The authors thank Swiss National Foundation for Science (SNF) for the financial support (grant number P2ELP2_162116 and P300P2_171219), the Darwin College, Erasmus+ program for the financial support (grant number 2018-1-LT01-KA103-046719-15400-P3) and the research leading to these results has received funding from the European Research Council under the European Union&#39;s Seventh Framework Programme (FP7/2007-2013) through the ERC grant PhysProt (agreement number 337969), the Newman Foundation (T.P.J.K.) and The Cambridge Centre for Misfolding Diseases (C.G., M.V., and T.P.J.K.).

1. Aggregation assays on fluorescence plate readers
NOTE: The protocol described here is an example of how to study the aggregation of any protein or peptide by chemical kinetics. In particular, it describes an optimized protocol to study the aggregation of the A&#946;42 peptide, which is involved in the onset and progression of Alzheimer&#8217;s disease58,59. A similar protocol can be adjusted and adopted towards studying the aggregatio...

The authors have nothing to disclose.

The first critical step in this protocol is the preparation of monomeric proteins, such as in the case of A&#946;42 solution described in steps 1.1 and 1.2. It is essential to initiate the aggregation process from a highly pure, monomeric solution, as the presence of oligomeric or aggregated species may result in poor reproducibility of the aggregation kinetics58, and induce artefacts in the AFM measurements (e.g., fibrillar species will be evident at the initial stages of the aggregation), which ...

Over 40 million people worldwide are currently affected by neurodegenerative disorders, such as Alzheimer&#8217;s (AD)1 and Parkinson&#8217;s (PD)2 diseases. More generally, more than fifty pathologies are associated at the molecular level with protein misfolding and aggregation, a process that leads to the proliferation of insoluble fibrillar protein aggregates, known as amyloid deposits3,4. The molecular origins of neurodegeneration and its links with protein conformational changes of proteins leading to amyloid formation, however, remain unclear, in large part because of the high level of heterogeneity, transient nature and nanoscale dimensions of the pathological aggregates4,5.
Highly successful investigations of protein structures in the last several decades have been based widely on the use of bulk methods, including X-ray crystallography, cryo-electron microscopy and nuclear magnetic resonance spectroscopy5,6,7,8,9. Within this class of techniques, infrared (IR) spectroscopy has emerged as a sensitive analytical tool to unravel the chemical properties of biological systems such as proteins8. IR methods allow the quantification of protein secondary and quaternary structural changes during their misfolding and aggregation. In addition, in order to further decipher at the microscopic level the mechanistic details involved in the complex free energy landscapes of protein during their aggregation, a major advance has been the development of chemical kinetics tools to extend to complex self-assembly pathways including amyloid fibrils formation5,6,7,10,11,12. However, bulk spectroscopic methods provide only average information on the heterogeneous ensemble of species present in solution or involved in specific microscopic steps, thus rendering the investigation of the biophysical properties of individual aggregated species challenging at the nanoscale level13,14.
Several microscopy techniques with the capability of operating on scales smaller than the diffraction limit of light have emerged in the last decades. This class of methods includes electron microscopy (EM) and atomic force microscopy (AFM). While scanning electron microscopy (SEM) and transmission electron microscopy (TEM) provide two-dimensional (2D) images of a specimen, AFM has emerged in the last decades as a powerful and versatile technique to study three-dimensional (3D) morphologies, as well as the nanomechanical properties of a sample with sub-nanometer resolution13,14,15,16,17,18,19,20,21,22,23,24,25,26,27. The rationale behind studying protein aggregation via AFM is that this approach enables the investigation of the morphology of individual species present in solution13,14,16,17,19,20,21,25,27,28,29,30,31,32,33,34,35,36,37. In particular, by monitoring the sample as a function of time, AFM allows the investigation of the evolution of the morphology of the species within the sample, which makes it possible to follow and visualize the pathways of amyloid formation23,25,38,39,40,41,42. Furthermore, AFM enables the quantification of structural parameters such as cross-sectional heights and lengths of the individual species present in solution13,19,30,31,32,33,34,35,36,37,40,43,44,45,46,47,48. However, the study of a single biophysical property, such as morphology, is often not sufficient when studying heterogeneous and complex biological systems. AFM, SEM or TEM imaging methods alone do not readily reveal the chemical properties of heterogeneous species of amyloid aggregates at the nanoscale.
A major advance for the analysis of heterogeneous biological samples at this scale has been made recently with the development and application to the field of protein aggregation of infrared nanospectroscopy (AFM-IR)24,26,38,42,49,50,51,52. This innovative method exploits the combination of the spatial resolution of AFM (~1&#8722;10 nm) with the chemical analysis power of IR. The AFM-IR technique is based on the measurement of the photothermal induced resonance effect driven by an IR laser, and on the measurement of the thermal expansion of the sample under investigation by the AFM tip. The sample can be illuminated by the IR laser directly from the top or from the bottom in total internal reflection, similarly as in conventional infrared spectroscopy24,42,52,53. The IR laser can be pulsed with typical frequencies in the order of hundreds of kilohertz (1&#8722;1000 kHz) and tuned over a wide spectral range, typically between 1000&#8722;3300 cm-1. Although the laser source covers an area of ~30 &#181;m diameter, the spatial resolution of the AFM-IR technique is determined nominally by the AFM tip diameter, which detects the local thermal expansion of the system. AFM-IR is well suited to study biological samples because the IR signal is proportional to their thickness up to 1&#8722;1.5 &#181;m, and the resulting IR spectra are generally in agreement with the corresponding FTIR transmission spectra13,54,55. For this reason, established methods of analysis in spectroscopy can be readily applied, such as the study of chemical shifts, band shape change and de-convolution by second derivatives analysis52. Overall, combining the spatial resolution of AFM with the chemical recognition power of IR spectroscopy, AFM-IR enables the simultaneous acquisition of a wide range of morphological, mechanical and chemical properties of a sample at the nanoscale.
Here, we illustrate a protocol for the characterization of the process of protein aggregation that exploits the combination of in vitro fluorescence assays, high-resolution AFM imaging and nanoscale AFM-IR. This combined approach has already excelled in providing detailed results in studying the chemical and structural properties of individual micro-droplets formed by protein aggregates, in the study of liquid-liquid protein phase separation, and in investigating the heterogeneity and biophysical properties of individual aggregated species at the nanoscale23,26,38,45,50,53,56,57.

