Patent Application
20230109927
The present invention relates to characterization of gene therapy vectors and viral particles, and more particularly to a method of determining the levels of empty and full capsids in a viral particle preparation.
Recombinant viruses show great promise and utility as a vehicle to deliver therapeutic nucleic acids for gene therapy applications. A number of different recombinant viruses are used in these gene therapy applications based on a number of factors including the size of the nucleic acid to be delivered, the target cell or tissue to deliver the nucleic acid, the need for short or long term expression of the therapeutic nucleic acid, and integration of the therapeutic nucleic acid into the recipient's genome. Examples of viruses used in gene therapy applications include adeno-associated virus (AAV), adenovirus, lentivirus and herpes simplex virus (HSV). Also non-viral vectors can be used for delivery of nucleic acids in gene therapy. Examples of such vectors include liposomes and other lipoplexes (see e.g. US2009305409, U.S. Pat. Nos. 6,749,863, 6,071,533 and 6,303,378, hereby incorporated by reference in their entireties), polymersomes and polyplexes (see e.g. US20110206751, US2017000743 and US2011151013, hereby incorporated by reference in their entireties), as well as inorganic and organic nanoparticles.
Polymerase Chain Reaction (PCR) is a common technique for determining the genome content of adeno-associated viruses (AAV), and Analytical Ultracentrifugation (AUC) (see e.g. US2018180525, hereby incorporated by reference in its entirety) is commonly used for estimating the level of empty capsids (containing only the protein capsids with no DNA) and full capsids (containing both protein and DNA). Also spectrophotometric methods (e.g. WO2019212922, hereby incorporated by reference in its entirety) have been used to determine levels of empty and full capsids. However, these techniques require multiple steps with complicated procedures that are time-consuming and relatively low-throughput. More efficient and better quantitative techniques are thereby desirable for sample screening, in-process sample analysis for process control and monitoring, and final product concentration determination and stability monitoring.
Accordingly, there is a need for simple and rapid methods to characterize virus preparations with respect to empty and full capsids. Likewise, there is a need for simple and rapid methods to characterize non-viral vectors with respect to their being loaded or not with the intended nucleic acid.
One aspect of the invention is to provide a method of distinguishing empty and full capsids in a virus preparation. This is achieved with a method comprising the steps of:
a) providing a preparation of viral particles;
b) subjecting the preparation to interferometric scattering mass spectrometry (ISCAMS), in an interferometric scattering microscope, to generate mass distribution data for the viral particles;
c) determining the levels of empty capsids and capsids comprising a genome among the viral particles from the mass distribution data.
One advantage is that the method is rapid (a few minutes) and simple and has a high accuracy. A further advantage is that the method is able to measure particles from samples where there is a complex mixture of differently sized particles present; smaller particles are not “hidden” by the presence of larger particles. A yet further advantage is that minimal amounts of sample (<˜20 μl) are needed. These advantages make the method a particularly useful technology for at-line process analytical testing (PAT).
A second aspect of the invention is to provide a method of distinguishing non-viral gene therapy vectors loaded with a nucleic acid from vectors which are not loaded with a nucleic acid. This is achieved with a method comprising the steps of:
a) providing a preparation of non-viral gene therapy vectors;
b) subjecting the preparation to interferometric scattering mass spectrometry (ISCAMS), in an interferometric scattering microscope, to generate mass distribution data for the vectors;
c) determining the levels of vectors loaded with a nucleic acid and vectors which are not loaded with nucleic acid from the mass distribution data.
Further suitable embodiments of the invention are described in the dependent claims.
a) in PBS buffer+130 mM NaCl, 0.001% (v/v) Pluronic F-188
b) in PBS buffer+130 mM NaCl, 0.001% (v/v) Pluronic F-188 (replicate)
c) in 20 mM TRIS buffer pH 8.5, no salt
d) in 20 mM TRIS buffer pH 8.5, no salt (replicate)
As used herein, the terms “comprises,” “comprising,” “containing,” “having” and the like can have the meaning ascribed to them in U.S. patent law and can mean “includes,” “including,” and the like; “consisting essentially of” or “consists essentially” likewise has the meaning ascribed in U.S. patent law and the term is open-ended, allowing for the presence of more than that which is recited so long as basic or novel characteristics of that which is recited is not changed by the presence of more than that which is recited, but excludes prior art embodiments.
