-
Je něco špatně v tomto záznamu ?
Treatment of Surface Plasmon Resonance (SPR) Background in Total Internal Reflection Ellipsometry: Characterization of RNA Polymerase II Film Formation
D. Hemzal, YR. Kang, J. Dvořák, T. Kabzinski, K. Kubíček, YD. Kim, J. Humlíček,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články
PubMed
30784293
DOI
10.1177/0003702819826280
Knihovny.cz E-zdroje
- MeSH
- povrchová plasmonová rezonance metody MeSH
- proteinové domény MeSH
- RNA-polymerasa II chemie MeSH
- Saccharomyces cerevisiae - proteiny chemie MeSH
- transkripční faktory chemie MeSH
- vazba proteinů MeSH
- vazebná místa MeSH
- Publikační typ
- časopisecké články MeSH
To deal with the general problem of biomolecule specific binding analysis, we have applied the technique of difference spectra to the surface plasmon resonance (SPR)-enhanced total internal reflection ellipsometry measurement. We suggest a three-step treatment of the SPR background that can easily be integrated with the usual measurement routine. First, making use of the difference spectrum in ellipsometric angle Δ, single peak footprints of the topmost layer are obtained that facilitate its sensitive detection during film growth. Subsequently, circumventing the need for explicit knowledge of the substrate properties, the difference spectra peaks can be used for the end-point analysis of a binding. Finally, tracking the binding effectivity of the analyte we determine the injection speed and analyte concentration windows needed for successful monitoring of the film growth. We demonstrate our approach on a comprehensive two-stage binding experiment involving two biologically relevant molecules: the C-terminal domain (CTD) of RNA polymerase II and CTD-interacting domain of one of its transcription factors, the Rtt103 protein.
CEITEC Central European Institute of Technology Masaryk University Brno Czech Republic
Department of Condensed Matter Physics Masaryk University Brno Czech Republic
Department of Physics Kyung Hee University Seoul Republic of Korea
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc19034763
- 003
- CZ-PrNML
- 005
- 20191010110259.0
- 007
- ta
- 008
- 191007s2019 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1177/0003702819826280 $2 doi
- 035 __
- $a (PubMed)30784293
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Hemzal, Dušan $u 1 Department of Condensed Matter Physics, Masaryk University, Brno, Czech Republic. 2 CEITEC - Central European Institute of Technology, Masaryk University, Brno, Czech Republic.
- 245 10
- $a Treatment of Surface Plasmon Resonance (SPR) Background in Total Internal Reflection Ellipsometry: Characterization of RNA Polymerase II Film Formation / $c D. Hemzal, YR. Kang, J. Dvořák, T. Kabzinski, K. Kubíček, YD. Kim, J. Humlíček,
- 520 9_
- $a To deal with the general problem of biomolecule specific binding analysis, we have applied the technique of difference spectra to the surface plasmon resonance (SPR)-enhanced total internal reflection ellipsometry measurement. We suggest a three-step treatment of the SPR background that can easily be integrated with the usual measurement routine. First, making use of the difference spectrum in ellipsometric angle Δ, single peak footprints of the topmost layer are obtained that facilitate its sensitive detection during film growth. Subsequently, circumventing the need for explicit knowledge of the substrate properties, the difference spectra peaks can be used for the end-point analysis of a binding. Finally, tracking the binding effectivity of the analyte we determine the injection speed and analyte concentration windows needed for successful monitoring of the film growth. We demonstrate our approach on a comprehensive two-stage binding experiment involving two biologically relevant molecules: the C-terminal domain (CTD) of RNA polymerase II and CTD-interacting domain of one of its transcription factors, the Rtt103 protein.
- 650 _2
- $a vazebná místa $7 D001665
- 650 _2
- $a vazba proteinů $7 D011485
- 650 _2
- $a proteinové domény $7 D000072417
- 650 _2
- $a RNA-polymerasa II $x chemie $7 D012319
- 650 _2
- $a Saccharomyces cerevisiae - proteiny $x chemie $7 D029701
- 650 _2
- $a povrchová plasmonová rezonance $x metody $7 D020349
- 650 _2
- $a transkripční faktory $x chemie $7 D014157
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Kang, Yu Ri $u 3 Department of Physics, Kyung Hee University, Seoul, Republic of Korea.
- 700 1_
- $a Dvořák, Jan $u 1 Department of Condensed Matter Physics, Masaryk University, Brno, Czech Republic.
- 700 1_
- $a Kabzinski, Tomasz $u 2 CEITEC - Central European Institute of Technology, Masaryk University, Brno, Czech Republic.
- 700 1_
- $a Kubíček, Karel $u 2 CEITEC - Central European Institute of Technology, Masaryk University, Brno, Czech Republic.
- 700 1_
- $a Kim, Young Dong $u 3 Department of Physics, Kyung Hee University, Seoul, Republic of Korea.
- 700 1_
- $a Humlíček, Josef $u 1 Department of Condensed Matter Physics, Masaryk University, Brno, Czech Republic. 2 CEITEC - Central European Institute of Technology, Masaryk University, Brno, Czech Republic.
- 773 0_
- $w MED00008276 $t Applied spectroscopy $x 1943-3530 $g Roč. 73, č. 3 (2019), s. 261-270
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/30784293 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20191007 $b ABA008
- 991 __
- $a 20191010110718 $b ABA008
- 999 __
- $a ok $b bmc $g 1451423 $s 1073313
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 73 $c 3 $d 261-270 $e 20190220 $i 1943-3530 $m Applied spectroscopy $n Appl Spectrosc $x MED00008276
- LZP __
- $a Pubmed-20191007