|
|
|
|
LEADER |
01000naa a22002652 4500 |
001 |
NLM222451920 |
003 |
DE-627 |
005 |
20231224054315.0 |
007 |
cr uuu---uuuuu |
008 |
231224s2012 xx |||||o 00| ||eng c |
024 |
7 |
|
|a 10.1021/la303987c
|2 doi
|
028 |
5 |
2 |
|a pubmed24n0741.xml
|
035 |
|
|
|a (DE-627)NLM222451920
|
035 |
|
|
|a (NLM)23134267
|
040 |
|
|
|a DE-627
|b ger
|c DE-627
|e rakwb
|
041 |
|
|
|a eng
|
100 |
1 |
|
|a González-Campo, Arántzazu
|e verfasserin
|4 aut
|
245 |
1 |
0 |
|a Supramolecularly oriented immobilization of proteins using cucurbit[8]uril
|
264 |
|
1 |
|c 2012
|
336 |
|
|
|a Text
|b txt
|2 rdacontent
|
337 |
|
|
|a ƒaComputermedien
|b c
|2 rdamedia
|
338 |
|
|
|a ƒa Online-Ressource
|b cr
|2 rdacarrier
|
500 |
|
|
|a Date Completed 23.07.2013
|
500 |
|
|
|a Date Revised 25.11.2016
|
500 |
|
|
|a published: Print-Electronic
|
500 |
|
|
|a Citation Status MEDLINE
|
520 |
|
|
|a A supramolecular strategy is used for oriented positioning of proteins on surfaces. A viologen-based guest molecule is attached to the surface, while a naphthol guest moiety is chemoselectively ligated to a yellow fluorescent protein. Cucurbit[8]uril (CB[8]) is used to link the proteins onto surfaces through specific charge-transfer interactions between naphthol and viologen inside the CB cavity. The assembly process is characterized using fluorescence and atomic force microscopy, surface plasmon resonance, IR-reflective absorption, and X-ray photoelectron spectroscopy measurements. Two different immobilization routes are followed to form patterns of the protein ternary complexes on the surfaces. Each immobilization route consists of three steps: (i) attaching the viologen to the glass using microcontact chemistry, (ii) blocking, and (iii) either incubation or microcontact printing of CB[8] and naphthol guests. In both cases uniform and stable fluorescent patterns are fabricated with a high signal-to-noise ratio. Control experiments confirm that CB[8] serves as a selective linking unit to form stable and homogeneous ternary surface-bound complexes as envisioned. The attachment of the yellow fluorescent protein complexes is shown to be reversible and reusable for assembly as studied using fluorescence microscopy
|
650 |
|
4 |
|a Journal Article
|
650 |
|
4 |
|a Research Support, Non-U.S. Gov't
|
650 |
|
7 |
|a Bridged-Ring Compounds
|2 NLM
|
650 |
|
7 |
|a Imidazoles
|2 NLM
|
650 |
|
7 |
|a Immobilized Proteins
|2 NLM
|
650 |
|
7 |
|a Luminescent Proteins
|2 NLM
|
650 |
|
7 |
|a Naphthols
|2 NLM
|
650 |
|
7 |
|a Quaternary Ammonium Compounds
|2 NLM
|
650 |
|
7 |
|a cucurbit(8)uril
|2 NLM
|
700 |
1 |
|
|a Brasch, Melanie
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Uhlenheuer, Dana A
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Gómez-Casado, Alberto
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Yang, Lanti
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Brunsveld, Luc
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Huskens, Jurriaan
|e verfasserin
|4 aut
|
700 |
1 |
|
|a Jonkheijm, Pascal
|e verfasserin
|4 aut
|
773 |
0 |
8 |
|i Enthalten in
|t Langmuir : the ACS journal of surfaces and colloids
|d 1992
|g 28(2012), 47 vom: 27. Nov., Seite 16364-71
|w (DE-627)NLM098181009
|x 1520-5827
|7 nnns
|
773 |
1 |
8 |
|g volume:28
|g year:2012
|g number:47
|g day:27
|g month:11
|g pages:16364-71
|
856 |
4 |
0 |
|u http://dx.doi.org/10.1021/la303987c
|3 Volltext
|
912 |
|
|
|a GBV_USEFLAG_A
|
912 |
|
|
|a SYSFLAG_A
|
912 |
|
|
|a GBV_NLM
|
912 |
|
|
|a GBV_ILN_22
|
912 |
|
|
|a GBV_ILN_350
|
912 |
|
|
|a GBV_ILN_721
|
951 |
|
|
|a AR
|
952 |
|
|
|d 28
|j 2012
|e 47
|b 27
|c 11
|h 16364-71
|