-
Something wrong with this record ?
Peptide Functionalization of Gold Nanoparticles for the Detection of Carcinoembryonic Antigen in Blood Plasma via SPR-Based Biosensor
ML. Ermini, X. Chadtová Song, T. Špringer, J. Homola
Language English Country Switzerland
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
NV16-27611A
MZ0
CEP Register
Digital library NLK
Full text - Article
NLK
Directory of Open Access Journals
from 2013
PubMed Central
from 2013
Europe PubMed Central
from 2013
Open Access Digital Library
from 2013-01-01
Open Access Digital Library
from 2013-01-01
ROAD: Directory of Open Access Scholarly Resources
from 2013
- MeSH
- Hematologic Tests methods MeSH
- Carcinoembryonic Antigen * blood MeSH
- Plasma chemistry MeSH
- Humans MeSH
- Biomarkers, Tumor analysis MeSH
- Nanoparticles analysis MeSH
- Peptides analysis MeSH
- Surface Plasmon Resonance methods MeSH
- Gold analysis MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Nanoparticles functionalized with specific biological recognition molecules play a major role for sensor response enhancement in surface plasmon resonance (SPR) based biosensors. The functionalization procedure of such nanoparticles is crucial, since it influences their interactions with the environment and determines their applicability to biomolecular detection in complex matrices. In this work we show how the ζ-potential (Zpot) of bio-functionalized gold spherical NPs (Bio-NPs) is related to the SPR sensor response enhancement of an immune-sandwich-assay for the detection of the carcinoembryonic antigen (CEA), a cancer marker for colorectal carcinomas. In particular, we prepare bio-functional nanoparticles by varying the amount of peptide (either streptavidin or antibody against CEA) bound on their surface. Specific and non-specific sensor responses, reproducibility, and colloidal stability of those bio-functional nanoparticles are measured via SPR and compared to ζ-potential values. Those parameters are first measured in buffer solution, then measured again when the surface of the biosensor is exposed to blood plasma, and finally when the nanoparticles are immersed in blood plasma and flowed overnight on the biosensor. We found that ζ-potential values can guide the design of bio-functional NPs with improved binding efficiency and reduced non-specific sensor response, suitable reproducibility and colloidal stability, even in complex matrixes like blood plasma.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc21029267
- 003
- CZ-PrNML
- 005
- 20230118081130.0
- 007
- ta
- 008
- 211203s2019 sz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.3389/fchem.2019.00040 $2 doi
- 035 __
- $a (PubMed)30778384
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sz
- 100 1_
- $a Ermini, Maria Laura $u Institute of Photonics and Electronics, Czech Academy of Sciences, Prague, Czechia
- 245 10
- $a Peptide Functionalization of Gold Nanoparticles for the Detection of Carcinoembryonic Antigen in Blood Plasma via SPR-Based Biosensor / $c ML. Ermini, X. Chadtová Song, T. Špringer, J. Homola
- 520 9_
- $a Nanoparticles functionalized with specific biological recognition molecules play a major role for sensor response enhancement in surface plasmon resonance (SPR) based biosensors. The functionalization procedure of such nanoparticles is crucial, since it influences their interactions with the environment and determines their applicability to biomolecular detection in complex matrices. In this work we show how the ζ-potential (Zpot) of bio-functionalized gold spherical NPs (Bio-NPs) is related to the SPR sensor response enhancement of an immune-sandwich-assay for the detection of the carcinoembryonic antigen (CEA), a cancer marker for colorectal carcinomas. In particular, we prepare bio-functional nanoparticles by varying the amount of peptide (either streptavidin or antibody against CEA) bound on their surface. Specific and non-specific sensor responses, reproducibility, and colloidal stability of those bio-functional nanoparticles are measured via SPR and compared to ζ-potential values. Those parameters are first measured in buffer solution, then measured again when the surface of the biosensor is exposed to blood plasma, and finally when the nanoparticles are immersed in blood plasma and flowed overnight on the biosensor. We found that ζ-potential values can guide the design of bio-functional NPs with improved binding efficiency and reduced non-specific sensor response, suitable reproducibility and colloidal stability, even in complex matrixes like blood plasma.
- 650 _7
- $a peptidy $x analýza $7 D010455 $2 czmesh
- 650 _7
- $a zlato $x analýza $7 D006046 $2 czmesh
- 650 _7
- $a nanočástice $x analýza $7 D053758 $2 czmesh
- 650 _7
- $a krevní plazma $x chemie $7 D010949 $2 czmesh
- 650 _7
- $a povrchová plasmonová rezonance $x metody $7 D020349 $2 czmesh
- 650 17
- $a karcinoembryonální antigen $x krev $7 D002272 $2 czmesh
- 650 _7
- $a hematologické testy $x metody $7 D006403 $2 czmesh
- 650 _7
- $a nádorové biomarkery $x analýza $7 D014408 $2 czmesh
- 650 _7
- $a lidé $7 D006801 $2 czmesh
- 655 _2
- $a časopisecké články $7 D016428
- 655 _7
- $a práce podpořená grantem $7 D013485 $2 czmesh
- 700 1_
- $a Chadtová Song, Xue $u Institute of Photonics and Electronics, Czech Academy of Sciences, Prague, Czechia
- 700 1_
- $a Špringer, Tomáš $u Institute of Photonics and Electronics, Czech Academy of Sciences, Prague, Czechia
- 700 1_
- $a Homola, Jiří $u Institute of Photonics and Electronics, Czech Academy of Sciences, Prague, Czechia
- 773 0_
- $w MED00208456 $t Frontiers in chemistry $x 2296-2646 $g Roč. 7, č. - (2019), s. 40
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/30778384 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20211203 $b ABA008
- 991 __
- $a 20230118081125 $b ABA008
- 999 __
- $a kom $b bmc $g 1730262 $s 1149820
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 7 $c - $d 40 $e 20190204 $i 2296-2646 $m Frontiers in chemistry $n Front Chem $x MED00208456
- GRA __
- $a NV16-27611A $p MZ0
- LZP __
- $c NLK120 $d 20230117 $a 2021-granty