Patent Grant
11600481
The Sequence Listing submitted Oct. 26, 2020, as a text file named “2020-10-26_Sequence_Listing_WVU-00017-U-US-01_ST25.K” created on Oct. 26, 2020, and having a size of 14,600 bytes is hereby incorporated by reference pursuant to 37 C.F.R. § 1.52(e)(5).
Mass spectrometry is one of the most information-rich analytical techniques for characterizing a broad range of samples. The past decade witnessed explosive growth in development of direct analysis and field portable mass spectrometers with the goal of bringing the analytical capability of mass spectrometry to various field applications including environmental monitoring, pharmaceutical analysis, point of care diagnosis, detection of chemical and/or biological warfare agents, forensic investigation, and discovery and research. A key component for portable mass spectrometers is an ionization source that can directly ionize the sample with minimum sample preparation and/or pretreatment. To date, numerous ambient ionization methods that allow direct sample ionization under atmospheric conditions have been reported. However, most of the existing ambient ionization methods, including desorption electrospray ionization (DESI), easy ambient sonic spray ionization (EASI), plasma-assisted desorption ionization (PADI), and direct analysis in real time (DART) require dedicated and specialized instrumentation or auxiliary gas and solvents, making them less favorable options for many field-portable mass spectrometry applications. Furthermore, complex sample preparation and pretreatment is often required. Currently, the most compelling ionization sources for portable mass spectrometers is paper spray ionization (PSI) or solid substrate based electrospray ionization (ESI) due to their simplicity, minimal sample preparation requirements, and wide range of suitable target molecules. These techniques have been utilized in many applications including biofluid analysis, food sample analysis, and chemical reaction monitoring.
A major limitation of several state-of-the-art ionization methods is the requirement of a high voltage (2-5 kV) to induce electrospray, which increases the external equipment demand for portable applications and incurs safety concerns regarding both operators and living organisms as analytical samples. Although low-voltage and zero-voltage PSI methods have been reported by binding carbon nanotubes to a paper substrate and using pneumatic forces to induce spray, respectively, these methods are achieved at the expense of higher cost, more stringent equipment requirements, and a more limited operational environment.
A further barrier to mass spectrometry analysis is that complex mixtures must be simplified by coupling a separation technique such as gas chromatography, liquid chromatography, or capillary electrophoresis (CE) to the mass spectrometer.
ESI is the most common coupling method for mass spectrometry and liquid chromatography but is difficult to integrate with capillary electrophoresis because both ESI and capillary electrophoresis are voltage-driven techniques. In addition, the low flow rate of capillary electrophoresis is difficult to interface with electrospray ionization. Currently, when capillary electrophoresis and mass spectrometry are coupled, the current limitations of each system interfere with the separation and ionization of complex mixtures. The main strategies to decouple capillary electrophoresis from electrospray are through electrical decoupling with a path to ground, for example, by creating a porous region in the silica capillary and by using a sheath flow.
The use of porous silica to decouple the ESI and capillary electrophoresis voltage is created to allow ions to pass through pores to complete an electrical circuit but to prevent larger molecules from passing through the pores. The porous silica decoupler requires means such as chemical etching with hydrofluoric acid with is difficult to make. Moreover, the porous silica can be considered fragile and can become blocked by the molecules introduced or used in the capillary electrophoresis separation. When voltage is grounded through the porous silica it can crack in the presence of the separation current, even currents exceeding a few μA or following mechanical stress. When the porous silica cracks, molecules and fluid flow pass through the crack and are thus diverted away from the mass spectrometer. This is particularly problematic because high voltage is sometimes required for efficient separations. Electrokinetic injection is a preferred injection method for capillary electrophoresis because it produces smaller analyte bands; however, in this method, analyte is driven with voltage rather than pressure, making the technique incompatible with use of the porous silica. One strategy to improve protein separation is to modify the capillary surface, but modified capillaries tend to have limited lifetimes, which in turn shortens the lifetime of the porous silica.
Meanwhile, the sheath flow approach surrounds the separation capillary with a flow of liquid. The voltage is grounded in the sheath flow to decouple the separation voltage and current from the electrospray voltage and current. However, the additional liquid from the sheath flow dilutes the sample, in turn reducing the detector sensitivity and requiring a higher concentration of analyte for detection.
For many analytes, a voltage-free ionization method would be advantageous. These include certain biomolecules as well as chemicals sensitive to electrochemical reactions. To date, several voltage-free ionization methods have been coupled to liquid chromatography (LC) systems including thermospray, sonic spray ionization (SSI), and solvent assisted inlet ionization (SAII). In some instances, ultrasonic agitation has also been used as an effective voltage-free ionization strategy. However, existing mechanical ultrasonic ionization methods are difficult to integrate with LC systems as these methods require a liquid sample to be placed on a substrate surface which is not directly compatible with an LC fluidic system. Although surface acoustic wave nebulization (SAWN) has been coupled to LC by placing the outlet of the LC capillary tubing on top of the SAW substrate for peptide analysis, this coupling strategy is prone to dead volume, carryover, and injection variation effects. As a result, the optimal flow rate range for this configuration is limited to 1-5 μL/min.
Despite advances in portable, field-deployable, and low-voltage ionization methods for mass spectrometry, at a minimum, these techniques still require specialized technical knowledge to use; may require external gases, fluids, or sources of electricity, and are associated with safety issues for operators and living organisms being used as analytical samples. Furthermore, separation techniques such as liquid chromatography and capillary electrophoresis may be required for complex mixtures of analytes; however, current and voltage requirements for ionization and electrophoretic separation may be difficult to integrate or, in some cases, incompatible, and existing methods for decoupling these and/or reducing interference rely on expensive, fragile equipment and/or require high concentrations of sample. What is needed are a zero-voltage, field-deployable ionization method for mass spectrometry that can be coupled to a separation mechanism without the expense, fragility, and high sample concentration requirements that limit implementation of existing technologies. It would further be desirable if the method could overcome the limitations of known discrete connection methods. These needs and other needs are satisfied by the present disclosure.
In accordance with the purpose(s) of the present disclosure, as embodied and broadly described herein, the disclosure, in one aspect, relates to a vibrating sharp edge spray ionization (VSSI) method suitable for coupling with a mass spectrometer, a VSSI method modified with a capillary suitable for use with continuous-flow separation methods such as liquid chromatography, and a VSSI method suitable for coupling with a capillary electrophoresis (CE) device in order to introduce the CE sample flow into a mass spectrometer. Also disclosed herein are devices for carrying out these methods and methods of making the same.
Other systems, methods, features, and advantages of the present disclosure will be or become apparent to one with skill in the art upon examination of the following drawings and detailed description. It is intended that all such additional systems, methods, features, and advantages be included within this description, be within the scope of the present disclosure, and be protected by the accompanying claims. In addition, all optional and preferred features and modifications of the described embodiments are usable in all aspects of the disclosure taught herein. Furthermore, the individual features of the dependent claims, as well as all optional and preferred features and modifications of the described embodiments are combinable and interchangeable with one another.
Many aspects of the present disclosure can be better understood with reference to the following drawings. The components in the drawings are not necessarily to scale, emphasis instead being placed upon clearly illustrating the principles of the present disclosure. Moreover, in the drawings, like reference numerals designate corresponding parts throughout the several views.
Additional advantages of the invention will be set forth in part in the description which follows, and in part will be obvious from the description, or can be learned by practice of the invention. The advantages of the invention will be realized and attained by means of the elements and combinations particularly pointed out in the appended claims. It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory only and are not restrictive of the invention, as claimed.
Many modifications and other embodiments disclosed herein will come to mind to one skilled in the art to which the disclosed compositions and methods pertain having the benefit of the teachings presented in the foregoing descriptions and the associated drawings. Therefore, it is to be understood that the disclosures are not to be limited to the specific embodiments disclosed and that modifications and other embodiments are intended to be included within the scope of the appended claims. The skilled artisan will recognize many variants and adaptations of the aspects described herein. These variants and adaptations are intended to be included in the teachings of this disclosure and to be encompassed by the claims herein.
Although specific terms are employed herein, they are used in a generic and descriptive sense only and not for purposes of limitation.
As will be apparent to those of skill in the art upon reading this disclosure, each of the individual embodiments described and illustrated herein has discrete components and features which may be readily separated from or combined with the features of any of the other several embodiments without departing from the scope or spirit of the present disclosure.
Any recited method can be carried out in the order of events recited or in any other order that is logically possible. That is, unless otherwise expressly stated, it is in no way intended that any method or aspect set forth herein be construed as requiring that its steps be performed in a specific order. Accordingly, where a method claim does not specifically state in the claims or descriptions that the steps are to be limited to a specific order, it is no way intended that an order be inferred, in any respect. This holds for any possible non-express basis for interpretation, including matters of logic with respect to arrangement of steps or operational flow, plain meaning derived from grammatical organization or punctuation, or the number or type of aspects described in the specification.
All publications mentioned herein are incorporated herein by reference to disclose and describe the methods and/or materials in connection with which the publications are cited. The publications discussed herein are provided solely for their disclosure prior to the filing date of the present application. Nothing herein is to be construed as an admission that the present invention is not entitled to antedate such publication by virtue of prior invention. Further, the dates of publication provided herein can be different from the actual publication dates, which can require independent confirmation.
While aspects of the present disclosure can be described and claimed in a particular statutory class, such as the system statutory class, this is for convenience only and one of skill in the art will understand that each aspect of the present disclosure can be described and claimed in any statutory class.
It is also to be understood that the terminology used herein is for the purpose of describing particular aspects only and is not intended to be limiting. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which the disclosed compositions and methods belong. It will be further understood that terms, such as those defined in commonly used dictionaries, should be interpreted as having a meaning that is consistent with their meaning in the context of the specification and relevant art and should not be interpreted in an idealized or overly formal sense unless expressly defined herein.
Prior to describing the various aspects of the present disclosure, the following definitions are provided and should be used unless otherwise indicated. Additional terms may be defined elsewhere in the present disclosure.