<table>
	<tbody>
		<tr>
			<td>AFM-IR system</td>
			<td>Anasys Instruments</td>
			<td>nanoIR 2 or 3</td>
			<td>Systems to measure thermal expansion in contact and resonance mode</td>
		</tr>
		<tr>
			<td>Corning 96-well Half Area Black/Clear Bottom Polystyrene NBS Microplate</td>
			<td>Corning</td>
			<td>3881</td>
			<td></td>
		</tr>
		<tr>
			<td>Corning Microplate Aluminium Sealing Tape</td>
			<td>Corning</td>
			<td>6570</td>
			<td></td>
		</tr>
		<tr>
			<td>Double Sided Adhesive Discs</td>
			<td>AGAR Scientific</td>
			<td>AGG3347N</td>
			<td></td>
		</tr>
		<tr>
			<td>FLUOstar Omega</td>
			<td>BMG Labtech</td>
			<td>415-101</td>
			<td>Platereader</td>
		</tr>
		<tr>
			<td>Mica Disc 10mm V1</td>
			<td>AGAR Scientific</td>
			<td>AGF7013</td>
			<td></td>
		</tr>
		<tr>
			<td>Park NX10 AFM system</td>
			<td>Park Systems</td>
			<td>N/A</td>
			<td>Atomic Force Microscope</td>
		</tr>
		<tr>
			<td>Platypus Ultra-Flat Gold Chips</td>
			<td>Platypus Technologies</td>
			<td>AU.1000.SWTSG</td>
			<td></td>
		</tr>
		<tr>
			<td>PPP-NCHR-10 cantilevers</td>
			<td>Park Systems</td>
			<td>PPP-NCHR-10</td>
			<td></td>
		</tr>
		<tr>
			<td>Protein LowBind Tubes, 2.0mL</td>
			<td>Eppendorf</td>
			<td>30108132</td>
			<td></td>
		</tr>
		<tr>
			<td>Silicon gold coated cantilevers</td>
			<td>Anasys Instruments</td>
			<td>PR-EX-nIR2</td>
			<td></td>
		</tr>
		<tr>
			<td>SPM Specimen Discs 12mm</td>
			<td>AGAR Scientific</td>
			<td>AGF7001</td>
			<td></td>
		</tr>
	</tbody>
</table>

characterizing individual protein aggregates by infrared nanospectroscopy and atomic force microscopy

