Kinetic binding analysis of aptamers targeting HIV-1 proteins by a combination 
of a microbalance array and mass spectrometry (MAMS)

Gronewold, T. M.; Baumgartner, A.; Hierer, J.; Sierra, S.; Blind, M.; Schäfer, F.; Blümer, J.; Tillmann, T.; Kiwitz, A.; Kaiser, R.; Zabe-Kühn, M.; Quandt, E.; Famulok, M.

doi:10.1021/pr900265r

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Kinetic binding analysis of aptamers targeting HIV-1 proteins by a combination of a microbalance array and mass spectrometry (MAMS)

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http://www.ncbi.nlm.nih.gov/pubmed/19469583
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http://pubs.acs.org/doi/pdfplus/10.1021/pr900265r
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Zitation

Gronewold, T. M., Baumgartner, A., Hierer, J., Sierra, S., Blind, M., Schäfer, F., et al. (2009). Kinetic binding analysis of aptamers targeting HIV-1 proteins by a combination of a microbalance array and mass spectrometry (MAMS). Journal of proteome research, 8(7), 3568-77. doi:10.1021/pr900265r.

Zitierlink: https://hdl.handle.net/11858/00-001M-0000-0028-644B-8

Zusammenfassung

An enhanced chip-based detection platform was developed by integrating a surface acoustic wave biosensor of the Love-wave type with protein identification by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-ToF MS). The system was applied to characterize the interaction of aptamers with their cognate HIV-1 proteins. The aptamers, which target two proteins of HIV-1, were identified using an automated in vitro selection platform. For aptamers S66A-C6 and S68B-C5, which target the V3 loop of the HIV-1 envelope protein gp120, KD values of 406 and 791 nM, respectively, were measured. Aptamer S69A-C15 was shown to bind HIV-1 reverse transcriptase (HIV-1 RT) with a KD value of 637 nM when immobilized on the biosensor surface. HIV-1 RT was identified with high significance using MALDI-ToF MS even in crude protein mixtures. The V3-loop of gp120 could be directly identified when using chip-bound purified protein samples. From crude protein mixtures, it could be identified indirectly with high significance via its fusion-partner glutathione-S-transferase (GST). Our data show that the combination of the selectivity of aptamers with a sensitive detection by MS enables the reliable and quantitative analysis of kinetic binding events of protein solutions in real time.