Detergent-free Ultrafast Reconstitution of Membrane Proteins into Lipid Bilayers Using Fusogenic Complementary-charged Proteoliposomes.

Journal of visualized experiments : JoVE (2018)

Authors:

Mikhail A Galkin, Aidan N Russell, Steven B Vik, Richard M Berry, Robert R Ishmukhametov

Abstract:

Detergents are indispensable for delivery of membrane proteins into 30-100 nm small unilamellar vesicles, while more complex, larger model lipid bilayers are less compatible with detergents. Here we describe a strategy for bypassing this fundamental limitation using fusogenic oppositely charged liposomes bearing a membrane protein of interest. Fusion between such vesicles occurs within 5 min in a low ionic strength buffer. Positively charged fusogenic liposomes can be used as simple shuttle vectors for detergent-free delivery of membrane proteins into biomimetic target lipid bilayers, which are negatively charged. We also show how to reconstitute membrane proteins into fusogenic proteoliposomes with a fast 30-min protocol. Combining these two approaches, we demonstrate a fast assembly of an electron transport chain consisting of two membrane proteins from E. coli, a primary proton pump bo3-oxidase and F1Fo ATP synthase, in membranes of vesicles of various sizes, ranging from 0.1 to >10 microns, as well as ATP production by this chain.

Degeneracy of gravitational waveforms in the context of GW150914

Journal of Cosmology and Astroparticle Physics IOP Publishing 2018:03 (2018) 007-007

Authors:

James Creswell, Hao Liu, Andrew D Jackson, Sebastian von Hausegger, Pavel Naselsky

A catch-bond drives stator mechanosensitivity in the bacterial flagellar motor

Biophysical Journal Biophysical Society 114:3 S1 (2018)

Authors:

Ashley L Nord, Emilie Gachon, Ruben Perez-Carrasco, Jasmine Nirody, Alessandro Barducci, Richard M Berry, Francesco Pedaci

A blind search for a common signal in gravitational wave detectors

Journal of Cosmology and Astroparticle Physics IOP Publishing 2018:02 (2018) 013-013

Authors:

Hao Liu, James Creswell, Sebastian von Hausegger, Andrew D Jackson, Pavel Naselsky

Imaging of Single Dye-Labeled Chemotaxis Proteins in Live Bacteria Using Electroporation.

Methods in molecular biology (Clifton, N.J.) 1729 (2018) 233-246

Authors:

D Di Paolo, RM Berry

Abstract:

For the last 2 decades, the use of genetically fused fluorescent proteins (FPs) has greatly contributed to the study of chemotactic signaling in E. coli, including the activation of the response regulator protein CheY and its interaction with the flagellar motor. However, this approach suffers from a number of limitations, both biological and biophysical. For example, not all fusions are fully functional when fused to a bulky FP, which can have a similar molecular weight to its fused counterpart. FPs may interfere with the native interactions of the protein, and their chromophores have low brightness and photostability, and fast photobleaching rates. Electroporation allows for internalization of purified CheY proteins labeled with organic dyes into E. coli cells in controllable concentrations. Using fluorescence video microscopy, it is possible to observe single CheY molecules diffusing within cells and interacting with the sensory clusters and the flagellar motors in real time.