The phenomenon of protein misfolding and aggregation results in the formation of highly heterogeneous protein aggregates, which are associated with neurodegenerative conditions such as Alzheimer&#8217;s and Parkinson&#8217;s diseases. In particular low molecular weight aggregates, amyloid oligomers, have been shown to possess generic cytotoxic properties and are implicated as neurotoxins in many forms of dementia. We illustrate the use of methods based on atomic force microscopy (AFM) to address the challenging task of characterizing the morphological, structural and chemical properties of these aggregates, which are difficult to study using conventional structural methods or bulk biophysical methods because of their heterogeneity and transient nature. Scanning probe microscopy approaches are now capable of investigating the morphology of amyloid aggregates with sub-nanometer resolution. We show here that infrared (IR) nanospectroscopy (AFM-IR), which simultaneously exploits the high resolution of AFM and the chemical recognition power of IR spectroscopy, can go further and enable the characterization of the structural properties of individual protein aggregates, and thus offer insights into the aggregation mechanisms. Since the approach that we describe can be applied also to the investigations of the interactions of protein assemblies with small molecules and antibodies, it can deliver fundamental information to develop new therapeutic compounds to diagnose or treat neurodegenerative disorders.

A representative time course of A&#946;42 aggregation, as measured by the ThT fluorescence assay, is shown in Figure 1. The aggregation process is commonly characterized by a sigmoidal curve, where a lag phase is initially observed, and is followed by a steep growth phase, before the curve reaches a plateau when an equilibrium steady state is reached6,7,58. It is essential to ensure that an optimize...

Watch this Scientific Journal Video about Characterizing Individual Protein Aggregates by Infrared Nanospectroscopy and Atomic Force Microscopy at JoVE.com

Characterizing Individual Protein Aggregates by Infrared Nanospectroscopy and Atomic Force Microscopy

We describe the application of infrared nanospectroscopy and high-resolution atomic force microscopy to visualize the process of protein self-assembly into oligomeric aggregates and amyloid fibrils, which is closely associated with the onset and development of a wide range of human neurodegenerative disorders.

The phenomenon of protein misfolding and aggregation results in the formation of highly heterogeneous protein aggregates, which are associated with ...

