<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Cookis T</submitter><funding>NIGMS NIH HHS</funding><pubmed_abstract>Streptavidin affinity grids provide strategies to overcome many commonly encountered cryo-electron microscopy (cryo-EM) sample preparation challenges, including sample denaturation and preferential orientations that can occur due to the air-water interface. Streptavidin affinity grids, however, are currently utilized by few cryo-EM labs because they are not commercially available and require a careful fabrication process. Two-dimensional streptavidin crystals are grown onto a biotinylated lipid monolayer that is applied directly to standard holey-carbon cryo-EM grids. The high-affinity interaction between streptavidin and biotin allows for the subsequent binding of biotinylated samples that are protected from the air-water interface during cryo-EM sample preparation. Additionally, these grids provide a strategy for concentrating samples available in limited quantities and purifying protein complexes of interest directly on the grids. Here, a step-by-step, optimized protocol is provided for the robust fabrication of streptavidin affinity grids for use in cryo-EM and negative-stain experiments. Additionally, a trouble-shooting guide is included for commonly experienced challenges to make the use of streptavidin affinity grids more accessible to the larger cryo-EM community.</pubmed_abstract><journal>Journal of visualized experiments : JoVE</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11293040</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Streptavidin-Affinity Grid Fabrication for Cryo-Electron Microscopy Sample Preparation.</pubmed_title><pmcid>PMC11293040</pmcid><funding_grant_id>R35 GM127018</funding_grant_id><pubmed_authors>Nogales E</pubmed_authors><pubmed_authors>Han BG</pubmed_authors><pubmed_authors>Cookis T</pubmed_authors><pubmed_authors>Glaeser R</pubmed_authors><pubmed_authors>Poepsel S</pubmed_authors><pubmed_authors>Herbst DA</pubmed_authors><pubmed_authors>Sauer P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Streptavidin-Affinity Grid Fabrication for Cryo-Electron Microscopy Sample Preparation.</name><description>Streptavidin affinity grids provide strategies to overcome many commonly encountered cryo-electron microscopy (cryo-EM) sample preparation challenges, including sample denaturation and preferential orientations that can occur due to the air-water interface. Streptavidin affinity grids, however, are currently utilized by few cryo-EM labs because they are not commercially available and require a careful fabrication process. Two-dimensional streptavidin crystals are grown onto a biotinylated lipid monolayer that is applied directly to standard holey-carbon cryo-EM grids. The high-affinity interaction between streptavidin and biotin allows for the subsequent binding of biotinylated samples that are protected from the air-water interface during cryo-EM sample preparation. Additionally, these grids provide a strategy for concentrating samples available in limited quantities and purifying protein complexes of interest directly on the grids. Here, a step-by-step, optimized protocol is provided for the robust fabrication of streptavidin affinity grids for use in cryo-EM and negative-stain experiments. Additionally, a trouble-shooting guide is included for commonly experienced challenges to make the use of streptavidin affinity grids more accessible to the larger cryo-EM community.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Dec</publication><modification>2025-04-19T20:45:18.223Z</modification><creation>2025-02-19T02:27:09.114Z</creation></dates><accession>S-EPMC11293040</accession><cross_references><pubmed>38224121</pubmed><doi>10.3791/66197</doi></cross_references></HashMap>