As used herein, “comprising” is to be interpreted as specifying the presence of the stated features, integers, steps, or components as referred to, but does not preclude the presence or addition of one or more features, integers, steps, or components, or groups thereof. Moreover, each of the terms “by”, “comprising,” “comprises”, “comprised of,” “including,” “includes,” “included,” “involving,” “involves,” “involved,” and “such as” are used in their open, non-limiting sense and may be used interchangeably. Further, the term “comprising” is intended to include examples and aspects encompassed by the terms “consisting essentially of” and “consisting of.” Similarly, the term “consisting essentially of” is intended to include examples encompassed by the term “consisting of.
As used in the specification and the appended claims, the singular forms “a,” “an” and “the” include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to “a mobile phase” or “an analyte,” including, but not limited to, combinations of two or more such mobile phases, analytes, and the like.
It should be noted that ratios, concentrations, amounts, and other numerical data can be expressed herein in a range format. It will be further understood that the endpoints of each of the ranges are significant both in relation to the other endpoint, and independently of the other endpoint. It is also understood that there are a number of values disclosed herein, and that each value is also herein disclosed as “about” that particular value in addition to the value itself. For example, if the value “10” is disclosed, then “about 10” is also disclosed. Ranges can be expressed herein as from “about” one particular value, and/or to “about” another particular value. Similarly, when values are expressed as approximations, by use of the antecedent “about,” it will be understood that the particular value forms a further aspect. For example, if the value “about 10” is disclosed, then “10” is also disclosed.
When a range is expressed, a further aspect includes from the one particular value and/or to the other particular value. For example, where the stated range includes one or both of the limits, ranges excluding either or both of those included limits are also included in the disclosure, e.g. the phrase “x to y” includes the range from ‘x’ to ‘y’ as well as the range greater than ‘x’ and less than ‘y’. The range can also be expressed as an upper limit, e.g. ‘about x, y, z, or less’ and should be interpreted to include the specific ranges of ‘about x’, ‘about y’, and ‘about z’ as well as the ranges of ‘less than x’, less than y′, and ‘less than z’. Likewise, the phrase ‘about x, y, z, or greater’ should be interpreted to include the specific ranges of ‘about x’, ‘about y’, and ‘about z’ as well as the ranges of ‘greater than x’, greater than y′, and ‘greater than z’. In addition, the phrase “about ‘x’ to ‘y’”, where ‘x’ and ‘y’ are numerical values, includes “about ‘x’ to about ‘y’”.
It is to be understood that such a range format is used for convenience and brevity, and thus, should be interpreted in a flexible manner to include not only the numerical values explicitly recited as the limits of the range, but also to include all the individual numerical values or sub-ranges encompassed within that range as if each numerical value and sub-range is explicitly recited. To illustrate, a numerical range of “about 0.1% to 5%” should be interpreted to include not only the explicitly recited values of about 0.1% to about 5%, but also include individual values (e.g., about 1%, about 2%, about 3%, and about 4%) and the sub-ranges (e.g., about 0.5% to about 1.1%; about 5% to about 2.4%; about 0.5% to about 3.2%, and about 0.5% to about 4.4%, and other possible sub-ranges) within the indicated range.
As used herein, the terms “about,” “approximate,” “at or about,” and “substantially” mean that the amount or value in question can be the exact value or a value that provides equivalent results or effects as recited in the claims or taught herein. That is, it is understood that amounts, sizes, formulations, parameters, and other quantities and characteristics are not and need not be exact, but may be approximate and/or larger or smaller, as desired, reflecting tolerances, conversion factors, rounding off, measurement error and the like, and other factors known to those of skill in the art such that equivalent results or effects are obtained. In some circumstances, the value that provides equivalent results or effects cannot be reasonably determined. In such cases, it is generally understood, as used herein, that “about” and “at or about” mean the nominal value indicated ±10% variation unless otherwise indicated or inferred. In general, an amount, size, formulation, parameter or other quantity or characteristic is “about,” “approximate,” or “at or about” whether or not expressly stated to be such. It is understood that where “about,” “approximate,” or “at or about” is used before a quantitative value, the parameter also includes the specific quantitative value itself, unless specifically stated otherwise.
As used herein, the terms “optional” or “optionally” means that the subsequently described event or circumstance can or cannot occur, and that the description includes instances where said event or circumstance occurs and instances where it does not.
As used herein, “voltage-free,” “voltage-free zone,” “voltage-free environment,” and similar terms refer to the absence of high voltage fields (e.g., on the order of kV per cm) typically used to ionize samples for mass spectrometers. In one aspect, the electrical signal used to drive the vibration generator (an electromechanical transducer or a piezoelectric transducer in some embodiments) is on the order of volts to tens of volts, “peak-to-peak,” and is considered part of the voltage-free zone or voltage-free environment as defined herein, since that electrical signal is not used to directly create ions through its field strength alone.
A “piezoelectric” material is a material that produces an electric charge when subjected to mechanical stress. Piezoelectric materials include, but are not limited to, potassium sodium tartrate tetrahydrate (also known as Rochelle salt), quartz, cane sugar, topaz, tourmaline, apatite, bone (primarily due to apatite crystals), barium titanate, lead zirconate titanate, and combinations thereof. In one aspect, the electric charge is proportional to the mechanical stress that is applied to the material. Meanwhile, a “piezoelectric transducer” converts electrical charges produced by piezoelectric materials into energy.
A “resonant frequency” is a natural frequency of vibration for a physical object that is vibrating. The resonant frequency is determined by the properties of the object. Most objects possess multiple resonant frequencies. When an object is subjected to a complex excitation, that object will vibrate at its own resonant frequencies.
Unless otherwise specified, temperatures referred to herein are based on atmospheric pressure (i.e. one atmosphere).
Vibrating Sharp-Edge Enabled Aerosol Generator
In one aspect, disclosed herein is a vibrating sharp-edge enabled aerosol generator. In a further aspect, the disclosed vibrating sharp-edge enabled aerosol generator can be utilized to controllably provide a sample in droplet form. For example, the disclosed vibrating sharp-edge enabled aerosol generator can be utilized to generate droplets for an ionization source of mass spectrometer, and accordingly, utilized in methods for mass spectrometry that can directly ionize samples with minimum preparation and/or pretreatment. In a further aspect, the method is voltage-free. In another aspect, the source is constructed only of two components.
In a further aspect, the disclosed vibrating sharp-edge enabled aerosol generator can be used to controllably generate droplets having an average diameter of about 1 μm, 2 μm, 3 μm, 4 μm, 5 μm, 6 μm, 7 μm, 8 μm, 9 μm, 10 μm, 11 μm, 12 μm, 13 μm, 14 μm, 15 μm, 16 μm, 17 μm, 18 μm, 19 μm, 20 μm, 21 μm, 22 μm, 23 μm, 24 μm, 25 μm, 26 μm, 27 μm, 28 μm, 29 μm, 30 μm; or any range encompassed by a lower and upper limit utilizing any two of the foregoing values; or any set of the foregoing values.
In a further aspect, a plurality of the disclosed vibrating sharp-edge enabled aerosol generator can be utilized together, each independently providing droplets to an ionization source of a mass spectrometer. In various further aspects, the vibrating sharp-edge enabled aerosol generator can be utilized, e.g., a single vibrating sharp-edge enabled aerosol generator or a plurality of vibrating sharp-edge enabled aerosol generators, to provide droplets to an input, e.g., as an input to other analytical instruments or for carrying out in droplet reactions.
In some aspects, the droplets are generated as droplets in air. In other aspects, the droplets can be generated as droplets within a two-phase liquid system, i.e., water droplets generated into a surrounding oil medium.
In one aspect, the first component is a thin, rigid substrate. In a further aspect, the thin, rigid substrate is made from glass, quartz, silicon, silicon wafer, brass, steel, hard plastic, a ceramic material, metal, a composite material, fused silica, or a combination thereof. In one aspect, the substrate can be polyether ether ketone (PEEK), pyrolytic boron nitride (PBN), or another material that is less fragile than glass. In a further aspect, a sturdier substrate is preferred over glass for field operations due to the decreased likelihood of breakage. Further in this aspect, the thin, rigid substrate can be a commercial object such as, for example, a glass microscope slide. In one aspect, the thin, rigid substrate includes a proximal end with a flat surface and a distal end with at least one sharp edge. In another aspect, the sharp edge is a corner of the thin, rigid substrate. In one aspect, any hard material that does not cause damping of vibration can serve as the thin, rigid substrate.
In one aspect, the surface of the thin, rigid substrate can be chemically modified with, for example, a polymethylsiloxane or other silicone-based network in order to increase hydrophobicity. In a further aspect, using a more hydrophobic surface may further decrease needed flow rate and/or generate smaller droplets at the sharp edge.
In another aspect, the working dimension and thickness of the substrate can vary. In one aspect, different dimensions of substrate can be used (i.e., 24×50 mm, 24×60 mm, 24×75 mm, etc.). In another aspect, different thicknesses of substrate can be used, such as a No. 0, No. 1, or No. 1.5 microscope slide (0.08-0.13 mm, 0.13-0.16 mm, and 0.16-0.19 mm, respectively). In one aspect, a thinner substrate corresponds to a lower requirement for input power. In another aspect, the substrate can have an irregular shape such as, for example, a triangle. Further in this aspect, the irregular shape can be a capillary with a tapered tip. In still another aspect, the substrate can have microchannels to direct fluid flow.
