Search: WFRF:(Anderson Eugene) > (2007-2009) > A global benchmark ...
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000 | 08021naa a2202089 4500 | |
001 | oai:DiVA.org:sh-13911 | |
003 | SwePub | |
008 | 111214s2009 | |||||||||||000 ||eng| | |
024 | 7 | a https://urn.kb.se/resolve?urn=urn:nbn:se:sh:diva-139112 URI |
024 | 7 | a https://doi.org/10.1016/j.ab.2008.11.0212 DOI |
040 | a (SwePub)sh | |
041 | a engb eng | |
042 | 9 SwePub | |
072 | 7 | a ref2 swepub-contenttype |
072 | 7 | a art2 swepub-publicationtype |
100 | 1 | a Rich, Rebecca L.4 aut |
245 | 1 0 | a A global benchmark study using affinity-based biosensors |
264 | 1 | b Elsevier BV,c 2009 |
338 | a print2 rdacarrier | |
520 | a To explore the variability in biosensor studies, 150 participants from 20 countries were given the same protein samples and asked to determine kinetic rate constants for the interaction. We chose a protein system that was amenable to analysis using different biosensor platforms as well as by users of different expertise levels. The two proteins (a 50-kDa Fab and a 60-kDa glutathione S-transferase [GST] antigen) form a relatively high-affinity complex, so participants needed to optimize several experimental parameters, including ligand immobilization and regeneration conditions as well as analyte concentrations and injection/dissociation times. Although most participants collected binding responses that could be fit to yield kinetic parameters, the quality of a few data sets could have been improved by optimizing the assay design. Once these outliers were removed, the average reported affinity across the remaining panel of participants was 620 pM with a standard deviation of 980 pM. These results demonstrate that when this biosensor assay was designed and executed appropriately, the reported rate constants were consistent, and independent of which protein was immobilized and which biosensor was used. | |
650 | 7 | a NATURVETENSKAPx Biologix Biokemi och molekylärbiologi0 (SwePub)106022 hsv//swe |
650 | 7 | a NATURAL SCIENCESx Biological Sciencesx Biochemistry and Molecular Biology0 (SwePub)106022 hsv//eng |
700 | 1 | a Papalia, Giuseppe A.4 aut |
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700 | 1 | a Clabbers, Anca4 aut |
700 | 1 | a Wieckowski, Sebastien4 aut |
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700 | 1 | a Page, Phillip4 aut |
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700 | 1 | a Laird-Offringa, Ite4 aut |
700 | 1 | a Lee, Charlene S.4 aut |
700 | 1 | a Khadir, Abdelkrim4 aut |
700 | 1 | a Podlaski, Frank4 aut |
700 | 1 | a Neuner, Phillippe4 aut |
700 | 1 | a Rothacker, Julie4 aut |
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700 | 1 | a Dankbar, Nico4 aut |
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700 | 1 | a Ly, Nguyen4 aut |
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710 | 2 | a Södertörns högskolab Molekylärbiologi4 org |
773 | 0 | t Analytical Biochemistryd : Elsevier BVg 386:2, s. 194-216q 386:2<194-216x 0003-2697x 1096-0309 |
856 | 4 | u https://europepmc.org/articles/pmc3793259?pdf=render |
856 | 4 8 | u https://urn.kb.se/resolve?urn=urn:nbn:se:sh:diva-13911 |
856 | 4 8 | u https://doi.org/10.1016/j.ab.2008.11.021 |
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