Paper
10 September 2004 Nanoprocessing of DNA with femtosecond laser
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Abstract
Sequence specific cutting of DNA is a standard method in molecular biology. This cutting is realized with enzymes which have a defined recognition sequence and cutting sequence. Therefore one can manipulate only sequences for which an enzyme is available. With current physical methods (AFM) any sequences can be cut, but the precise sequence specific and highly parallel cutting is not possible. Near infrared (NIR) femtosecond laser systems have been used to optically knock out genomic regions of highly condensed DNA in human chromosomes as well as of single expanded (stretched) DNA molecules. Working with 80 MHz laser pulses at 800 nm of low 2 nJ pulse energy but at high TW/cm2 light intensities, multiphoton ionization and optical breakdown (OB) resulted in highly precise material ablation with sub-100 nm cut sizes. This is far below the diffraction-limited spot size. A minimum FWHM cut size of 65 nm was achieved in the case of the nanodissection of a laser-treated stretched λ-DNA (48kb) molecule which corresponded to 200 optically knocked out bases. By the use of metal nanoparticles as energy coupling objects for fs laser radiation we expect a specific highly local destruction effect within the DNA molecule (cut). Thereby, a sequence-specific binding of DNA nanoparticle complexes along the target DNA is a fundamental condition. The effect of laser exposure on DNA and DNA-nanoparticle complexes are presented.
© (2004) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Karsten Koenig, Frank Garwe, Andrea Czaki, Gunther Maubach, Iris Riemann, and Wolfgang Fritzsche "Nanoprocessing of DNA with femtosecond laser", Proc. SPIE 5462, Biophotonics Micro- and Nano-Imaging, (10 September 2004); https://doi.org/10.1117/12.545730
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KEYWORDS
Molecules

Nanoparticles

Femtosecond phenomena

Gold

Molecular lasers

Laser cutting

Particles

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