In a further aspect, the substrate can have a thickness of about 0.01 mm, 0.02 mm, 0.03 mm, 0.04 mm, 0.05 mm, 0.06 mm, 0.07 mm, 0.08 mm, 0.09 mm, 0.10 mm, 0.11 mm, 0.12 mm, 0.13 mm, 0.14 mm, 0.15 mm, 0.16 mm, 0.17 mm, 0.18 mm, 0.19 mm, 0.20 mm, 0.21 mm, 0.22 mm, 0.23 mm, 0.24 mm, 0.25 mm, 0.26 mm, 0.27 mm, 0.28 mm, 0.29 mm, 0.30 mm, 0.31 mm, 0.32 mm, 0.33 mm, 0.34 mm, 0.35 mm, 0.36 mm, 0.37 mm, 0.38 mm, 0.39 mm, 0.40 mm, 0.41 mm, 0.42 mm, 0.43 mm, 0.44 mm, 0.45 mm, 0.46 mm, 0.47 mm, 0.48 mm, 0.49 mm, 0.50 mm, 0.51 mm, 0.52 mm, 0.53 mm, 0.54 mm, 0.55 mm, 0.56 mm, 0.57 mm, 0.58 mm, 0.59 mm, 0.60 mm, 0.61 mm, 0.62 mm, 0.63 mm, 0.64 mm, 0.65 mm, 0.66 mm, 0.67 mm, 0.68 mm, 0.69 mm, 0.70 mm, 0.71 mm, 0.72 mm, 0.73 mm, 0.74 mm, 0.75 mm, 0.76 mm, 0.77 mm, 0.78 mm, 0.79 mm, 0.80 mm, 0.81 mm, 0.82 mm, 0.83 mm, 0.84 mm, 0.85 mm, 0.86 mm, 0.87 mm, 0.88 mm, 0.89 mm, 0.90 mm, 0.91 mm, 0.92 mm, 0.93 mm, 0.94 mm, 0.95 mm, 0.96 mm, 0.97 mm, 0.98 mm, 0.99 mm, 1.00 mm, 1.01 mm, 1.02 mm, 1.03 mm, 1.04 mm, 1.05 mm, 1.06 mm, 1.07 mm, 1.08 mm, 1.09 mm, 1.10 mm, 1.11 mm, 1.12 mm, 1.13 mm, 1.14 mm, 1.15 mm, 1.16 mm, 1.17 mm, 1.18 mm, 1.19 mm, 1.20 mm, 1.21 mm, 1.22 mm, 1.23 mm, 1.24 mm, 1.25 mm, 1.26 mm, 1.27 mm, 1.28 mm, 1.29 mm, 1.30 mm, 1.31 mm, 1.32 mm, 1.33 mm, 1.34 mm, 1.35 mm, 1.36 mm, 1.37 mm, 1.38 mm, 1.39 mm, 1.40 mm, 1.41 mm, 1.42 mm, 1.43 mm, 1.44 mm, 1.45 mm, 1.46 mm, 1.47 mm, 1.48 mm, 1.49 mm, 1.50 mm, 1.51 mm, 1.52 mm, 1.53 mm, 1.54 mm, 1.55 mm, 1.56 mm, 1.57 mm, 1.58 mm, 1.59 mm, 1.60 mm, 1.61 mm, 1.62 mm, 1.63 mm, 1.64 mm, 1.65 mm, 1.66 mm, 1.67 mm, 1.68 mm, 1.69 mm, 1.70 mm, 1.71 mm, 1.72 mm, 1.73 mm, 1.74 mm, 1.75 mm, 1.76 mm, 1.77 mm, 1.78 mm, 1.79 mm, 1.80 mm, 1.81 mm, 1.82 mm, 1.83 mm, 1.84 mm, 1.85 mm, 1.86 mm, 1.87 mm, 1.88 mm, 1.89 mm, 1.90 mm, 1.91 mm, 1.92 mm, 1.93 mm, 1.94 mm, 1.95 mm, 1.96 mm, 1.97 mm, 1.98 mm, 1.99 mm, 2.00 mm; or any range encompassed by a lower and upper limit utilizing any two of the foregoing values; or any set of the foregoing values.
In one aspect, the second component is a vibration generator. In a further aspect, the vibration generator is fixed to the flat surface at the proximal end of the thin, rigid substrate in order to vibrate the sharp edge of the distal end of the thin, rigid substrate. In a still further aspect, the vibration generator is an electromechanical transducer such as, for example, a piezoelectric transducer. In one aspect, activation of the vibration generator causes the sharp edge of the thin, rigid substrate to vibrate. In a further aspect, vibration of the combined body of the vibration generator and thin, rigid substrate occurs at the resonant frequency of the combined body.
In another aspect, the vibrating sharp edge nebulizes a portion of a liquid sample into a spray of droplets upon physical contact between the vibrating sharp edge and the liquid sample. In a further aspect, the droplets ionize in a voltage-free zone prior to entering a mass spectrometer connected to the aerosol generator disclosed herein. In an alternative aspect, ionization occurs when a voltage is applied to the vibration generator. In one aspect, the spray of droplets are in aerosol form (i.e., water in air). In an alternative aspect, VSSI can be used to generate liquid droplets in another immiscible liquid, such as, for example, a water in oil emulsion (
In various aspects, the liquid can be delivered via a capillary to the vibrating sharp of the substrate. The capillary can be prepared from a glass material or a conductive material, e.g., stainless steel.
In one aspect, disclosed herein is an apparatus for producing a spray of liquid droplets. In a further aspect, the apparatus includes a thin, rigid substrate bounded by a sharp edge and having a flat surface, a vibration generator fixed to the flat surface, wherein the vibration generator vibrates the sharp edge. Further in this aspect, a portion of the vibrating sharp edge is used to contact a liquid sample. In one aspect, when the vibrating sharp edge contacts the liquid sample, a portion of the liquid sample is aerosolized. In a further aspect, when the vibrating sharp edge contacts the liquid sample, the vibrating sharp edge ionizes a portion of the liquid sample. In one aspect, ionization occurs in a voltage-free zone. In still another aspect, the apparatus is connected to a mass spectrometer for the purpose of mass spectral analysis of the aerosolized and ionized liquid sample.
In one aspect, the voltage-free ionization method disclosed herein is referred to as Vibrating Sharp-edge Spray Ionization (VSSI). In one aspect, VSSI is simpler and more flexible than other voltage-free ionization methods such as, for example, sonic spray, ultrasonic nebulization, and solvent-assisted inlet ionization (SAII). In another aspect, VSSI enables in situ analysis through direct, contact-based ionization, without the need for extensive and/or complicated sample preparation techniques. Further in this aspect, trace chemicals on wet human and/or animal skin, as well as other substrates and surfaces, can be ionized using VSSI. In one aspect, other methods of ionization (for example, ESI) cannot be used in this matter due to safety concerns relating to high voltage. In still another aspect, samples aerosolized and ionized by VSSI can be analyzed in both positive and negative ion modes in a connected mass spectrometer. In a still further aspect, two VSSI sources can be simultaneously operated in order to study chemical reactions, in-source protein denaturation, solution phase hydrogen-deuterium exchange, and other phenomena as they occur in droplets. In one aspect, VSSI is advantageous over ESI in this regard, as the zero-voltage characteristics of VSSI allow multiple sources to be operated in close proximity whereas, with ESI, electrical breakdown (when opposite polarity needles are used) and/or droplet repulsion (when similar polarity needles are used) can occur.
In one aspect, the VSSI source can be operated by placing a drop of sample to be nebulized directly on the thin, rigid substrate. In an alternative aspect, the VSSI source can be operated by contacting a sample on a substrate with the edge of the thin, rigid substrate. In some aspects, this second mode of operation is useful in aerosolizing small amounts of fluid that are otherwise difficult to retrieve using common laboratory techniques, or, alternatively, to probe local chemical information with a solid glass tip.
In one aspect, VSSI is superior to conventional acoustic nebulization because conventional acoustic nebulization generates droplets from the entire liquid-gas interface, which may lead to the loss of droplets at the mass spectrometer inlet, thereby resulting in reduced sensitivity. In another aspect, VSSI is advantageous in that, in conventional acoustic nebulization, liquid droplets must be placed on top of a piezoelectric substrate, while in VSSI, the thin, rigid substrate merely needs to contact the liquid sample. In still another aspect, VSSI is advantageous in that an inexpensive piezoelectric transducer and glass microscope slide (together, under $1) are sufficient to cause nebulization in VSSI. In still another aspect, the exposed thin, rigid substrate (e.g., glass microscope slide) can be cleaned and reused. In one aspect, the transducer and substrate can be bonded using hard glue such as, for example superglue, UV- or thermal-curable gel, and the like.
In another aspect, the working frequency of VSSI depends on the material, dimensions, and geometry of the substrate and can be from about 4 to about 120 kHz, or can be about 4, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 110, or about 120 kHz, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In a further aspect, the applied waveform can be a sine wave, a square wave, or a modulated wave.
In one aspect, the peak-to-peak voltage required for VSSI is from about 10 to about 50 V, or is about 10, 15, 20, 25, 30, 35, 40, 45, or about 50 V, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values.
In still another aspect, VSSI is able to work directly with non-polar solvents, which is not possible with ESI-based ionization methods. In one aspect, VSSI can be used with water, toluene, hexane, acetonitrile, a fluorocarbon oil such as FLUORINERT™ FC-40, a coated silica colloid such as PERCOLL® solution (trade name of a product from GE Healthcare Bio-Sciences), and miscible combinations thereof. In one aspect, any liquid with a viscosity lower than 20 cps is suitable for VSSI. In a further aspect, more viscous fluids require higher input powers to ionize. As an example, FC-40 with a viscosity of 4 cps requires 15 Vpp, whereas PERCOLL® with a viscosity of 15 cps requires a minimum of 35 Vpp for aerosolization.
The exact physical process by which the vibrating sharp edge induces nebulization is still under investigation. Without wishing to be bound by theory, it appears that the high frequency vibration at the edge of the thin, rigid substrate causes the detachment of liquid droplets from the bulk fluid, resulting in a continuous spray of fluid from the thin, rigid substrate. It has been further speculated that relatively high amplitude vibration induces fast streaming velocity, a thin layer of fluid at the edge of the thin, rigid substrate, and localized heat, all of which are thought, in some aspects, to contribute to liquid aerosolization.
