On-grid purification of electron microscopy samples via a 3D-printed flow-cell

While recent advances in cryogenic electron microscopy coupled with single particle analysis have the potential to allow structure determination in a near-native state from vanishingly few individual particles, this vision has yet to be realised in practise. Requirements for particle numbers that currently far exceed the theoretical lower limits, challenges with the practicalities of achieving such concentrations for difficult-to-produce samples, and inadequate sample-dependent imaging conditions, all result in significant bottlenecks preventing routine structure determination using cryo-EM. Therefore, considerable efforts are being made to circumvent these bottlenecks by developing affinity purification of samples on-grid; at once obviating the need to produce large amounts of protein, as well as more directly controlling the variable, and sample-dependent, process of grid preparation. In this proof-of-concept study, we demonstrate a further practical step towards this paradigm, developing a 3D-printable flow-cell device to allow on-grid affinity purification from raw inputs such as whole cell lysates, using graphene oxide-based affinity grids. Our flow-cell device can be interfaced directly with routinely-used laboratory equipment such as liquid chromatographs, or peristaltic pumps, fitted with standard chromatographic (1/16”) connectors, and can be used to allow binding of samples to affinity grids in a controlled environment prior to extensive washing to remove impurities. Furthermore, by designing a device which can be 3D printed and coupled to routinely used laboratory equipment, we hope to increase the accessibility of the techniques presented herein to researchers working towards single-particle protein structures.

[1]  J. Heddle,et al.  Programmable polymorphism of a virus-like particle , 2021, Communications Materials.

[2]  Christopher H. S. Aylett,et al.  Preparation of Sample Support Films in Transmission Electron Microscopy using a Support Floatation Block , 2021, Journal of visualized experiments : JoVE.

[3]  Christopher H. S. Aylett,et al.  Direct transfer of electron microscopy samples to wetted carbon and graphene films via a support floatation block , 2020, Journal of structural biology.

[4]  Mitchell H. Murdock,et al.  mGreenLantern: a bright monomeric fluorescent protein with rapid expression and cell filling properties for neuronal imaging , 2020, Proceedings of the National Academy of Sciences.

[5]  D. Agard,et al.  General and robust covalently linked graphene oxide affinity grids for high-resolution cryo-EM , 2019, Proceedings of the National Academy of Sciences.

[6]  M. Howarth,et al.  Approaching infinite affinity through engineering of peptide–protein interaction , 2019, Proceedings of the National Academy of Sciences.

[7]  Christopher H. S. Aylett,et al.  Bacteriophage MS2 displays unreported capsid variability assembling T = 4 and mixed capsids , 2019, Molecular microbiology.

[8]  F. Dimaio,et al.  3.1Å structure of yeast RNA polymerase II elongation complex stalled at a cyclobutane pyrimidine dimer lesion solved using streptavidin affinity grids , 2019, bioRxiv.

[9]  Yong Zi Tan,et al.  Reducing effects of particle adsorption to the air–water interface in cryo-EM , 2018, Nature Methods.

[10]  Martin Grininger,et al.  The deadly touch: protein denaturation at the water-air interface and how to prevent it , 2018, bioRxiv.

[11]  T. Shintake,et al.  Improved sample dispersion in cryo-EM using "perpetually-hydrated" graphene oxide flakes. , 2018, Journal of structural biology.

[12]  Henning Stahlberg,et al.  Miniaturizing EM Sample Preparation: Opportunities, Challenges, and “Visual Proteomics” , 2018, Proteomics.

[13]  R. Glaeser PROTEINS, INTERFACES, AND CRYO-EM GRIDS. , 2017, Current opinion in colloid & interface science.

[14]  Jamie H. D. Cate,et al.  Monolayer-Crystal Streptavidin Support Films Provide an Internal Standard of cryo-EM Image Quality , 2016, bioRxiv.

[15]  Wen Jiang,et al.  Antibody-Based Affinity Cryo-Electron Microscopy at 2.6 Å Resolution , 2016, bioRxiv.

