| Literature DB >> 29938845 |
Jordyn Atwater1,2, Daniela S Mattes3,4, Bettina Streit3, Clemens von Bojničić-Kninski3, Felix F Loeffler3, Frank Breitling3, Harald Fuchs1,5, Michael Hirtz1.
Abstract
Surface-bound microarrays of multiple oligo- and macromolecules (e.g., peptides, DNA) offer versatile options in biomedical applications like drug screening, DNA analysis, or medical diagnostics. Combinatorial syntheses of these molecules in situ can save significant resources in regard to processing time and material use. Furthermore, high feature densities are needed to enable high-throughput and low sample volumes as generally regarded in combinatorial chemistry. Here, a scanning-probe-lithography-based approach for the combinatorial in situ synthesis of macromolecules is presented in microarray format. Feature sizes below 40 µm allow for the creation of high-density arrays with feature densities of 62 500 features per cm2 . To demonstrate feasibility of this approach for biomedical applications, a multiplexed array of functional protein tags (HA- and FLAG-tag) is synthesized, and selective binding of respective epitope recognizing antibodies is shown. This approach uses only small amounts of base chemicals for synthesis and can be further parallelized, therefore, opening up a route to flexible, highly dense, and cost-effective microarrays.Entities:
Keywords: combinatorial chemistry; high-throughput screening; microarrays; peptides; scanning probe lithography
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Year: 2018 PMID: 29938845 DOI: 10.1002/adma.201801632
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849