In one aspect, a well-defined droplet on the surface being analyzed is not necessary for direct VSSI. In some aspects, a thin layer of liquid film is sufficient to generate liquid spray. In a further aspect, this could be useful in field applications such as, for example, an operating room, in order to help surgeons probe the chemical makeup of tissue around a pathological site. In one aspect, VSSI nebulization can safely and effectively be conducted on a variety of wet surfaces and substrates including, but not limited to, cardboard; human or animal skin, hair, feathers, or organs; items suspected of containing explosives or illegal drugs; paper currency; crop plants; building materials; pharmaceutical and/or supplement tablets, pills, capsules, and the like; food or cosmetic items or packaging; cooking surfaces; postal mail; packages delivered by courier services; crime scene surfaces; surfaces at the scenes of suspected terror attacks; environmental surfaces being assessed for pollution or contamination; and any other surface useful in a law enforcement, military, medical, veterinary, environmental, food preparation, manufacturing quality control, pharmaceutical, metabolomics, proteomics, agricultural, or related application or endeavor.
In one aspect, VSSI can be used by the military, law enforcement, first responders, and government agencies for performing environmental assessments, detection of chemical threats, and similar applications. In a further aspect, VSSI ionization techniques can be harnessed for alternative applications including, but not limited to, drug delivery, in-droplet chemical synthesis, cooling, material fabrication, and the like.
Use of mass spectrometry in the operating room has recently gained attention due to the potential of this technique to provide information about the chemical makeup of tissues in and near the surgical incision and/or location of the operation. For example, iKnife technology uses rapid evaporative ionization mass spectrometry (REIMS) to characterize cells in regions of surgical incision. However, REIMS is limited in that information can only be obtained in the region of the incision, and further, REIMS requires destructive methods for generating droplets for ion generation. Furthermore, REIMS requires peripheral technology such as an ESI source that increases device cost, expertise required for operation, and bulkiness of instrumentation. In one aspect, VSSI overcomes these limitations of REIMS by being biocompatible and thus able to contact tissue directly. In a further aspect, a VSSI source has a small footprint and can be operated with a minimal amount of training. In a still further aspect, VSSI can be employed to analyze not only surgical boundaries but can also be used to collect information across the entire surgical region.
In another aspect, VSSI can be employed to determine the identity of an infectious agent afflicting an individual. Traditionally, matrix-assisted laser desorption ionization (MALDI) has been used to search for chemical signatures of different bacteria. In one aspect, VSSI is preferable to MALDI due to lower cost. In a further aspect, VSSI is useful for drug discovery and the screening of drug candidates. In one aspect, VSSI may be useful for rapid initial screening and may be useful in determining binding affinity to specific targets (e.g., through use of two VSSI sources or by another method). In an alternative aspect, VSSI can be used to assess protein stability and denaturation; exemplary procedures for performing protein denaturation experiments using parallel VSSI sources are discussed in the Examples.
In another aspect, because VSSI relies on a thin, rigid substrate such as, for example, a glass microscope slide, it is relatively simple to automate slide washing and thus repeated sampling of the same or different sample liquids, thereby increasing experimental throughput. In an alternative aspect, since microscope slides and other inexpensive substrates are employed, these can easily be switched out to prevent sample carryover.
In another aspect, VSSI can be used as a direct replacement for ESI and similar ionization methods, including DESI, PSI, and the like, in nearly any application. In one aspect, VSSI can be used in MS imaging. In a further aspect, VSSI is advantageous compared to DESI because it has higher resolution. In one aspect, resolution is dictated by the sharp edge used in ionization, whereas DESI produces a wide electrospray plume that is rastered across the sample. By rastering the sharp edge, instead, in one aspect, VSSI can provide a much clearer picture of the locations of different chemical compounds. In a further aspect, VSSI is non-destructive, enabling multiple imaging passes to provide a more robust assessment. In one aspect, this property is expected to be especially useful for biomarker discovery.
In another aspect, vibration can be induced by applying an RF signal to the piezoelectric transducer with a frequency equal to or a frequency combination encompassing the natural or resonance frequency of the VSSI source. In a further aspect, energy for aerosolization is provided by the vibration resonance of the thin, rigid substrate when exposed to the piezoelectric transducer vibrating at its natural frequency. In one aspect, when the solvent is water, with a Vpp of from about 12.7 to about 30.6 V, droplet spray is generated only from liquid touching the vibrating edge of the thin, rigid substrate. In another aspect, with a Vpp of greater than 32.0 V, aerosolization occurs across the entirety of the liquid-gas interface. In still another aspect, no aerosolization occurs when a water droplet is placed near, but not touching, the edge of the thin, rigid substrate. In any of these aspects, lower power inputs are required for VSSI to achieve nebulization.
In one aspect, droplet size in VSSI can be tuned based on solvent conditions, input voltage, and combinations thereof. In a further aspect, smaller droplets lead to improved ionization efficiency.
In one aspect, when the solvent is water and Vpp is about 12.7 V, average droplet size is about 13 to about 23 μm, or is about 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, or about 23 μm, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In one aspect, the average droplet size under these conditions is about 18±5 μm. In one aspect, when the solvent is water and Vpp is about 19.8 V, average droplet size is about 13 to about 31 μm, or is about 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, or about 31 μm, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In one aspect, the average droplet size under these conditions is about 22±9 μm. In one aspect, when the solvent is water and Vpp is about 26.8 V, average droplet size is about 19 to about 31 μm, or is about 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, or about 31 μm, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In one aspect, the average droplet size under these conditions is about 25±6 μm. In an alternative aspect, when the solvent is a 1:1 mixture of acetonitrile and water with 1% acetic acid (v/v), average droplet size is about 6 to about 14 μm, or is about 6, 7, 8, 9, 10, 11, 12, 13, or about 14 μm, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In one aspect, the average droplet size under these conditions is about 10±4 μm.
In any of the foregoing aspects, average droplet size and thus ionization efficiency can be tuned according to peak-to-peak voltage, solvent composition, and variations and combinations thereof.
In one aspect, due to the presence of a sharp edge on the substrate, with VSSI it is possible to form directional streams of droplets, which is not possible with other nebulization techniques. In a further aspect, this directionality can lead to higher sensitivity as droplets can be directed to the inlet region of a mass spectrometer. In a still further aspect, the sharp edge of the substrate in conjunction with the surface tension of the solvent being used can draw liquid to the sharp edge; in this aspect, liquid pumping is not required, thus reducing instrumentation requirements even further.
In one aspect, VSSI may be useful in probing the conformation or folding of biomolecules. In a further aspect, multiple sources can be used to denature or renature proteins within droplets, or can be used to be study the formation of protein complexes.
In still another aspect, VSSI can be useful to monitor rapid chemical reactions, including elucidating the kinetics of rapid reactions. In one aspect, VSSI can be used to monitor enzyme kinetics. Further in this aspect, an enzyme of interest would be deployed on one source and the substrate on a second source. The reactants and products could then be monitored by mass spectrometry after VSSI ionization. Still further in this aspect, a knowledge of droplet size could provide information about the lifetime of the droplet and thus information about reaction kinetics. In a parallel aspect, a similar technique could be used to monitor non-enzymatic reactions by depositing different reactants on different sources.
In one aspect, VSSI can be used as a source for any type of mass spectrometry analysis or related technique such as, for example, ion mobility spectrometry, tandem mass spectrometry, ion mobility mass spectrometry, time of flight mass spectrometry, and the like, and can be coupled to a variety of separation methods useful for analyzing complex samples including, but not limited to, liquid chromatography, gas chromatography, and capillary electrophoresis, as well as two dimensional and hybrid methods encompassing any of the above.
Further in this aspect, provided herein are a method and apparatus for integrating a VSSI source with a liquid dispenser and vacuum port for a mass spectrometer (
In a further aspect, the piezoelectric jetting unit deposits an extraction microdroplet onto the target tissue at which time a pre-aligned substrate tip will touch the droplet to generate aerosols via VSSI. Further in this aspect, the aerosols are transported to the vacuum line to the mass spectrometer. In an additional aspect, a piezoelectric position controller can map molecular information relating to the tissue with sub-millimeter resolution. In all of the above aspects, the system is biocompatible and can, for example, allow real-time diagnosis on the operating table or in other time-critical applications.
In one aspect, the apparatus includes an ion funnel chamber to direct analytes into the mass spectrometer. In one aspect, the ion funnel can be constructed from printed circuit board, providing free space between lenses. In a further aspect, the free space can be used to pump away neutral solvent molecules. In a further aspect, the apparatus includes one or more pumping ports configured for attachment to mechanical pumps. In a still further aspect, the mechanical pumps can remove extra solvent molecules.
Capillary Vibrating Sharp-Edge Spray Ionization for Mass Spectrometry Detection
As discussed previously, VSSI offers a convenient way of ionizing target molecules for direct MS analysis. One disadvantage of the thin, rigid substrate platform in VSSI is the difficulty of continuous flow injection analysis. Thus, VSSI may not be suitable for direct coupling with LC or other continuous flow-based MS analyses. In one aspect, provided herein is a modified VSSI method (cVSSI) that can nebulize liquid samples directly at the outlet of a fused silica capillary, which allows for continuous flow-based injection.
In one aspect, a cVSSI instrument includes a capillary attached to a thin, rigid substrate that can be vibrated by a piezoelectric transducer (
In one aspect, described herein is a novel method for direct fluid nebulization from the outlet of a capillary without the need for a nebulization gas or electric field.
In one aspect, positioning of the capillary on the VSSI slide can be critical to nebulization performance. In a further aspect, a short fused silica capillary is positioned on the distal end of a VSSI substrate (see
In one aspect, the capillary is affixed to the VSSI substrate using epoxy, superglue, UV- or heat-curable gel, or any suitable adhesive. In one aspect, the capillary is affixed to the VSSI substrate using a two-part epoxy that cures in approximately one minute.
