HEGER, Zbynek, Natalia CERNEI, Sona KRIZKOVA, Michal MASAŘÍK, Pavel KOPEL, Petr HODEK, Ondrej ZITKA, Vojtech ADAM and Rene KIZEK. Paramagnetic Nanoparticles as a Platform for FRET-Based Sarcosine Picomolar Detection. Scientific Reports. London: Nature Publishing Group, 2015, vol. 5, "8868", p. 1-7. ISSN 2045-2322. Available from: https://dx.doi.org/10.1038/srep08868.
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Basic information
Original name Paramagnetic Nanoparticles as a Platform for FRET-Based Sarcosine Picomolar Detection
Authors HEGER, Zbynek (203 Czech Republic), Natalia CERNEI (203 Czech Republic), Sona KRIZKOVA (203 Czech Republic), Michal MASAŘÍK (203 Czech Republic, guarantor, belonging to the institution), Pavel KOPEL (203 Czech Republic), Petr HODEK (203 Czech Republic), Ondrej ZITKA (203 Czech Republic), Vojtech ADAM (203 Czech Republic) and Rene KIZEK (203 Czech Republic).
Edition Scientific Reports, London, Nature Publishing Group, 2015, 2045-2322.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30105 Physiology
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 5.228
RIV identification code RIV/00216224:14110/15:00083933
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1038/srep08868
UT WoS 000350549200018
Keywords in English Prostate-cancer progression; Urine samples; Diagnostics; Carcinoma
Tags EL OK
Tags International impact, Reviewed
Changed by Changed by: Soňa Böhmová, učo 232884. Changed: 22/9/2015 14:38.
Abstract
Herein, we describe an ultrasensitive specific biosensing system for detection of sarcosine as a potential biomarker of prostate carcinoma based on Forster resonance energy transfer (FRET). The FRET biosensor employs anti-sarcosine antibodies immobilized on paramagnetic nanoparticles surface for specific antigen binding. Successful binding of sarcosine leads to assembly of a sandwich construct composed of anti-sarcosine antibodies keeping the Forster distance (Ro) of FRET pair in required proximity. The detection is based on spectral overlap between gold-functionalized green fluorescent protein and antibodies@quantum dots bioconjugate (lambda(ex) 400 nm). The saturation curve of sarcosine based on FRET efficiency (F-604/F-510 ratio) was tested within linear dynamic range from 5 to 50 nM with detection limit down to 50 pM. Assembled biosensor was then successfully employed for sarcosine quantification in prostatic cell lines (PC3, 22Rv1, PNT1A), and urinary samples of prostate adenocarcinoma patients.
Links
ED1.1.00/02.0068, research and development projectName: CEITEC - central european institute of technology
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