Molecular imprinting technology for targeted analysis of proteins
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216305%3A26620%2F17%3APU128358" target="_blank" >RIV/00216305:26620/17:PU128358 - isvavai.cz</a>
Alternative codes found
RIV/62156489:43210/17:43912625
Result on the web
<a href="https://mendelnet.cz/artkey/mnt-201701-0098_Molecular-imprinting-technology-for-targeted-analysis-of-proteins.php?back=/magno/mnt/2017/mn1.php?secid=4" target="_blank" >https://mendelnet.cz/artkey/mnt-201701-0098_Molecular-imprinting-technology-for-targeted-analysis-of-proteins.php?back=/magno/mnt/2017/mn1.php?secid=4</a>
DOI - Digital Object Identifier
—
Alternative languages
Result language
angličtina
Original language name
Molecular imprinting technology for targeted analysis of proteins
Original language description
Molecular imprinting has appeared to be an effective technique for creating of selective recognition sites in synthetic polymers. This procedure comprises polymerization of monomer in a presence of target molecules (template). The subsequent template removal forms tailor-made cavities that are complementary in shape and size to the template molecules. For protein imprinting, the choice of the suitable polymers is limited and polymerization conditions need to be optimized. In our work, dopamine monomer was chosen for polymer formation due to its nontoxicity, ease of preparation and self-assembly. For the optimization of conditions, lysozyme with molecular weight 14.3 kDa was used and the functionality was evaluated by fluorimetry. Different concentration of dopamine and lysozyme for polymerization were tested. Under the optimized conditions, the limit of detection for lysozyme was found to be 7.8 µg/ml. Moreover, conditions for polymer formation for a purpose to reduce the overall time of analysis were investigated. The use of dopamine as a monomer in molecular imprinting shown to be beneficial in many aspects.
Czech name
—
Czech description
—
Classification
Type
D - Article in proceedings
CEP classification
—
OECD FORD branch
10608 - Biochemistry and molecular biology
Result continuities
Project
<a href="/en/project/LQ1601" target="_blank" >LQ1601: CEITEC 2020</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2017
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Article name in the collection
MendelNet 2017
ISBN
978-80-7509-529-9
ISSN
—
e-ISSN
—
Number of pages
5
Pages from-to
873-877
Publisher name
Mendel University in Brno
Place of publication
Neuveden
Event location
Brno
Event date
Nov 8, 2017
Type of event by nationality
CST - Celostátní akce
UT code for WoS article
000440194500156