In one aspect, the sizes of the droplets generated by cVSSI are similar to those generated by VSSI. In one aspect, the average size of droplet generated by cVSSI is from about 7 to about 17 μm, or is about 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, or about 17 μm, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In one aspect, the average size of droplet generated by cVSSI is 12±5 μm.
In one aspect, a capillary with an inner diameter (ID) ranging from about 50 to about 250 μm is suitable for use in cVSSI analysis. In another aspect, the capillary can have a diameter of about 50, about 75, about 100, about 125, about 150, about 175, about 200, about 225, about 250 μm, a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In still another aspect, the capillary has a diameter of 100 μm. In another aspect, as the ID of the capillary decreases, a higher power input to nebulize the liquid sample is required. Without wishing to be bound by theory, as the ID decreases, the thickness of the capillary wall increases, resulting in less efficient vibration at the capillary tip, thus requiring a higher power input.
In a further aspect, the flow rate through the capillary can be about 1 μL/min to 1 mL/min (1000 μL/min) fora 100 μm ID capillary, or can be about 1, about 20, about 50, about 100, about 150, about 200, about 250, about 300, about 350, about 400, about 450, about 500, about 550, about 600, about 650, about 700, about 750, about 800, about 850, about 900, about 950, about 1000 μL/min, a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In a further aspect, the flow rate is 1 μL/min. In another aspect, the flow rate is 20 μL/min. In a still further aspect, the flow rate is 1 mL/min. In another aspect, higher flow rates can be achieved with higher ID capillaries. In one aspect, for a 250 μm capillary, the flow rate through the capillary can be up to about 3 mL/min, or can be about 2.8 mL/min. In a further aspect, fora capillary with an ID less than 100 μm, flow rates less than 1 μL/min can be achieved.
In another aspect, as the flow rate increases, the power requirement for nebulization increases. In one aspect, the power requirement for nebulization is from about 100 mW to about 1 W (1000 mW), or is about 100, 150, 200, 250, 300, 350, 400, 450, 500, 550, 600, 650, 700, 750, 800, 850, 900, 950, about 1000 mW, a combination of any of the foregoing values, or a range encompassing any of the foregoing values fora 100 μm ID capillary. In one aspect, at 1 μL/min the power requirement for nebulizing fluid is about 130 mW. In another aspect, at 20 μL/min, the power requirement for nebulizing fluid is about 260 mW. In still another aspect, at 1 mL/min, the power requirement for nebulizing fluid is about 760 mW.
In another aspect, multiple capillary VSSI sources can be assembled in parallel to achieve simultaneous or sequential sampling and ionization for high throughput screening applications using mass spectrometry. In one aspect, 8 pulled tip cVSSI devices are attached onto a device holder that allows these devices to direct insert into 8 wells of a 96 well plate for direct sampling of liquid samples. After sampling, the devices are positioned close to the inlet of a mass spectrometer for ionization. In one aspect, the operation of multiple VSSI devices are controlled through multi-channel mechanical or solid-state relay.
Capillary Electrophoresis Coupled to VSSI
In one aspect, VSSI sources can be coupled to a separation method such as, for example, capillary electrophoresis. In one aspect, provided herein is an instrument configured to nebulize samples via VSSI that have first been separated by capillary electrophoresis.
In a typical capillary electrophoresis (CE) instrument, after sample introduction, the ends of a fused silica capillary rest in separate electrolyte solutions and voltage is supplied to electrodes in those solutions, which serve as cathode and anode. Depending on the mode of CE and the sample being analyzed, analytes travel from one end of the capillary to the other and are separated based on electrophoretic mobility. In one aspect, presented herein is an interface between a CE system and a mass spectrometer. In a further aspect, the interface uses VSSI as an ionization/nebulization method.
In a further aspect, in the interface disclosed herein, the site of injection is immersed in a vial of background electrolyte as with a typical CE instrument. In a further aspect, however, the detection end of the capillary is designed to be suspended in air while maintaining an electrical connection to the liquid inside of the capillary. In a still further aspect, this can be accomplished by folding a single piece of 25 μm platinum wire into a U shape and positioning this wire directly over or near the orifice of the capillary. In a still further aspect, both ends of the platinum wire can be fixed to the outer surface of the electrophoresis capillary with an adhesive such as, for example, fast-drying epoxy. Further in this aspect, the ends of the platinum wire are then connected to a second wire using a conductive adhesive such as, for example, conductive silver epoxy. In some aspects, the conductive epoxy can be further sealed with another adhesive such as, for example, fast-drying epoxy. Still further in this aspect, the detection end of the capillary can be grounded by connecting this second wire to ground.
In one aspect, the injection end of the capillary can be maintained at positive high voltage to perform normal polarity capillary electrophoresis (i.e., injection at anode and detection at cathode) or can be maintained at negative high voltage to perform reversed polarity capillary electrophoresis (i.e., injection at cathode and detection at anode). In one aspect, in order to avoid introducing gas bubbles into the capillary, the grounded electrode must touch the liquid coming out of the capillary to complete the circuit. Further in this aspect, the grounded electrode should not be placed inside the capillary channel.
In one aspect, the outlet from the electrophoresis capillary is positioned adjacent to a VSSI probe (substrate). In a further aspect, the VSSI probe (i.e., substrate) is a long, thin element such as, for example, a borosilicate capillary that has been pulled to have a narrow tip. In one aspect, in this instance, the VSSI probe tip is from about 5 to about 100 μm in diameter, or is about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, about 100 μm in diameter, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In one aspect, the VSSI probe tip is pulled to about 50 μm in diameter. In another aspect, the VSSI probe tip is positioned at an angle relative to the capillary outlet tip. In one aspect, the angle is from about 70 to about 110°, or is about 70, 75, 80, 85, 90, 95, 100, 105, or about 110°, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In one aspect, the angle is 90°.
In a further aspect, the VSSI probe can touch the capillary surface in order for nebulization to occur. In a still further aspect, the VSSI probe functions optimally when the VSSI probe tip is near the capillary outlet orifice. In one aspect, once the capillary and VSSI probe are assembled as described above, a waveform can be applied to the probe to induce nebulization. In a further aspect, the waveform can range in frequency from about 3 kHz to about 1 MHz (1000 kHz), or can be about 3, 50, 100, 150, 200, 250, 300, 350, 400, 450, 500, 550, 600, 650, 700, 750, 800, 850, 900, 950, or about 1000 kHz, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In a still further aspect, the waveform can be a sine wave, a square wave, or another modulated signal. In a still further aspect, the VSSI probe does not damage or modify the capillary. Further in this aspect, the VSSI probe can be used repeatedly.
In one aspect, the VSSI probe can be coupled with any size of electrophoresis capillary. In a further aspect, the electrophoresis capillary can have an inner diameter (ID) of from about 10 to about 110 μm, or can be about 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 105, or about 110 μm, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In one aspect, the electrophoresis capillary has an ID of 50 μm. In another aspect, the electrophoresis capillary has an ID of 100 μm. In a further aspect, the electrophoresis capillary can have any length suitable for capillary electrophoresis. In one aspect, the electrophoresis capillary is about 50 cm long. In an alternative aspect, the electrophoresis capillary is about 60 cm long.
In one aspect, the capillary electrophoresis flow rate can be from about 2 nL/min to about 1000 nL/min (1 μL/min), or can be about 2, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 105, 110, 120, 130, 140, 150, 200, 250, 300, 350, 400, 450, 500, 550, 600, 650, 700, 750, 800, 850, 900, 950, or about 1000 nL/min, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In a further aspect, flow rates of about 2 nL/min can be paired with narrow bore capillaries such as, for example, 10 μm inner diameter electrophoresis capillaries and conditions of low electroosmotic flow, such as with an uncoated electrophoresis capillary with a background electrolyte at pH 4. In another aspect, flow rates of up to 1 μL/min can be achieved with a large bore capillary such as, for example, 100 μm inner diameter, under conditions that generate a high electroosmotic flow, such as with an uncoated capillary with a background electrolyte at pH 12, or, in an alternative aspect, a coated capillary at a pH that generates high flow.
In another aspect, the capillary electrophoresis flow rate can be from about 10 nL/min to about 500 nL/min. In one aspect, a flow rate of about 10 nL/min can be paired with a 25 μL/min capillary under conditions of low electroosmotic flow. In an alternative aspect, a flow rate of about 500 nL/min can be paired with a larger bore capillary such as, for example, one with 100 μm inner diameter under conditions that generate a moderate electroosmotic flow such as using an uncoated capillary with a background electrolyte at pH 8.
In still another aspect, the capillary electrophoresis flow rate can be from about 50 to about 500 nL/min. In one aspect, when the flow rate is about 50 nL/min, a narrow bore capillary is used such as, for example, one with a 50 μm inner diameter, under conditions of low electroosmotic flow. In still another aspect, capillary bore, flow rate, coating, pH, and background electrolyte can be modified based on the analyte of interest using the above parameters as guidelines.
In one aspect, separations performed using the combined VSSI-capillary electrophoresis approach are reproducible in both time and intensity. In another aspect, VSSI-capillary electrophoresis separations are consistent with commercial equipment at pH values near neutral (such as, for example, around pH 6.5). In still another aspect, VSSI-capillary electrophoresis migration time is shorter at pH values below neutral when compared to commercial instruments (such as, for example, at around pH 5). In one aspect, VSSI-capillary electrophoresis can be performed at any pH compatible with the materials used to construct the instrument, or can be performed at about pH 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10, 10.5, 11, 11.5, or about pH 12, or a combination of any of the foregoing values, or a range encompassing any of the foregoing values. In another aspect, VSSI-capillary electrophoresis can be performed from about pH 2 to about pH 10. Further in this aspect, a coating may be required for the electrophoresis capillary at lower pH values. Still further in this aspect, when ionization occurs at pH 10, either positive or negative ion mode can be used for MS ion collection. In another aspect, VSSI-capillary electrophoresis can be performed from about pH 2 to about pH 7. Further in this aspect, the electrophoresis capillary may require an acid-resistance coating from about pH 2 to about pH 4. Still further in this aspect, the volatile buffering agent for capillary electrophoresis can be selected from formic acid, acetic acid, or ammonium acetate. In yet another aspect, VSSI-capillary electrophoresis can be performed from about pH 4 to about pH 7. Further in this aspect, capillary electrophoresis can generate electrically driven bulk flow with no coating. Still further in this aspect, volatile buffering agents would be applicable for ionization including acetic acid or ammonium acetate.
