Das Suchergebnis hat sich seit Ihrer Suchanfrage verändert. Eventuell werden Dokumente in anderer Reihenfolge angezeigt.
  • Treffer 10 von 30202
Zurück zur Trefferliste

MIPs and aptamers for recognition of proteins in biomimetic sensing

  • Biomimetic binders and catalysts have been generated in order to substitute the biological pendants in separation techniques and bioanalysis. The two major approaches use either "evolution in the test tube" of nucleotides for the preparation of aptamers or total chemical synthesis for molecularly imprinted polymers (MIPs). The reproducible production of aptamers is a clear advantage, whilst the preparation of MIPs typically leads to a population of polymers with different binding sites. The realization of binding sites in the total bulk of the MIPs results in a higher binding capacity, however, on the expense of the accessibility and exchange rate. Furthermore, the readout of the bound analyte is easier for aptamers since the integration of signal generating labels is well established. On the other hand, the overall negative charge of the nucleotides makes aptamers prone to non-specific adsorption of positively charged constituents of the sample and the "biological" degradation of non-modified aptamers and ionic strength-dependentBiomimetic binders and catalysts have been generated in order to substitute the biological pendants in separation techniques and bioanalysis. The two major approaches use either "evolution in the test tube" of nucleotides for the preparation of aptamers or total chemical synthesis for molecularly imprinted polymers (MIPs). The reproducible production of aptamers is a clear advantage, whilst the preparation of MIPs typically leads to a population of polymers with different binding sites. The realization of binding sites in the total bulk of the MIPs results in a higher binding capacity, however, on the expense of the accessibility and exchange rate. Furthermore, the readout of the bound analyte is easier for aptamers since the integration of signal generating labels is well established. On the other hand, the overall negative charge of the nucleotides makes aptamers prone to non-specific adsorption of positively charged constituents of the sample and the "biological" degradation of non-modified aptamers and ionic strength-dependent changes of conformation may be challenging in some application.zeige mehrzeige weniger

Volltext Dateien herunterladen

  • pmnr357.pdfeng
    (2021KB)

    SHA-1:f0c5e405a463a868518e29dfc2c6e920207b476d

Metadaten exportieren

Weitere Dienste

Suche bei Google Scholar Statistik - Anzahl der Zugriffe auf das Dokument
Metadaten
Verfasserangaben:Marcus Menger, Aysu YarmanORCiDGND, Júlia Erdőssy, Huseyin Bekir Yildiz, Róbert E. Gyurcsányi, Frieder W. SchellerORCiDGND
URN:urn:nbn:de:kobv:517-opus4-400496
Schriftenreihe (Bandnummer):Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe (357)
Publikationstyp:Postprint
Sprache:Englisch
Datum der Erstveröffentlichung:22.09.2017
Erscheinungsjahr:2017
Veröffentlichende Institution:Universität Potsdam
Datum der Freischaltung:22.09.2017
Freies Schlagwort / Tag:SELEX; aptamers; aptasensors; biomimetic recognition elements; chemical sensors; in vitro selection; molecularly imprinted polymers
Seitenanzahl:19
Quelle:Biosensors 6 (2016) Nr. 3. - DOI: 10.3390/bios6030035
Organisationseinheiten:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Biochemie und Biologie
DDC-Klassifikation:5 Naturwissenschaften und Mathematik / 57 Biowissenschaften; Biologie / 570 Biowissenschaften; Biologie
Peer Review:Referiert
Publikationsweg:Open Access
Fördermittelquelle:Multidisciplinary Digital Publishing Institute (MDPI)
Lizenz (Deutsch):License LogoCC-BY - Namensnennung 4.0 International
Verstanden ✔
Diese Webseite verwendet technisch erforderliche Session-Cookies. Durch die weitere Nutzung der Webseite stimmen Sie diesem zu. Unsere Datenschutzerklärung finden Sie hier.