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231224s2012 xx |||||o 00| ||eng c |
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|a 10.1021/la204524w
|2 doi
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|a pubmed25n0715.xml
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|e rakwb
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|a eng
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| 100 |
1 |
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|a Glassford, Stefanie
|e verfasserin
|4 aut
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| 245 |
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|a Chemical imaging of protein adsorption and crystallization on a wettability gradient surface
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|c 2012
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|a Text
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|2 rdacontent
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|a ƒaComputermedien
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|2 rdamedia
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|a ƒa Online-Ressource
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|2 rdacarrier
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|a Date Completed 08.06.2012
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|a Date Revised 14.02.2012
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a The use of self-assembled monolayers is an established method to study the effect of surface properties on proteins and other biological materials. The generation of a monolayer with a gradient of chemical properties allows for the study of multiple surface properties simultaneously in a high throughput manner. Typically, in order to detect the presence of proteins or biological material on a surface, the use of additional dyes or tags is required. Here we present a novel method of studying the effect of gradient surface properties on protein adsorption and crystallization in situ through the use of ATR-FTIR spectroscopic imaging, which removes the need for additional labeling. We describe the successful application of this technique to the measurement of the growth of a gradient monolayer of octyltrichlorosilane across the surface of a silicon ATR element. ATR-FTIR imaging was also used to study the adsorption of lysozyme, as a model protein, onto the modified surface. The sensitivity of measurements obtained with a focal plane array (FPA) detector were improved though the use of pixel averaging which allowed small absorption bands to be detected with minimal effect on the spatial resolution along the gradient. Study of the effect of surface hydrophobicity on both adsorption of lysozyme to the element and lysozyme crystallization revealed that more lysozyme adsorbed to the hydrophobic side of the ATR element and more lysozyme crystals formed in the same region. These findings strongly suggest a correlation exists between surface protein adsorption and protein crystallization. This method could be applied to the study of other proteins and whole cells
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|a Journal Article
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|a Research Support, Non-U.S. Gov't
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|a Proteins
|2 NLM
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| 700 |
1 |
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|a Chan, K L Andrew
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Byrne, Bernadette
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Kazarian, Sergei G
|e verfasserin
|4 aut
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| 773 |
0 |
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|i Enthalten in
|t Langmuir : the ACS journal of surfaces and colloids
|d 1985
|g 28(2012), 6 vom: 14. Feb., Seite 3174-9
|w (DE-627)NLM098181009
|x 1520-5827
|7 nnns
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| 773 |
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|g volume:28
|g year:2012
|g number:6
|g day:14
|g month:02
|g pages:3174-9
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|u http://dx.doi.org/10.1021/la204524w
|3 Volltext
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