The following listing of exemplary aspects supports and is supported by the disclosure provided herein.
Aspect 1. An apparatus for ionizing a liquid sample, the apparatus comprising: (a) a thin, rigid substrate; and (b) a vibration generator.
Aspect 2. The apparatus of Aspect 1, wherein the thin, rigid substrate comprises glass, quartz, silicon, hard plastic, a ceramic material, metal, a composite material, fused silica, polyether ether ketone (PEEK), pyrolytic boron nitride (PBN), or a combination thereof.
Aspect 3. The apparatus of Aspect 2, wherein the thin, rigid substrate comprises glass.
Aspect 4. The apparatus of any of Aspect 1-Aspect 3, wherein the thin, rigid substrate comprises a proximal end with a flat surface and a distal end with at least one sharp edge.
Aspect 5. The apparatus of Aspect 4, wherein the sharp edge is a corner.
Aspect 6. The apparatus of any of Aspect 1-Aspect 3, wherein the thin, rigid substrate comprises an irregular shape.
Aspect 7. The apparatus of Aspect 6, wherein the irregular shape comprises a triangle or a capillary with a tapered tip.
Aspect 8. The apparatus of any of Aspect 1-Aspect 3, wherein the thin, rigid substrate comprises microchannels to direct fluid flow.
Aspect 9. The apparatus of Aspect 1, wherein the thin, rigid substrate is chemically modified with a polymethylsiloxane or other silicone-based network in order to increase hydrophobicity.
Aspect 10. The apparatus of any of Aspect 1-Aspect 3, wherein the thin, rigid substrate comprises a glass microscope slide.
Aspect 11. The apparatus of any of Aspect 1-Aspect 3 or Aspect 10, wherein the thin, rigid substrate comprises a top surface area of from about 24×50 mm to about 24×75 mm.
Aspect 12. The apparatus of any of Aspect 1-Aspect 3 or Aspect 10, wherein the thin, rigid substrate comprises a thickness of from about 0.08 mm to about 0.19 mm.
Aspect 13. The apparatus of Aspect 1, wherein the vibration generator is an electromechanical transducer.
Aspect 14. The apparatus of Aspect 13, wherein the electromechanical transducer is a piezoelectric transducer.
Aspect 15. The apparatus of Aspect 4, wherein the vibration generator is fixed to the proximal end of the thin, rigid substrate to form a combined body.
Aspect 16. The apparatus of Aspect 15, wherein activation of the vibration generator causes the sharp edge of the thin, rigid substrate to vibrate.
Aspect 17. The apparatus of Aspect 16, wherein the vibration frequency of the combined body is its resonant frequency.
Aspect 18. A method for producing a spray of droplets, the method comprising: (a) causing the sharp edge of the thin, rigid substrate of Aspect 1 to vibrate, generating a vibrating sharp edge; and (b) contacting a liquid sample with the vibrating sharp edge.
Aspect 19. The method of Aspect 18, wherein the spray of droplets comprises an aerosol.
Aspect 20. The method of Aspect 18, wherein the spray of droplets comprises an emulsion.
Aspect 21. The method of Aspect 18, wherein a droplet of the liquid sample is placed on the thin, rigid substrate.
Aspect 22. The method of Aspect 18, wherein the thin, rigid substrate is used to contact a wet surface.
Aspect 23. The method of Aspect 18, wherein contacting the liquid sample with the vibrating sharp edge causes the spray of droplets to ionize.
Aspect 24. The method of Aspect 23, wherein ionization is voltage-free.
Aspect 25. The method of Aspect 24, wherein voltage is applied to the vibration generator to achieve ionization.
Aspect 26. The method of any of Aspect 18-Aspect 25, wherein the spray of droplets is generated only along the vibrating sharp edge.
Aspect 27. The method of Aspect 26, wherein the spray of droplets is generated continuously and ends only when the vibrating sharp edge is removed from the liquid sample or when the liquid sample has been fully ionized.
Aspect 28. The method of Aspect 18, wherein the liquid sample comprises a solvent.
Aspect 29. The method of Aspect 28, wherein the solvent comprises water, toluene, hexane, acetonitrile, a fluorocarbon oil, a coated silica colloid, or a miscible combination thereof.
Aspect 30. The method of Aspect 22, wherein the wet surface comprises cardboard; human or animal skin, hair, feathers, or organs; items suspected of containing explosives or illegal drugs; paper currency; crop plants; building materials; pharmaceutical and/or supplement tablets, pills, or capsules; food items; food packaging; cosmetic items; cosmetic packaging; cooking surfaces; postal mail; packages delivered by courier services; crime scene surfaces; surfaces at the scenes of suspected terror attacks; environmental surfaces being assessed for pollution or contamination; or the like.
Aspect 31. The method of Aspect 18, wherein application of a radio frequency (RF) signal to the thin, rigid substrate induces vibration.
Aspect 32. The method of Aspect 31, wherein the liquid sample is dissolved in water and the peak-to-peak voltage (Vpp) of the RF signal is from about 12.7 V to about 30.6 V.
Aspect 33. The method of Aspect 32, wherein Vpp is 12.7 V and average droplet size in the spray of droplets is about 18±5 μm.
Aspect 34. The method of Aspect 32, wherein Vpp is 19.8 V and average droplet size in the spray of droplets is about 22±9 μm.
Aspect 35. The method of Aspect 32, wherein Vpp is 26.8 V and average droplet size in the spray of droplets is about 25±6 μm.
Aspect 36. The method of Aspect 31, wherein the liquid sample is dissolved in a 1:1 mixture of acetonitrile and water with 1% acetic acid and the average droplet size in the spray of droplets is about 10±4 μm.
Aspect 37. The apparatus of Aspect 1, further comprising a vacuum port for injecting the liquid sample into a mass spectrometer following ionization.
Aspect 38. The apparatus of Aspect 37, wherein the mass spectrometer can analyze the liquid sample in either positive or negative ion mode.
Aspect 39. A method for analyzing a change to a molecule, the method comprising: (a) introducing a first liquid sample to a first apparatus according to Aspect 1 and generating a first spray of droplets; (b) introducing a second liquid sample to a second apparatus according to Aspect 1 and generating a second spray of droplets; (c) allowing the first spray of droplets and the second spray of droplets to contact one another to form a combined spray of droplets; and (d) introducing the combined spray of droplets into a mass spectrometer.
Aspect 40. The method of Aspect 39, wherein the change to a molecule is protein denaturation, the first liquid sample comprises a protein of interest, and the second liquid sample comprises a reactant, solvent, acid, or base that will denature the protein of interest upon contact.
Aspect 41. The method of Aspect 39, wherein the change to a molecule is a chemical reaction, the first liquid sample comprises a first reactant, the second liquid sample comprises a second reactant, and the chemical reaction will occur when the first spray of droplets and the second spray of droplets contact one another.
Aspect 42. The apparatus of Aspect 1, further comprising: (a) a piezoelectric jetting system to apply small liquid droplets on a surface for molecular extraction; and (b) a vacuum line to transport aerosols to a mass spectrometer.
Aspect 43. The apparatus of Aspect 42, further comprising a piezoelectric position controller.
Aspect 44. The apparatus of Aspect 43, wherein the piezoelectric position controller can modulate the position of the thin, rigid substrate such that molecular information about the surface can be mapped.
Aspect 45. The apparatus of Aspect 1 or Aspect 44, wherein the apparatus is biocompatible.
Aspect 46. The apparatus of Aspect 1, wherein the apparatus further comprises a capillary fixed to the thin, rigid substrate.
Aspect 47. The apparatus of Aspect 46, wherein the capillary is glued to the thin, rigid substrate.
Aspect 48. The apparatus of Aspect 46 or Aspect 47, wherein the capillary comprises an inlet end configured to connect to tubing from a source of continuous liquid flow.
Aspect 49. The apparatus of Aspect 48, wherein the inlet end of the capillary extends about 4 cm past the thin, rigid substrate.
Aspect 50. The apparatus of Aspect 46 or Aspect 47, wherein the capillary comprises an outlet end configured to transmit the ionized liquid sample to a mass spectrometer.
Aspect 51. The apparatus of Aspect 50, wherein the outlet end extends about 1 cm past the thin, rigid substrate.
Aspect 52. The apparatus of Aspect 46, wherein the capillary has an inner diameter of from about 50 to about 250 μm.
Aspect 53. The apparatus of Aspect 52, wherein the capillary has an inner diameter of 100 μm.
Aspect 54. An apparatus comprising the capillary of Aspect 48, wherein the source of continuous liquid flow has a flow rate of from about 1 μL/min to about 1 mL/min.
Aspect 55. The apparatus of Aspect 54, wherein the flow rate is 1 μL/min.
Aspect 56. The apparatus of Aspect 54, wherein nebulization requires a power input and the power input is proportional to the flow rate.
Aspect 57. The apparatus of Aspect 56, wherein the power input is from about 100 mW to about 1 W.
Aspect 58. The apparatus of Aspect 56, wherein, for a 100 μm capillary with a 1 μL/min flow rate, the power input is about 130 mW.
Aspect 59. The apparatus of Aspect 56, wherein, for a 100 μm capillary with a 20 μL/min flow rate, the power input is about 260 mW.
Aspect 60. The apparatus of Aspect 56, wherein, for a 100 μm capillary with a 1 mL/min flow rate, the power input is about 760 mW.
Aspect 61. An interface between a capillary electrophoresis apparatus and a mass spectrometer comprising the apparatus of Aspect 1.
Aspect 62. The interface of Aspect 61, wherein the capillary electrophoresis apparatus comprises a capillary with a detection end suspended in air.
