Tobias F. Bartsch

Detecting Sequential Bond Formation Using Three-Dimensional Thermal Fluctuation Analysis

We present a novel experimental method that solves two key problems in nondestructive mechanical studies of small biomolecules at the single-molecule level, namely the confirmation of single-molecule conditions and the discrimination against nonspecific binding. A biotin-avidin ligand-receptor couple is spanned between a glass slide and a 1 microm latex particle using short linker molecules. Optical tweezers are used to initiate bond formation and to follow the particles thermal position fluctuations with nanometer spatial and microsecond temporal resolution. Here we show that each step in the specific binding process leads to an abrupt change in the magnitude of the particles thermal position fluctuations, allowing us to count the number of bonds formed one by one. Moreover, three-dimensional position histograms calculated from the particles fluctuations can be separated into well-defined categories reflecting different binding conditions (single specific, multiple specific, nonspecific). Our method brings quantitative mechanical single-molecule studies to the majority of proteins, paving the way for the investigation of a wide range of phenomena at the single-molecule level.

Direct observation of intermediate states in model membrane fusion.

We introduce a novel assay for membrane fusion of solid supported membranes on silica beads and on coverslips. Fusion of the lipid bilayers is induced by bringing an optically trapped bead in contact with the coverslip surface while observing the bead’s thermal motion with microsecond temporal and nanometer spatial resolution using a three-dimensional position detector. The probability of fusion is controlled by the membrane tension on the particle. We show that the progression of fusion can be monitored by changes in the three-dimensional position histograms of the bead and in its rate of diffusion. We were able to observe all fusion intermediates including transient fusion, formation of a stalk, hemifusion and the completion of a fusion pore. Fusion intermediates are characterized by axial but not lateral confinement of the motion of the bead and independently by the change of its rate of diffusion due to the additional drag from the stalk-like connection between the two membranes. The detailed information provided by this assay makes it ideally suited for studies of early events in pure lipid bilayer fusion or fusion assisted by fusogenic molecules.

Nanoscopic imaging of thick heterogeneous soft-matter structures in aqueous solution.

Precise nanometre-scale imaging of soft structures at room temperature poses a major challenge to any type of microscopy because fast thermal fluctuations lead to significant motion blur if the position of the structure is measured with insufficient bandwidth. Moreover, precise localization is also affected by optical heterogeneities, which lead to deformations in the imaged local geometry, the severity depending on the sample and its thickness. Here we introduce quantitative thermal noise imaging, a three-dimensional scanning probe technique, as a method for imaging soft, optically heterogeneous and porous matter with submicroscopic spatial resolution in aqueous solution. By imaging both individual microtubules and collagen fibrils in a network, we demonstrate that structures can be localized with a precision of ∼10 nm and that their local dynamics can be quantified with 50 kHz bandwidth and subnanometre amplitudes. Furthermore, we show how image distortions caused by optically dense structures can be corrected for.

Power spectral density integration analysis and its application to large bandwidth, high precision position measurements

High precision position measurements often involve the detection of a laser beam that interacts with various components of an experimental setup. In order to achieve the highest precision, instabilities that contribute to a decrease in precision must be identified and quantified. Instabilities include fluctuations in the laser power, fluctuations in the laser pointing and fluctuations in the phase, as well as vibrating mechanical components that are susceptible to excitations and drift. Instabilities lead to unwanted resonances and band structures in the power spectral density of the detector signals. Typically, the most important instabilities are identified by the magnitude and location of resonances or bands in the power spectral density. However, power spectral density plots can be misleading if the width or shape of a resonance or a band are not correctly accounted for. This is especially true for measurements that span a large bandwidth. Here, we discuss Power Spectral Density Integration Analysis as a more intuitive and accurate method for identifying and quantifying instabilities. Resonances and bands are readily identified as step-like features with heights that correctly represent their contribution to the error in the position measurement.

Resolving Filament Level Mechanics in Collagen Networks using Activity Microscopy

Collagen is the most abundant protein in humans and the primary component of the extracellular matrix, a meshwork of biopolymer networks, which provides structure and integrity to tissues. Its mechanical properties profoundly influence the fate of cells. The cell-matrix interaction, however, is not well understood due to a lack of experimental techniques to study the mechanical interplay between cells and their local environment. Here we introduce Activity Microscopy, a new way to visualize local network mechanics with single filament resolution. Using collagen I networks in vitro, we localize fibril positions in two-dimensional slices through the network with nanometer precision and quantify the fibrils’ transverse thermal fluctuations with megahertz bandwidth. Using a fibril’s thermal fluctuations as an indicator for its tension, we find a heterogeneous stress distribution, where “cold” fibrils with small thermal fluctuations surround regions of highly fluctuating “hot” fibrils. We seed HeLa cells into collagen networks and quantify the anisotropy in the propagation of their forces.