In one aspect, the present invention discloses a method of characterizing a preparation of viral particles comprising the steps of:
a) Providing a preparation of viral particles. The preparation can e.g. be a preparation of viral particles intended to be used as viral vectors for cell/gene therapy but they can also be intended to be used e.g. as a vaccine antigen. In particular, they can be selected from the group consisting of adeno-associated virus (AAV), adenovirus (AV), Herpes simplex virus (HSV), retroviruses, lentiviruses and alphaviruses, with preference for AAV. The viral particles can suitably be recombinant, with an engineered genome in the capsids and the preparation may also include empty capsids. The preparation may comprise at least 5×108 viral particles per ml preparation, such as at least 1×109 viral particles per ml preparation, 5×108-1×1013 or 1×109-1×1012 viral particles per ml preparation. The preparation can suitably comprise a buffer, e.g. a PBS or Tris buffer, which may have a pH of 3-9, such as 6-8.5 or 7-8.5, and which may further comprise a salt, e.g. NaCl. Further, the preparation may comprise a dispersant, such as a poloxamer (ethylene oxide-propylene oxide block copolymers). Examples of poloxamer dispersants can be poloxamer 188 (Cas No. 9003-11-6), e.g. Pluronic F-188 (BASF) or Pluronic F-68. The preparation can typically be a cell culture fluid (e.g. a cell lysate), a partially purified cell culture fluid/cell lysate or a purified suspension of viral particles originating from a cell culture fluid/cell lysate.
b) Subjecting the preparation to interferometric scattering mass spectrometry (ISCAMS), in an interferometric scattering microscope, to generate mass distribution data for the viral particles. In this step, the intensity of scattered light from individual virus particles on a surface can be measured and the mass distribution data calculated from a scattered light intensity distribution. The interferometric scattering microscope can be constructed as disclosed in US20190004299, hereby incorporated by reference in its entirety, and it can in particular be a Refeyn OneMP microscope, commercially available from Refeyn Ltd., Oxford, UK. In this instrument a sample of the preparation is placed onto a glass slide (which may be functionalized to bind or exclude certain biomolecules) and the slide placed above the lens of the microscope. The instrument uses laser light focused on the surface of the slide and the point-spread function of molecules/particles are observed as they come close to the surface. The equipment can distinguish particles as they bind and unbind from the surface, as well as “wobbling” across the surface. To clearly distinguish these particles the software divides consecutive frames of the movie to provide “ratiometric imaging”. The microscope detects the interference between the reflected and scattered light from single molecules/particles. The intensity, or contrast, of this interference point then correlates to the density of the molecule. The density of proteins remains constant over quite a range, as does the density of DNA, and this scales with particle mass. So, with the help of calibration reference standards the contrast of the spots can be used to calculate the mass of the particles. The surface holding the virus particles can suitably be a glass surface, such as a glass slide or coverslip. It can be a non-modified glass surface or it can be chemically modified, e.g. with functional silanes. The chemical modification can also involve derivatization with ligands capable of binding the viral particles, e.g. llama antibody ligands that have been shown to bind AAV of serotypes 1, 2, 3, 4 and 5 (as used in AVB Sepharose High Performance, GE Healthcare). With regard to the construction of the microscope, it can typically comprise:
a sample holder for holding a sample in a sample location;
an illumination source arranged to provide illuminating light;
a detector;
an optical system arranged to direct illuminating light onto the sample location and further arranged to collect output light in reflection, the output light comprising both light scattered from the sample location and illuminating light reflected from the sample location, and yet further arranged to direct the output light to the detector; and
a spatial filter positioned to filter the output light, the spatial filter being arranged to pass output light but with a reduction in intensity that is greater within a predetermined numerical aperture than at larger numerical apertures. The sample holder can suitably comprise a surface (as discussed above) and viral particles the interact with the surface.
c) Determining the levels of empty capsids and capsids comprising a genome (full capsids) among the viral particles from the mass distribution data. The empty and full capsids show up as distinct peaks in the mass distribution and the relative numbers can be obtained by integrating the peaks or adding the counts in each peak when presented as a histogram. The viral particles are much larger than essentially all particles within typical cell lysates, so the viral particle peaks can clearly be distinguished from other cellular protein/DNA contaminants.
In some embodiments, the method is performed for at-line testing in a process for manufacturing viral vectors. It can suitably be used in process analytical technology (PAT), e.g. wherein at least one process parameter is adjusted when a predetermined ratio of empty capsids to full capsids is reached. In this case, the samples may be complex, i.e. with many other biomolecules present. In particular, the method can be applied in conjunction with a chromatography step, e.g. where the method is performed on an eluate or a flowthrough from a chromatography step. The process parameter can then e.g. be the amount of a viral vector preparation loaded on a chromatography column or device. If the ratio of empty to full capsids is too high in a chromatographic cycle, the amount loaded can be decreased in a subsequent cycle. To increase the selectivity for the viral vectors, e.g. AAV vectors, it can be advantageous to use surfaces derivatized with ligands that selectively bind the vectors. It can also be advantageous to use diluted samples to reduce the total biomolecule concentration.