Aspect 63. The interface of Aspect 62, wherein the capillary has an inner diameter of from about 50 to about 100 μm.
Aspect 64. The interface of Aspect 62, wherein the detection end comprises a U-shaped platinum wire.
Aspect 65. The interface of Aspect 64, wherein the platinum wire serves as an electrode for capillary electrophoresis separations.
Aspect 66. The interface of Aspect 64, wherein the platinum wire is grounded.
Aspect 67. The interface of Aspect 66 wherein a flow of liquid exits the detection end and the platinum wire is contacted by the flow of liquid, and wherein the platinum wire does not enter the detection end of the capillary.
Aspect 68. The interface of Aspect 62, wherein the capillary electrophoresis apparatus can be operated in normal polarity mode or in reverse polarity mode.
Aspect 69. The interface of Aspect 62, wherein the thin, rigid substrate comprises a borosilicate capillary pulled to a thin diameter.
Aspect 70. The interface of Aspect 69, wherein the borosilicate capillary is oriented at a 90° angle to the detection end of the capillary included in the capillary electrophoresis apparatus.
Aspect 71. The interface of Aspect 70, wherein the borosilicate capillary touches the detection end.
Aspect 72. The interface of any of Aspect 69-Aspect 71 wherein the borosilicate capillary can be used multiple times prior to replacement.
Aspect 73. The interface of any of Aspect 69-Aspect 71, wherein a waveform is applied to the borosilicate capillary to induce ionization.
Aspect 74. The interface of Aspect 73, wherein the waveform comprises a frequency of from about 3 kHz to about 1 MHz.
Aspect 75. The interface of Aspect 73, wherein the waveform comprises a sine wave or a square wave.
From the foregoing, it will be seen that aspects herein are well adapted to attain all the ends and objects hereinabove set forth together with other advantages which are obvious and which are inherent to the structure.
While specific elements and steps are discussed in connection to one another, it is understood that any element and/or steps provided herein is contemplated as being combinable with any other elements and/or steps regardless of explicit provision of the same while still being within the scope provided herein.
It will be understood that certain features and subcombinations are of utility and may be employed without reference to other features and subcombinations. This is contemplated by and is within the scope of the claims.
Since many possible aspects may be made without departing from the scope thereof, it is to be understood that all matter herein set forth or shown in the accompanying drawings and detailed description is to be interpreted as illustrative and not in a limiting sense.
It is also to be understood that the terminology used herein is for the purpose of describing particular aspects only, and is not intended to be limiting. The skilled artisan will recognize many variants and adaptations of the aspects described herein. These variants and adaptations are intended to be included in the teachings of this disclosure and to be encompassed by the claims herein.
Now having described the aspects of the present disclosure, in general, the following Examples describe some additional aspects of the present disclosure. While aspects of the present disclosure are described in connection with the following examples and the corresponding text and figures, there is no intent to limit aspects of the present disclosure to this description. On the contrary, the intent is to cover all alternatives, modifications, and equivalents included within the spirit and scope of the present disclosure.
The following examples are put forth so as to provide those of ordinary skill in the art with a complete disclosure and description of how the compounds, compositions, articles, devices and/or methods claimed herein are made and evaluated, and are intended to be purely exemplary of the disclosure and are not intended to limit the scope of what the inventors regard as their disclosure. Efforts have been made to ensure accuracy with respect to numbers (e.g., amounts, temperature, etc.), but some errors and deviations should be accounted for. Unless indicated otherwise, parts are parts by weight, temperature is in ° C. or is at ambient temperature, and pressure is at or near atmospheric.
A. Construction of VSSI Device and Mass Spectrometer Settings
The VSSI device was made by attaching a piezoelectric transducer (Murata) to one end of a No. 1 glass microscope glass slide (VWR) using superglue. The RF signal was generated using a Tektronix function generator (AFG-1062) connected to an amplifier (Krohn-Hite 7500).
Droplet images for size measurement were taken using an Olympus IX-73 inverted fluorescence microscope and analyzed using Image J software (v1.51s).
All mass spectrometry experiments were carried out using an Orbitrap mass spectrometer (Thermo). For these experiments, the resolving power was set at 7.0×104 for precursor ion analysis. The capillary inlet was maintained at 250° C. Ion chromatograms were collected for varying times (from 1 to 3 min).
B. Generation of Droplet Spray
A typical sample was ionized by adding a drop of liquid to the edge of a vibrating microscope glass slide (
In some experiments, spray was generated simply by touching liquid on a solid surface with a vibrating glass edge. In one aspect, VSSI was used to successfully induce liquid spray from wet cardboard (
C. Droplet Size
Droplet size is important for both ionization efficiency and chemical processes occurring during ion production. Size distribution of VSSI-generated droplets and factors affecting this size distribution were investigated. Droplets were collected using a petri dish placed 20 mm away from the glass slide. A drop of mineral oil was applied immediately after liquid droplets reached the bottom of the petri dish to prevent further evaporation. The diameter of the droplets was obtained by examination under a microscope. For pure water, average droplet diameter was 18 μm with a standard deviation of 5 μm using a 12.7 Vpp power input (
In addition to voltage input, solvent content was also found to play a role in determining VSSI-generated droplet size. Water was replaced with a 1:1 mixture of water and acetonitrile containing 1% acetic acid, the average droplet size decreased from 18±5 μm to 10±4 μm under the same input power conditions (
D. VSSI as Ionization Source for Mass Spectrometry
A series of 1 mM solutions were prepared using homocysteine, sucrose, polyalanine peptides, and ubiquitin in 1:1 water:acetonitrile with 1% acetic acid. For each solution, 20 μL sample was added to the edge of a glass slide and spray was generated by applying a radio frequency signal of 97.1 kHz and 14.4 Vpp to the piezoelectric transducer. Mass spectra were obtained using an Orbitrap analyzer in positive ion mode with a capillary temperature of 250° C.
Mass spectra revealed ESI-type ions produced by VSSI. Upon VSSI of the homocysteine sample, a dominant peak was observed at m/z of ˜136 (
E. Operation of Multiple Sources Simultaneously
The zero-voltage characteristics of VSSI make it convenient to operate multiple sources in close proximity without worrying about electrical breakdown (in the case of opposite polarity needles) or problems of droplet repulsion (in the case of similar polarity needles). In-droplet denaturation of ubiquitin was demonstrated using two VSSI sources. 40 μL of a solution of ubiquitin in water was placed on one source and 40 μL of acetonitrile (containing 1% acetic acid) was placed on a second source. The two sources were positioned near the mass analyzer inlet as shown in
F. Direct Ionization from Living Organisms
The tip of a vibrating glass slide was touched to a wet human finger, generating a liquid spray in situ without the need for sample transfer (
In an alternative experiment, a trace amount of red food coloring on a fingertip was detected by VSSI using the same setup. Red food dye mixture (Wilton Gel Food Color) was diluted 100-fold and a small drop was applied to the fingertip. The liquid was wiped off with a paper towel and a red trace was observed on the fingertip. 5 μL of water was then applied to the red trace and ionized by direct VSSI. A peak having a nominal m/z of 835 was observed in the mass spectrum and corresponds with [M−H]− ions of the red dye (erythrosine) as shown in
A. Materials and Reagents
High performance liquid chromatography (HPLC) grade acetonitrile, water, ammonium acetate, formic acid, methanol, and benzoic acid were purchased from Fisher Scientific (NJ, USA). Sucrose, caffeine, acetaminophen, dopamine, acetic acid, cytochrome c (equine), and pepsin (porcine, 2500 units/mg protein) were purchased from Sigma Aldrich (MO, USA) and used without further purification. Guanine and guanosine were purchased from Acros Organics (NJ, USA). Angiotensin II was purchased from Alfa Aesar (MA, USA). Ubiquitin was purchased from Boston Biochem (MA, USA).
B. Instrumentation
A high performance Q-Exactive (ThermoScientific) mass spectrometer featuring quadrupole precursor selection with high resolution, accurate-mass (HR/AM) Orbitrap detection was used for all MS analyses. An Accela ultra high-performance liquid chromatography (UHPLC or UPLC) system (ThermoScientific) was used for LC separation experiments. This system also features a photodiode array detector (DAD) for absorbance measurements across multiple wavelengths. Measurements were conducted under ambient conditions and employed a capillary inlet temperature of 250° C. A Model Fusion 200 syringe pump from Chemyx Inc. was used to pump analytes at set flow rates.
C. cVSSI Fabrication and Operation
cVSSI devices were fabricated by attaching a short piece (˜5.5 cm) of fused silica capillary (Polymicro) on the distal end of a VSSI device using a glass side as the thin, rigid substrate. The capillary was immobilized on the VSSI glass slide by glass glue. A detailed discussion of the fabrication of the VSSI device appears in Example 1. A schematic and photographs of the cVSSI device are shown in
The cVSSI device was activated using a function generator (Tektronix) and a power amplifier (Mini-Circuits) at frequencies of 93-97 kHz. For direct MS analysis, cVSSI was connected with 30-gauge PTFE tubing for sample introduction. The device was nominally placed in line with the inlet of the mass spectrometer at a distance of ˜5 mm. For LC-MS experiments, cVSSI was connected to the LC fluidic system using a MicroTight Union connector (Upchurch).
D. LC-MS and LC-MS/MS Analysis
A reverse phase C18 column was used for LC separation. 0.1% formic acid in water (A) and HPLC grade methanol (B) were used as the aqueous and organic mobile phases. Flow rate was set to 500 μL/min with the following gradient employed for metabolite separation: 0 min 5.0% B; 1.5 min 5.0% B, 8.5 min 30% B, 11.5 min 100% B, 14.5 min 100% B, 17.5 min 5.0% B. For each injection 20 μL of sample was used. The flow was split 10:1 for cVSSI into the mass spectrometer.
