fuxreiter, Monika
    Gough, Julian
    Gsponer, Joerg
    Jones, David T.
    Kim, Philip M.
    Kriwacki, Richard W.
    Oldfield, Christopher J.
    Pappu, Rohit V.
    Tompa, Peter
    Uversky, Vladimir N.
    Wright, Peter E.
    Babu, M. Madan
    CHEMICAL REVIEWS, 2014, 114 (13) : 6589 - 6631
  • [43] Fine structures of intrinsically disordered proteins
    Seth, Swarnadeep
    Stine, Brandon
    Bhattacharya, Aniket
    JOURNAL OF CHEMICAL PHYSICS, 2024, 160 (01):
  • [44] Intrinsically disordered proteins from A to Z
    Uversky, Vladimir N.
    INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2011, 43 (08): : 1090 - 1103
  • [45] The binding mechanisms of intrinsically disordered proteins
    Dogan, Jakob
    Gianni, Stefano
    Jemth, Per
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2014, 16 (14) : 6323 - 6331
  • [46] Intrinsically disordered proteins in human mitochondria
    Ito, Masahiro
    Tohsato, Yukako
    Sugisawa, Hitoshi
    Kohara, Shohei
    Fukuchi, Satoshi
    Nishikawa, Ikuko
    Nishikawa, Ken
    GENES TO CELLS, 2012, 17 (10) : 817 - 825
  • [47] Proline Fingerprint in Intrinsically Disordered Proteins
    Murrali, Maria Grazia
    Piai, Alessandro
    Bermel, Wolfgang
    Felli, Isabella C.
    Pierattelli, Roberta
    CHEMBIOCHEM, 2018, 19 (15) : 1625 - 1629
  • [48] Allosteric Modulation of Intrinsically Disordered Proteins
    Rehman, Ashfaq Ur
    Rahman, Mueed Ur
    Arshad, Taaha
    Chen, Hai-Feng
    PROTEIN ALLOSTERY IN DRUG DISCOVERY, 2019, 1163 : 335 - 357
  • [49] MobiDB: intrinsically disordered proteins in 2021
    Piovesan, Damiano
    Necci, Marco
    Escobedo, Nahuel
    Monzon, Alexander Miguel
    Hatos, Andras
    Micetic, Ivan
    Quaglia, Federica
    Paladin, Lisanna
    Ramasamy, Pathmanaban
    Dosztanyi, Zsuzsanna
    Vranken, Wim F.
    Davey, Norman E.
    Parisi, Gustavo
    Fuxreiter, Monika
    Tosatto, Silvio C. E.
    NUCLEIC ACIDS RESEARCH, 2021, 49 (D1) : D361 - D367
  • [50] Intrinsically disordered regions in autophagy proteins
    Mei, Yang
    Su, Minfei
    Soni, Gaurav
    Salem, Saeed
    Colbert, Christopher L.
    Sinha, Sangita C.
    PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 2014, 82 (04) : 565 - 578