Development of versatile molecular-size machine systemswill be the cornerstone of future technologies in biology and medicine. The goal of this project is to develop the first practical nanomachine design by integrating an active biological molecule of a molecular motor protein with artificially engineered components. The construct will be a molecular-size machine belonging to a new class of semi-artificialnanodevices, which we recently introduced. It will perform super-fast labeling of specific DMAbreaks via covalent attachment of fluorescent markers. After self-assembly, the machine will use its own material to fabricate two detector units. In the presence of blunt-ended DNA breaks of DNase I type (bearing 5' PO4) or DNase II type (bearing 5' OH), the detector units will selectively attach to their target DNA ends and will label them with either red or green fluorophores. The described construct will be the first nanosensor detecting two types of specific DNA breaks in fixed tissue sections and a super-fast sensor detecting DNA damage and apoptosis in live non-fixed cells within seconds.
Specific Aims of the project are: 1. To design and test a semi-artificial nanomachine capable of super- fast detection of different types of DNA damage in solubilized DNA. 2. To develop a biomedical application of the newly designed nanomachine employing it as a nanosensor for detection of two major types of apoptosis in fixed tissues, based on labeling of DNase I and II type DNA breaks. 3. To develop a biomedical application of the newly designed nanomachine employing it as a super-fast nanosensor for detection of DNA damage and apoptosis in non-fixed live cells.
In Aim1 we will use model systems with specific amounts of DNA breaks in solution to test selectivity, specificity and speed of detection.
In Aim 2 we will apply our new construct to fixed tissue sections and will develop its application as a nanosensor for in situ detection of apoptosis.
In Aim 3 we will develop an application of our construct as a super-fast sensor detecting apoptosis in live cells without their fixation. The semi-artificial nanomachine will exemplify a new bionic approach to the design of super-fast molecular- size devices and will be a unique tool for detection of DNA damage and apoptosis useful in biological and medical research.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21EB006301-03
Application #
7369823
Study Section
Special Emphasis Panel (ZRG1-BCMB-R (50))
Program Officer
Korte, Brenda
Project Start
2006-04-01
Project End
2010-03-31
Budget Start
2008-04-01
Budget End
2010-03-31
Support Year
3
Fiscal Year
2008
Total Cost
$154,633
Indirect Cost
Name
Baylor College of Medicine
Department
Neurosurgery
Type
Schools of Medicine
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030
Didenko, Vladimir V (2017) Zebra Tail Amplification: Accelerated Detection of Apoptotic Blunt-Ended DNA Breaks by In Situ Ligation. Methods Mol Biol 1644:167-177
Minchew, Candace L; Didenko, Vladimir V (2014) Assessing phagocytic clearance of cell death in experimental stroke by ligatable fluorescent probes. J Vis Exp :
Didenko, Vladimir V (2014) Selective detection of phagocytic phase of apoptosis in fixed tissue sections. Methods Mol Biol 1094:159-66
Minchew, Candace L; Didenko, Vladimir V (2014) Nanoblinker: Brownian motion powered bio-nanomachine for FRET detection of phagocytic phase of apoptosis. PLoS One 9:e108734
Minchew, Candace L; Didenko, Vladimir V (2014) Selective transport of cationized fluorescent topoisomerase into nuclei of live cells for DNA damage studies. Methods Mol Biol 1094:167-75
Minchew, Candace L; Didenko, Vladimir V (2012) In vitro assembly of semi-artificial molecular machine and its use for detection of DNA damage. J Vis Exp :e3628
Minchew, Candace L; Didenko, Vladimir V (2011) Fluorescent probes detecting the phagocytic phase of apoptosis: enzyme-substrate complexes of topoisomerase and DNA. Molecules 16:4599-614
Hornsby, Peter J; Didenko, Vladimir V (2011) In situ ligation: a decade and a half of experience. Methods Mol Biol 682:49-63
Didenko, Vladimir V (2011) In situ ligation simplified: using PCR fragments for detection of double-strand DNA breaks in tissue sections. Methods Mol Biol 682:65-75
Didenko, Vladimir V (2011) In situ labeling of DNA breaks and apoptosis by T7 DNA polymerase. Methods Mol Biol 682:37-48

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