Mechanically Enhancing Planar Lipid Bilayers with a Minimal Actin Cortex

被引:7
作者
Burden, Daniel L. [1 ]
Kim, Daniel [1 ]
Cheng, Wayland [1 ]
Lawler, Emily Chandler [1 ]
Burden, Lisa M. Keranen [2 ]
机构
[1] Wheaton Coll, Dept Chem, Wheaton, IL 60187 USA
[2] Wheaton Coll, Dept Biol, Wheaton, IL 60187 USA
基金
美国国家科学基金会;
关键词
F-ACTIN; NANOPORE; RECONSTITUTION; MEMBRANES; CHANNELS; STABILIZATION; FABRICATION; PROTEINS; DYNAMICS; SENSORS;
D O I
10.1021/acs.langmuir.8b01847
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
All cells in all domains of life possess a cytoskeleton that provides mechanical resistance to deformation and general stability to the plasma membrane. Here, we utilize a two-dimensional scaffolding created by actin filaments to convey mechanical support upon relatively fragile planar bilayer membranes (black lipid membranes, BLMs). Robust biomembranes play a critical role in the development of protein nanopore sensor applications and might also prove helpful in ion-channel research. Our investigation utilizes a minimal actin cortex (MAC) that is formed by anchoring actin filaments to lipid membranes via a biotin streptavidin biotin bridge. We characterize the joined structure using various modes of optical microscopy, electrophysiology, and applied mechanical stress (including measurements of elastic modulus). Our findings show the resulting structure includes a thin supporting layer of actin. Electrical studies indicate that the integrity of the MAC bilayer composite remains unchanged over the limits of our tests (i.e., hours to days). The actin filament structure can remain intact for months. Minimalistic layering of the actin support network produces an increase in the apparent elastic modulus of the MAC-derivatized bilayer by >100x, compared to unmodified BLMs. Furthermore, the resistance to applied stress improves with the number of actin layers, which can be cross-linked to arbitrary thicknesses, in principle. The weblike support structure retains the lateral fluidity of the BLM, maintains the high electrical resistance typical of traditional BLMs, enables relatively uninhibited molecular access to the lipid surface from bulk solution, and permits nanopore self-assembly and insertion in the bilayer. These interfacial features are highly desirable for ion-channel and nanopore sensing applications.
引用
收藏
页码:10847 / 10855
页数:9
相关论文
共 54 条
  • [1] Alberts B, 2015, MOL BIOL CELL
  • [2] Tethered and Polymer Supported Bilayer Lipid Membranes: Structure and Function
    Andersson, Jakob
    Koper, Ingo
    [J]. MEMBRANES, 2016, 6 (02):
  • [3] Photolithographic Fabrication of Microapertures with Well-Defined, Three-Dimensional Geometries for Suspended Lipid Membrane Studies
    Baker, Christopher A.
    Bright, Leonard K.
    Aspinwall, Craig A.
    [J]. ANALYTICAL CHEMISTRY, 2013, 85 (19) : 9078 - 9086
  • [4] Methacrylate Polymer Scaffolding Enhances the Stability of Suspended Lipid Bilayers for Ion Channel Recordings and Biosensor Development
    Bright, Leonard K.
    Baker, Christopher A.
    Branstrom, Robert
    Saavedra, S. Scott
    Aspinwall, Craig A.
    [J]. ACS BIOMATERIALS SCIENCE & ENGINEERING, 2015, 1 (10): : 955 - 963
  • [5] Decreased Aperture Surface Energy Enhances Electrical, Mechanical, and Temporal Stability of Suspended Lipid Membranes
    Bright, Leonard K.
    Baker, Christopher A.
    Agasid, Mark T.
    Ma, Lin
    Aspinwall, Craig A.
    [J]. ACS APPLIED MATERIALS & INTERFACES, 2013, 5 (22) : 11918 - 11926
  • [6] Diffusion bias and photophysical dynamics of single molecules in unsupported lipid bilayer membranes probed with confocal microscopy
    Burden, DL
    Kasianowicz, JJ
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (26) : 6103 - 6107
  • [7] Membrane surface dynamics of DNA-threaded nanopores revealed by simultaneous single-molecule optical and ensemble electrical recording
    Chandler, EL
    Smith, AL
    Burden, LM
    Kasianowicz, JJ
    Burden, DL
    [J]. LANGMUIR, 2004, 20 (03) : 898 - 905
  • [8] Selective Detection of Protein Homologues in Serum Using an OmpG Nanopore
    Fahie, Monifa A.
    Yang, Bib
    Mullis, Martin
    Holden, Matthew A.
    Chen, Min
    [J]. ANALYTICAL CHEMISTRY, 2015, 87 (21) : 11143 - 11149
  • [9] Rapid metagenomic identification of viral pathogens in clinical samples by real-time nanopore sequencing analysis
    Greninger, Alexander L.
    Naccache, Samia N.
    Federman, Scot
    Yu, Guixia
    Mbala, Placide
    Bres, Vanessa
    Stryke, Doug
    Bouquet, Jerome
    Somasekar, Sneha
    Linnen, Jeffrey M.
    Dodd, Roger
    Mulembakani, Prime
    Schneider, Bradley S.
    Muyembe-Tamfum, Jean-Jacques
    Stramer, Susan L.
    Chiu, Charles Y.
    [J]. GENOME MEDICINE, 2015, 7
  • [10] Gu Li-Qun, 2013, Methods Mol Biol, V1024, P255, DOI 10.1007/978-1-62703-453-1_21