In a second aspect, the invention discloses a method of distinguishing non-viral gene therapy vectors loaded with a nucleic acid from vectors which are not loaded with a nucleic acid, comprising the steps of:
a) Providing a preparation of non-viral gene therapy vectors. The vectors can e.g. be liposomes or other lipoplexes, polymersomes or polyplexes, as well as inorganic and organic nanoparticles. The vectors can suitably have diameters below 1000 nm, such as below 500 nm, below 200 nm or below 100 nm. They can e.g. have volume-weighted average diameters of 10-1000 nm, such as 10-500 nm, 10-200 nm, 10-100 nm, 20-500 nm, 20-500 nm or 20-100 nm.
b) Subjecting the preparation to interferometric scattering mass spectrometry (ISCAMS), in an interferometric scattering microscope as discussed above, to generate mass distribution data for the vectors. As discussed above, the intensity of scattered light from individual vectors present on a surface may be measured and the mass distribution data are calculated from a scattered light intensity distribution. The vectors can be present on a glass surface, such as a glass slide or coverslip surface. This glass surface may or may not be chemically modified, in particular with ligands capable of binding the vectors. In case the vectors have diameters above 20 nm, such as above 50 nm or above 100 nm, the interferometric scattering microscope may be fitted with a high wavelength laser, such as a laser emitting light of above 600 nm, such as above 700 nm, 600-1000 nm, 600-800 nm or 700-800 nm.
c) Determining the levels of vectors loaded with a nucleic acid and vectors which are not loaded with nucleic acid from the mass distribution data.
The experiments were carried out with a Refeyn OneMP microscope, where a sample was placed on a non-functionalized glass slide above the microscope lens. The ISCAMS analysis was carried out according to the microscope instructions and the data were plotted as particle counts vs. particle mass histograms. For the peaks identified, average mass, standard deviation and total peak count were calculated.
We tested purified AAV-5 samples using non-functionalized glass slides. In our setup it was not possible to determine absolute counts of the AAV titer, this would require functionalizing the surface such that AAV particles are only counted once during the sampling time. This is possible using existing or new affinity ligands against AAV, but was not explicitly tested here.
The detection method enables mass photometry to measure the mass of the AAV capsids, and so distinguish empty and full AAV virions. This is achieved without labelling and, as the AAV are much larger than almost all particles within typical cell lysates, the AAV can clearly be distinguished from other cellular protein/DNA contaminants. We found AAV particles generally did not bind to the glass surface, so could be counted many times. This was of benefit as long-movie collection times could be used to ensure a high number of particle counts. However, whilst this method provides a ratiometric comparison for empty:full particles it does not provide an absolute count of AAV titres. To achieve that would require AAV particles bind and stay bound to the imaging surface, which is certainly possible if the surface were functionalized with an affinity ligand or similar ligand to enable capture of the AAV.
Two purified preparations of AAV serotype 5 viral particles were used—one with only empty capsids and one with only full capsids. In both cases, the viral particles were suspended in a PBS buffer (pH 7.4) with 130 mM NaCl and 0.001% (v/v) Pluronic F-188. The virions were purchased from Vigene Biosciences (Maryland, USA). The AAV was purified and separated into empty:full by density ultracentrifugation, then diafiltered into the buffer (PBS+130 mM NaCl with Pluronic F-188). The concentration of full AAV-5 particles was initially 2.95×1013 capsids/ml, and empty capsids were 1.61×1013 capsids/ml. Both the empty and full were then diluted to ˜1×1012 capsids/ml in the PBS+130 mM NaCl buffer.
As shown in
The same AAV-5 preparations as in Example 1 were mixed to give i) an empty-to-full capsid ratio of 1:1 and ii) a ratio of 2:1. The results as shown in
Two AAV-5 preparations were used—one in the PBS, 130 mM NaCl, 0.001% Pluronic F-188 buffer and one in a Tris buffer pH 8.5 with no salt added. Two replicate samples were analyzed for each preparation. The results are shown in
The same AAV-5 preparation as in Example 1 was diluted 1000 times with the buffer (i.e. to a final concentration of ˜1×109 capsids/mL) and analyzed in the microscope. As shown in
This written description uses examples to disclose the invention, including the best mode, and also to enable any person skilled in the art to practice the invention, including making and using any devices or systems and performing any incorporated methods. The patentable scope of the invention is defined by the claims, and may include other examples that occur to those skilled in the art. Such other examples are intended to be within the scope of the claims if they have structural elements that do not differ from the literal language of the claims, or if they include equivalent structural elements with insubstantial differences from the literal languages of the claims. All patents and patent applications mentioned in the text are hereby incorporated by reference in their entireties as if individually incorporated.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2004254.5 | Mar 2020 | GB | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2021/057103 | 3/19/2021 | WO |
