Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1791
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dc.contributor.authorRakshit, S.-
dc.date.accessioned2020-11-18T09:13:17Z-
dc.date.available2020-11-18T09:13:17Z-
dc.date.issued2017-
dc.identifier.citationAnalytical Biochemistry, 535en_US
dc.identifier.other10.1016/j.ab.2017.07.022-
dc.identifier.urihttps://pubmed.ncbi.nlm.nih.gov/28756135/-
dc.identifier.urihttp://hdl.handle.net/123456789/1791-
dc.description.abstractWe have developed a method for Enzymatic Sortase-assisted Covalent Orientation-specific Restraint Tethering (ESCORT) recombinant proteins onto surfaces directly from cell-lysate. With an improved surface passivation method, we obviate the cumbersome purification steps even for single molecule studies that demand high purity in the sample. We demonstrated high-specificity of the method, high-passivity of the surface and uncompromised functional integrity of anchored proteins using single molecule fluorescence and force-mapping. We anticipate that this method will substantially reduce the investment by way of time, money and energy in the area of single molecule studies.en_US
dc.language.isoen_USen_US
dc.publisherPubmed.en_US
dc.subjectProtein-protein interactionsen_US
dc.subjectPull-down assaysen_US
dc.subjectSurface modificationen_US
dc.titleESCORTing proteins directly from whole cell-lysate for single-molecule studiesen_US
dc.typeArticleen_US
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