Single biomolecule studies using optical tweezers

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Single biological molecule studies enable to probe and visualize exciting details of the events in physiological in vivo processes. The basic underlying question of this dissertation is to understand biological processes at a single molecule level. In contrast to ensemble techniques, advances in single molecule manipulation (e.g. optical and magnetic tweezers, atomic force microscopy) and / or fluorescence techniques allow to investigate the properties of individual molecules in real time with a possibility to change external conditions (buffers) in situ and modulate inter- and intra-molecular interactions. This thesis reports the application of a single molecule technique, dual beam optical tweezers, for the study of single biomolecules. A range of single molecule systems was investigated such as i)VirE2 protein DNA machinery, ii) DNA-surfactant, EtBr (ethidium bromide), SYBR® Green-DNA interactions and iii) dsDNA denaturation studies. In addition the development of the present experimental setup is described to enable combined force measurement as well as single molecule fluorescence studies. The presented biomolecular results provide new and complementary information on the different biological systems demonstrating the diversity of experiments that can be performed on single DNA molecules using optical tweezers. Chapter one gives a brief introduction to optical tweezers, describes how optical tweezers work, the physics behind it, details of the experimental setup and the method of force calibration required in micromanipulation. Optical tweezers have opened exciting avenues of research, especially in biology. Biologists will be able to investigate the nature of molecular machines one by one, and infer from their behavior those properties common to the population. In chapter 2, we show how optical tweezers were employed to study the change in the mechanical properties of single DNA molecules upon binding of small agents. The first part of this chapter reports on the changes in mechanics of single dsDNA in the presence of cationic and anionic surfactants (used as non-viral vectors in gene therapy). The second part describes the interaction of DNA binding ligands (SYBR® Green, EtBr) with individual DNA strands. Agrobacterium tumefaciens (AT), a Gram-negative bacterium, evolved a complex and unique mechanism to transfer a long single stranded DNA (ssDNA) molecule from its cytoplasm to the eukaryotic host plant cell nucleus. Central to this mechanism, chapter 3 discusses the results of the measurements on VirE2 protein interacting with single stranded DNA (ssDNA). VirE2 protein is a multifunctional protein from AT that coat the transferred-ssDNA (T-DNA), interacts with host factors assisting nuclear import of the complex, forms channels in lipid bilayers and displays a highly cooperative binding to ssDNA. The biological findings are presented in a new generic model which can be used to explain how generation of forces helps bacterial DNA to enter the plant cell based on our single molecule data. Single molecule dsDNA denaturation, relevant in many molecular biological experiments, induced by NaOH and mechanical pulling are studied in chapter 4. Here optical tweezers experiments give access to the ‘melting’ of hydrogen bonds by mechanical forces or alkali denaturation (NaOH) of dsDNA in real time. The mechanical stability and the transition of dsDNA to ssDNA is investigated at different ionic strength as well as in buffers. Fluorescent images of single λ DNA labeled with SYBR® Green were observed up to forces ≥ 65 pN and indicate a B-DNA to S −DNA transition. Chapter 5 describes the implementation of single-molecule fluorescence detection (SMF) in optical tweezers. The design and instrumental capabilities of optical tweezers combined with SMF are discussed in detail. The development of this instrument provides a worldwide unique experimental setup and opens up new possibilities in the studies of complex biological systems. Finally chapter 6 summarizes the results of this thesis and discusses future experimental applications. The appendices provide further details for DNA sample preparation, molecular biology and chemical surface activation recipes, an instruction manual for the setup and the list of currently published papers.