Frank F. Bier
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Frank F. Bier has a total of 8 co-authors. Here are the top co-authors by number of shared publications:
- Alexander Christmann
Fraunhofer Institute of Biomedical Engineering (IBMT), Dpt. Molecular Bioanalytics and Bioelectronics, Arthur-Scheunert-Allee 114-116, 14558 Nuthetal, Germany
1 shared publication - Eva Ehrentreich-Förster
Fraunhofer Institute for Biomedical Technology, Am Mühlenberg 13, Potsdam, 14476, Germany
1 shared publication Frank Kleinjung
Noxxon Pharma AG, Gustav-Meyer-Allee 25, 10234 Berlin, Germany
1 shared publication- Markus von Nickisch-Rosenegk
Fraunhofer Institute of Biomedical Engineering (IBMT), Dpt. Molecular Bioanalytics and Bioelectronics, Arthur-Scheunert-Allee 114-116, 14558 Nuthetal, Germany
1 shared publication Nenad Gajovic-Eichelmann
Department of Molecular Bioanalytics and Bioelectronics, Fraunhofer Institute for Biomedical Engineering, A.-Scheunert-Allee 114, 14558 Bergholz-Rehbrücke, Germany
1 shared publicationPeter M. Schmidt
Department of Molecular Bioanalysis and Bioelectronics, Fraunhofer Institute for Biomedical Engineering, Bergholz-Rehbrücke, Germany
1 shared publication
Latest Publications
- Open Access
- 29 June 2005
- Published by Springer Nature in Journal of Nanobiotechnology
- Vol. 3 (1) , 5
Chemically synthesized zinc finger molecules as nano-addressable probes for double-stranded DNAs
Our experiments describe an alternative method of dsDNA recognition using zinc finger (ZF) molecules which bind DNA specifically and with high affinity. Our aim was to develop zinc finger probes which are able to bind to dsDNA molecules at predetermined sites. In our basic approach we used pairs of complementary oligonucleotides to form dsDNAs, containing one of the three SP1-transcription factor motifs as a zinc finger recognition site. Two zinc finger probes of the SP1 motif were chemically synthesized and modified with a Dy-633 fluorophore. The SP1 peptides were folded into functional zinc fingers using zinc chloride. The addressable dsDNAs were immobilized on optical fibres, and the kinetics and binding rates of the artificial zinc finger probes were measured by a fluorescence detecting device (photomultiplying tube). The two zinc fingers and their corresponding DNA recognition sites served as specific probes and controls for the matching site and vice versa. Our experiments showed that a variety of dsDNA-binding probes may be created by modification of the amino acid sequence of natural zinc finger proteins. Our findings offer an alternative approach of addressing dsDNA molecules, for example for use in a nanoarray device.
- 29 June 2005
- Published by Springer Nature in Journal of Nanobiotechnology
- Vol. 3 (1) , 5
Open AccessChemically synthesized zinc finger molecules as nano-addressable probes for double-stranded DNAs
Our experiments describe an alternative method of dsDNA recognition using zinc finger (ZF) molecules which bind DNA specifically and with high affinity. Our aim was to develop zinc finger probes which are able to bind to dsDNA molecules at predetermined sites. In our basic approach we used pairs of complementary oligonucleotides to form dsDNAs, containing one of the three SP1-transcription factor motifs as a zinc finger recognition site. Two zinc finger probes of the SP1 motif were chemically synthesized and modified with a Dy-633 fluorophore. The SP1 peptides were folded into functional zinc fingers using zinc chloride. The addressable dsDNAs were immobilized on optical fibres, and the kinetics and binding rates of the artificial zinc finger probes were measured by a fluorescence detecting device (photomultiplying tube). The two zinc fingers and their corresponding DNA recognition sites served as specific probes and controls for the matching site and vice versa. Our experiments showed that a variety of dsDNA-binding probes may be created by modification of the amino acid sequence of natural zinc finger proteins. Our findings offer an alternative approach of addressing dsDNA molecules, for example for use in a nanoarray device.
- 13 November 2003
- Published by Springer Nature in Analytical and Bioanalytical Chemistry
- Vol. 378 (1) , 52-53
Real-time analysis on microarrays
- 13 November 2003
- Published by Springer Nature in Analytical and Bioanalytical Chemistry
- Vol. 378 (1) , 52-53
Real-time analysis on microarrays
- 6 March 2003
- Published by Elsevier in Biosensors and Bioelectronics
- Vol. 18 (5-6) , 555-564
Oriented and vectorial immobilization of linear M13 dsDNA between interdigitated electrodes—towards single molecule DNA nanostructures
- 6 March 2003
- Published by Elsevier in Biosensors and Bioelectronics
- Vol. 18 (5-6) , 555-564
Oriented and vectorial immobilization of linear M13 dsDNA between interdigitated electrodes—towards single molecule DNA nanostructures
- 1 September 2001
- Published by Springer Nature in Analytical and Bioanalytical Chemistry
- Vol. 371 (2) , 151-156
Feature-size limitations of microarray technology – a critical review
- 1 September 2001
- Published by Springer Nature in Analytical and Bioanalytical Chemistry
- Vol. 371 (2) , 151-156
Feature-size limitations of microarray technology – a critical review