[16]  Wen Jiang,et al.  Selective Capture of Histidine-tagged Proteins from Cell Lysates Using TEM grids Modified with NTA-Graphene Oxide , 2016, Scientific Reports.

[17]  Robert M Glaeser,et al.  Long shelf-life streptavidin support-films suitable for electron microscopy of biological macromolecules. , 2016, Journal of structural biology.

[18]  Wen Jiang,et al.  Antibody-based affinity cryo-EM grid. , 2016, Methods.

[19]  N. Ranson,et al.  An introduction to sample preparation and imaging by cryo-electron microscopy for structural biology , 2016, Methods.

[20]  Dominika Elmlund,et al.  Cryogenic electron microscopy and single-particle analysis. , 2015, Annual review of biochemistry.

[21]  Wen Jiang,et al.  Single-step antibody-based affinity cryo-electron microscopy for imaging and structural analysis of macromolecular assemblies. , 2014, Journal of structural biology.

[22]  Lori A. Passmore,et al.  Controlling protein adsorption on graphene for cryo-EM using low-energy hydrogen plasmas , 2014, Nature Methods.

[23]  M. Llaguno,et al.  Chemically functionalized carbon films for single molecule imaging. , 2014, Journal of structural biology.

[24]  Ana Sofia Pina,et al.  Challenges and opportunities in the purification of recombinant tagged proteins , 2013, Biotechnology Advances.

[25]  Deborah F. Kelly,et al.  Capturing Enveloped Viruses on Affinity Grids for Downstream Cryo-Electron Microscopy Applications , 2013, Microscopy and Microanalysis.

[26]  P. Arbeláez,et al.  Electron microscopy of biotinylated protein complexes bound to streptavidin monolayer crystals. , 2012, Journal of structural biology.

[27]  Johannes E. Schindelin,et al.  Fiji: an open-source platform for biological-image analysis , 2012, Nature Methods.

[28]  B. Zakeri,et al.  Peptide tag forming a rapid covalent bond to a protein, through engineering a bacterial adhesin , 2012, Proceedings of the National Academy of Sciences.

[29]  Andreas Hierlemann,et al.  Connecting μ-fluidics to electron microscopy. , 2012, Journal of structural biology.

[30]  Carl W. Magnuson,et al.  Graphene: Substrate preparation and introduction. , 2011, Journal of structural biology.

[31]  Thomas Walz,et al.  Strategy for the use of affinity grids to prepare non-His-tagged macromolecular complexes for single-particle electron microscopy. , 2010, Journal of molecular biology.

[32]  Wolfgang Baumeister,et al.  Graphene oxide: a substrate for optimizing preparations of frozen-hydrated samples. , 2010, Journal of structural biology.

[33]  Liguo Wang,et al.  Streptavidin crystals as nanostructured supports and image-calibration references for cryo-EM data collection. , 2008, Journal of structural biology.

[34]  Priyanka D Abeyrathne,et al.  The Affinity Grid: a pre-fabricated EM grid for monolayer purification. , 2008, Journal of molecular biology.

[35]  Deborah F. Kelly,et al.  Monolayer purification: A rapid method for isolating protein complexes for single-particle electron microscopy , 2008, Proceedings of the National Academy of Sciences.

[36]  Wen Jiang,et al.  EMAN2: an extensible image processing suite for electron microscopy. , 2007, Journal of structural biology.

[37]  D. Waugh,et al.  Making the most of affinity tags. , 2005, Trends in biotechnology.

[38]  Patrick Schultz,et al.  Immobilization of biotinylated DNA on 2-D streptavidin crystals. , 2004, Journal of structural biology.

[39]  R. Henderson The potential and limitations of neutrons, electrons and X-rays for atomic resolution microscopy of unstained biological molecules , 1995, Quarterly Reviews of Biophysics.

[40]  R. Kornberg,et al.  Two-dimensional crystals of streptavidin on biotinylated lipid layers and their interactions with biotinylated macromolecules. , 1991, Biophysical journal.