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CMP
Credit: Jack Hobhouse

Robert Ishmukhametov

Postdoctoral Research Assistant

Sub department

  • Condensed Matter Physics

Research groups

  • Oxford Molecular Motors
Robert.Ishmukhametov@physics.ox.ac.uk
Clarendon Laboratory, room 071,Old Stores,207,273
  • About
  • Publications

A modular platform for one-step assembly of multi-component membrane systems by fusion of charged proteoliposomes

Nature Communications Nature Publishing Group 7 (2016) 13025

Authors:

Robert Ishmukhametov, Aidan N Russell, Richard M Berry

Abstract:

An important goal in synthetic biology is the assembly of biomimetic cell-like structures, which combine multiple biological components in synthetic lipid vesicles. A key limiting assembly step is the incorporation of membrane proteins into the lipid bilayer of the vesicles. Here we present a simple method for delivery of membrane proteins into a lipid bilayer within 5 min. Fusogenic proteoliposomes, containing charged lipids and membrane proteins, fuse with oppositely charged bilayers, with no requirement for detergent or fusion-promoting proteins, and deliver large, fragile membrane protein complexes into the target bilayers. We demonstrate the feasibility of our method by assembling a minimal electron transport chain capable of adenosine triphosphate (ATP) synthesis, combining Escherichia coli F1Fo ATP-synthase and the primary proton pump bo3-oxidase, into synthetic lipid vesicles with sizes ranging from 100 nm to ∼10 μm. This provides a platform for the combination of multiple sets of membrane protein complexes into cell-like artificial structures.
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A simple low-cost device enables four epi-illumination techniques on standard light microscopes

Scientific Reports Nature Publishing Group 6 (2016) 20729

Authors:

Robert Ishmukhametov, Aidan N Russell, Richard J Wheeler, Ashley L Nord, Richard M Berry

Abstract:

Back-scattering darkfield (BSDF), epi-fluorescence (EF), interference reflection contrast (IRC), and darkfield surface reflection (DFSR) are advanced but expensive light microscopy techniques with limited availability. Here we show a simple optical design that combines these four techniques in a simple low-cost miniature epi-illuminator, which inserts into the differential interference-contrast (DIC) slider bay of a commercial microscope, without further additions required. We demonstrate with this device: 1) BSDF-based detection of Malarial parasites inside unstained human erythrocytes; 2) EF imaging with and without dichroic components, including detection of DAPI-stained Leishmania parasite without using excitation or emission filters; 3) RIC of black lipid membranes and other thin films, and 4) DFSR of patterned opaque and transparent surfaces. We believe that our design can expand the functionality of commercial bright field microscopes, provide easy field detection of parasites and be of interest to many users of light microscopy.
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Anatomy of F1-ATPase powered rotation

Proceedings of the National Academy of Sciences (2014)

Authors:

JL Martin, R Ishmukhametov, T Hornung, Z Ahmad, WD Frasch
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ATPase: Overview

Chapter in Encyclopedia of Biophysics, Springer Nature (2013) 134-135
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Interactions between subunits a and b in the rotary ATP synthase as determined by cross-linking

FEBS Letters (2013)

Authors:

J DeLeon-Rangel, RR Ishmukhametov, W Jiang, RH Fillingame, SB Vik
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