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dc.contributor.authorMenger, Marcus and Yarman, Aysu and Erdossy, Julia and Yildiz, Huseyin Bekir and Gyurcsanyi, Robert E. and Scheller, Frieder W.
dc.date.accessioned2020-08-07T14:18:39Z
dc.date.available2020-08-07T14:18:39Z
dc.date.issued2016
dc.identifier10.3390/bios6030035
dc.identifier.issn2079-6374
dc.identifier.urihttp://hdl.handle.net/20.500.12498/4666
dc.description.abstractBiomimetic 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.
dc.language.isoEnglish
dc.publisherMDPI
dc.sourceBIOSENSORS-BASEL
dc.titleMIPs and Aptamers for Recognition of Proteins in Biomimetic Sensing
dc.typeReview


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