Methods based on atomic force microscopy make it possible to characterize biomolecular processes at the nano scale with morphological chemical or structural resolution, finally opening a new front window of observation on biology. Single molecule methods enable probing highly heterogeneous systems, a feature which is particularly relevant for understanding protein aggregation. By combining single molecules with back approaches, we can obtain fundamental information about the behavior of proteins, their links with human disease and design pharmacological interventions which can be successful.Furthermore, this method can be successfully applied to study the chemical and structural properties of biomaterials for drug delivery, applications and other biotechnological purposes. It may be challenging initially to set the correct AFM parameters for high resolution and it's easy to set up your AFM while measuring your fibrillar aggregates. 30 minutes before the AFM imaging, turn on the AFM system and click set up and probe.In the probe change window, click next to prepare Z focus stage. Turn off the AFM beam switch if it is on and unlock the dovetail locks. Disconnect the head from the system and in the probe change window, click next.Mount the AFM cantilever on the probe holder. Connect the head to the system and lock the dovetail locks. Turn on the AFM laser beam switch and in the probe change window, click next.In the pop up window, click no if the cantilever type did not change and adjust the optical alignment knobs to find the cantilever. Adjust the focus onto the cantilever and click next. In the pop up window, click yes if the focus is on the cantilever.Use the detection laser beam knobs to position the laser beam at the end of the cantilever. Use the deflected laser beam knobs to maximize the total signal measured by the four quadrant photo diode to at least greater than one volt. In the probe change window, click next and close.After waiting 15 minutes for the cantilever to reach thermal stability, readjust the position of the deflected laser beam on the position sensitive photo diode if necessary. Click NCM sweep, select the desired amplitude of oscillation, click use phase and click auto. Tune the cantilever close to the maximum of its first free resonance of oscillation to approximately 300 kilohertz for a cantilever with a spring constant of 40 newtons per meter.Place the sample on the sample holder. Click scan area and set the resolution to between 256 by 256 and 1024 by 1024 pixels and then set the scan size and the pixel number. Set the scanning rate to 0.3 to one hertz for a scan area of one by one to five by five micrometers squared.Focus the optical view on the sample and click approach to approach the sample surface. Next, click lift 100 micrometers to raise the AFM tip 100 micrometers above the surface of the sample and click expand on the optical image of the sample. Click the focus stage bar to focus the view on the surface of the sample and use the arrows to move in the region of the sample of interest.Click approach to engage the surface and click line scan to check if the tip is following the surface well. Adjust the set point as necessary. Then click scan to begin imaging the sample surface, maintaining a constant regime of phase change not exceeding delta 20 during the imaging to avoid a large imaging force and to maintain consistency between independent samples.For IR nanospectroscopy imaging, 30 to 60 minutes before the analysis, turn on the AFM IR system and the IR laser. Open the built in software to control the instrument and click file and new to open a new nano IR file. Click initialize to start the AFM IR system and open the instrument cover.Mount a silicone gold coated probe with a nominal radius of 30 nanometers and a spring constant of 0.2 newtons per meter onto the AFM IR system to measure the sample in contact mode. Click load in the AFM probe section and next. Use the focus on probe arrows to focus the camera on the cantilever and use the tip to crosshairs to place the crosshair at the end of the cantilever.Rotate the knobs controlling the position of the detection laser to position the laser at the end of the cantilever. Rotate the laser knobs to detect and maximize the sum measured by the four quadrant photo diode to a value greater than three volts. Rotate the deflection knob to adjust the cantilever deflection to minus one volt and click next.Then close the cover of the instrument. Use the focus on probe arrows to focus the camera on the sample and tip to crosshairs arrows to move in the region of interest of the sample. Click next and engage.In the microscope window, select height for morphology, amplitude two for the IR absorption and PLL frequency to map the tip to sample contact resonance. In the AFM scan section, set the parameters as demonstrated for the AFM imaging and click scan to acquire a morphology map. When the morphology mapping is finished, in the microscope window, click the height map to position the probe on the top of one aggregate.In the nano IR section, click start IR to illuminate the sample with the IR laser. To focus the infrared laser on the cantilever, click optimize and enter 1655 centimeters for the wavenumber. Click add and scan to determine the IR laser position and click update and okay to align its position with the cantilever.In the general section, enter a wavenumber for which a high absorbance in the relative field is expected and deactivate the band pass filter option. Click start IR then check the meter reading and the FFT of the cantilever response. In the FFT window, move the green cursor to read the resonance frequency of the cantilever.A typical value of the FFT of the resonance of the cantilevers is around 200 kilohertz. Enter the generated resonance frequency value in the general section in the frequency center field and use a frequency window of 50 kilohertz. Click laser pulse tune window to select the resonance enhanced mode and set a pulse rate of 222 kilohertz, a tune range of 50 kilohertz and a laser duty cycle of 5%Click acquire to sweep the pulse rate of the laser.Use the cursor to tune the laser pulse to the frequency of the mechanical response of the thermal expansion of the sample absorbing the IR light. Then select phase locked loop to monitor the contact resonance between the sample and the tip and click zero. For other chemical properties at the nano scale, track the contact resonance during the spectra acquisition to ensure that the sample spectrum is not affected by overheating and softening.Select enable to track the sample to tip contact resonance and select an integral gain of 0.5 and a proportional gain of 10 then click OK.In the optimize window, click the wavelength and scan to locate the IR laser for at least three wavenumbers corresponding to major absorbance bands of the sample and for at least one wavenumber for each chip of the laser. Click tools, IR background calibration and new, and set the wavenumbers to between 1200 and 1800 centimeters. Set the backgrounds to average to one, the duty cycle of 5%and the sweep speed to 100 centimeters squared.Click acquire to measure the IR laser background for normalization of the measured nano scale localized spectra, save the file and close the window. In the IR spectra settings, select an IR spectrum resolution between one and four centimeters and a number of co-averages of at least 64 times. Then click acquire to measure a nano scale localized IR spectrum in the protein range.To acquire a nano scale resolved chemical map, select 1655 centimeters and IR imaging and click scan in the AFM scan window. When the mapping is completed, save the measurements. Then use the built in AFM image processing software to analyze the acquired maps of morphology, contact resonance and chemistry and nano scale localized spectra.It is a critical step to obtain a highly pure monomeric solution as the presence of aggregated species may result in poor reproducibility of kinetics and introduce artifacts in your measurements. A fundamental factor for successfully studying biological samples which have high heterogeneity is the correct the position of solid substrates. Microfluidic spray deposition can be exploited instead of manual one in order to preserve the sample architecture and heterogeneity.These methods pave the way for unraveling the chemical structure and properties of individual biomolecules and their interactions in physiological and native liquid environment.

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JoVE Journal

Biochemistry

9.6K visualizações.  University of Cambridge. Métodos baseados na microscopia de força atômica possibilitam caracterizar processos biomoleculares na escala nano com resolução química ou estrutural morfológica, finalmente abrindo uma nova janela frontal de observação sobre biologia. Métodos de molécula única permitem sondar sistemas altamente heterogêneos, uma característica que é particularmente relevante para a compreensão da agregação de proteínas. Combinando moléculas únicas com abordagens traseiras, podemos obter...