The same reverse phase column, solvent buffers, and flow rate were used for protein digest separations. Digestion of cytochrome c by pepsin was achieved by dissolving 10 mg of cytochrome c in 1.0 mL of deionized water with subsequent addition of 0.5 mg of pepsin. The solution was acidified to pH ˜3.5 by dropwise addition of acetic acid. A gradient program for the peptide separation is as follows: 0 min 5.0% B; 1 min 5.0% B, 18 min 50% B, 21 min 100% B, 24 min 100% B, 27 min 5.0% B, 30 min 5.0% B. For each injection 20 μL of sample was used. The flow was split 10:1 for cVSSI into the mass spectrometer.
Mass spectrometer settings were as follows. For full/precursor ion mass spectrum collection in LC-MS and LC-MS/MS analyses, a resolving power of 7×104 was used. For the LC-MS/MS analysis, the data-dependent approach used a resolving power of 1.75×104 for the fragment ion spectra and an m/z isolation window of 5. A value of 5 was used for the maximum number of MS/MS spectra to be acquired between precursor ion MS spectra collection.
E. Nebulization with Glass Capillary
The VSSI configuration of Example 1 was modified by attaching a short piece of fused silica capillary (5.5 cm long; 100 μm ID, 360 μm OD) on the distal end of a VSSI glass slide (
Relative positioning of the capillary and the glass slide was optimized as follows. With the VSSI configuration, the distal end of the glass slide allows for the highest vibration amplitude, so the capillary was first attached to the distal end of the glass slide using epoxy glue (
E. Droplet Size, Capillary Diameter, and Flow Rate
Relative droplet size distribution for cVSSI and VSSI was measured as described above. Both configurations showed a similar size distribution (
Capillary size and its impact on plume generation was studied as follows. 50, 75, 100, and 250 μm ID capillaries were tested. All sizes worked for cVSSI under the proper power input. Generally, as the inner diameter of the capillary decreased, a higher power input was required for nebulization. Based on previous studies, vibration at the VSSI sharp edge was critical to the nebulization phenomenon. As the ID of the capillaries decreased, the thickness of the capillary wall increased. A thicker wall, in turn, resulted in less efficient vibration at the tip so that higher power input was required. The 250 μm ID capillary had the thinnest wall but was more fragile than the other capillaries and was not as satisfactory as other ID capillaries when handling low flow rates (<10 μL/min). Despite the slight difference in power requirements, the 100 μm ID capillary was selected as optimal for additional experiments.
Flow rates for cVSSI were also optimized. Flow rates ranging from 1 μL/min to 1 mL/min were tested with a 100 μm ID capillary. cVSSI successfully nebulized liquid samples at all the flow rates in this range with the appropriate power input. At 1 μL/min, the power requirement for nebulizing fluid was ˜130 mW. As the flow rate increased to 20 μL/min, the power requirement increased to ˜260 mW. At 1 mL/min, a ˜760 mW power input was required to form a stable plume. These experiments demonstrated that cVSSI can work over a wide range of flow rates to accommodate different experimental setups. Even at the only tested high flow rates (˜1 mL/min), less than 1 W of power consumption was still reasonable. Here, the flow rate range was mainly limited by the capillary dimension rather than cVSSI. Using a 250 μm ID capillary, a flow rate of ˜2.8 mL/min flow rate was achieved using cVSSI. For flow rates <1 μL\min, a smaller ID capillary was required as the 100 μm capillary was prone to unstable flow with common syringe pumps.
F. Ionization Performance
Ionization performance of cVSSI in MS was analyzed as followed. A series of solutions containing a small molecule, a peptide, and proteins were tested using cVSSI-MS. Flow rate was set at 20 μL/min for all measurements. 10 μM solutions of acetaminophen, angiotensin II, cytochrome c, and ubiquitin in either acetonitrile:water (1:1) or in pure water resulted in successful analyte detection with cVSSI-MS (
Capillary-based direct injection in cVSSI enables more stable and convenient injection for quantitative analysis. A mass chronogram of a 0.5 min cVSSI injection is shown in
G. Coupling of cVSSI to HPLC
Coupling of cVSSI to HPLC for LC-MS analysis was also carried out. To accommodate the high-pressure HPLC pump and avoid leakage, a capillary connector was used to couple a cVSSI source to the HPLC fluidic system (
H. Metabolomics Experiments
A series of representative metabolites including endogenous metabolites (L-valine, dopamine, guanosine, guanine) and exogenous metabolites (sucrose, acetaminophen, caffeine, aspartame, benzoic acid) were mixed in water with each compound at ˜100 ppm concentration. The sample was introduced onto a reverse phase C18 HPLC column at a flow rate of 500 μL/min. Water with 0.1% formic acid and methanol were used as the aqueous and organic phases, respectively. The eluent was introduced directly on the cVSSI device through a capillary connector and detected using an Orbitrap mass spectrometer. As shown in
I. Proteomics Experiments
LC-MS/MS experiments were conducted for a pepsin digest of cytochrome c to test the suitability of cVSSI-MS/MS for peptide identification. After LC-cVSSI-MS/MS analysis, peptides were identified by a protein database search. Overall, ˜75% sequence coverage was obtained for cytochrome c protein using the protein database approach. The incomplete sequence coverage could result from low-quality MS/MS spectra for some peptides or from the fact that the precursor ions for some peptides containing the missing sequences simply are not selected for MS/MS analysis. To determine whether or not peptide assignments were missed by the protein database search, the ion chromatogram was searched manually. Here, the ion signal was averaged over retention time (tR) windows of 2 min in duration. Peptide ion assignments, made by accurate mass assessments, are provided in Table 1.
aPeptic peptide sequence obtained from the Peptide Mass software at https./web.expasy.org/peptide_mass/. Peptides containing the two cysteine residues were observed with the attached heme group.
bExperimental m/z (monoisotopic) obtained by hand from the ion chromatogram
bTheoretical m/z (monoisotopic) obtained from the Peptide Mass software at https://web.expasy.org/peptide_mass/
dMass accuracy expressed as ppm
eRetention time window that was averaged to obtain the mass spectrum for peak picking. Times are given in minutes.
From the stepwise precursor ion analysis, a total of 78 peptides were identified. These included species ranging in size from 2 to 29 amino acid residues and in charge states of +1 to +6. Several heme-containing peptides were also observed. Considering the sequences of those peptides, 100% sequence coverage of the protein was demonstrated by the peptides shown in Table 1. In general, cVSSI was shown to be sufficiently efficient for the ionization of peptides in proteomics studies. It is noted that a split-flow geometry was employed. cVSSI can be conducted at much higher flow rates because there is no impetus for the large number of droplets to enter the MS inlet beyond gas-flow entrainment, so a 10-fold split was employed, which helped maintain cleanliness of the source.
A. Design and Fabrication of VSSI Probe Capillary Electrophoresis
A conceptual diagram of the capillary and probe is depicted in
The VSSI probe was fabricated from a borosilicate capillary that was pulled to approximately 50 μm outer diameter at the tip (
B. VSSI Probe Capillary Electrophoresis Proof of Principle (50 μm ID Capillary)
Prototype VSSI probe sources were fabricated and used to demonstrate the functionality of the approach. In one example, spray was generated using an acoustic probe fabricated from a pulled glass capillary at pH 5 and 6.5. The probe was fabricated with a 50 μm ID capillary and 25 μm platinum electrode to ground the separation current. Separations were performed with background electrolyte adjusted to two different pH values. The separations were reproducible in time and intensity; see Table 2 below.
For proof of concept experiments, the beta-blocker drugs pindolol, metoprolol, and acebutolol were used as analytes. Each has a conjugated pi-electron ring system for verification using UV-absorbance in a traditional CE device. When benchmarked against a traditional capillary electrophoresis separation composed of a 50 cm long 50 μm ID capillary with an effective length to the detection window of 40 cm with UV-absorbance detection, the migration time of the pH 6.5 data obtained with the vibrational spray (
The effect of flow rate on spray ionization and role of electric field on vibrational spray were performed. These results are summarized in Tables 3 and 4 and demonstrate that there is a flow rate dependence with respect to ionization efficiency. These results do not confirm that the electrophoresis is necessary to drive the spray, but do indicate that flow must be delivered at the end of the capillary to complete the electrical spray and to deliver the molecules to the mass spectrometer through a droplet train that is desolvated en route to the mass analyzer.
C. VSSI Probe Capillary Electrophoresis Proof of Principle (100 μm ID Capillary)
Prototype acoustic spray sources were fabricated and used to demonstrate the functionality of the approach. In one example, spray was generated using an acoustic probe fabricated from a pulled glass capillary at near neutral pH. Angiotensin and sialylglycopeptide were each separated in a 60 cm long, 100 μm ID fused silica capillary under reversed polarity with an applied voltage of 5 kV. A 25 μm diameter platinum wire was affixed across the capillary orifice and connected to ground to complete the electrophoresis electrical circuit using techniques described above and/or previously reported for fabrication of integrated capillary electrophoresis-electrochemical systems. The separation current of 16 μA remained stable throughout multiple runs. A prototype acoustic source was composed of a 100 μM ID capillary modified with a semi-permanent cationic surface coating. The device was used to separate and detect 0.3 mg/mL angiotensin in 25 mM pH 6.5 ammonium acetate or 0.15 mg/mL sialylglycopeptide in 25 mM pH 4.0 ammonium acetate analyzed with a Q Extractive (
Chemicals and Reagents. Ammonium acetate (73594), acetic acid (A6283), pindolol (P-0778), acebutolol (A-3669), soybean trypsin inhibitor (T9128), and ubiquitin (U6253) were purchased from Millipore Sigma (Burlington, Mass.). Ammonium hydroxide (44273) was purchased from Fisher Scientific (Waltham, Mass.). Somatostatin and oxytocin were purchased from American Peptide (Sunnyvale, Calif.). Deionized water was filtered with an Elga Purelab ultra water system (Lowell, Mass.). Solutions were filtered using 0.45 μm PTFE filters (VWR).
CE-VSSI Probe Fabrication. Fused silica capillary (50 μm i.d., 365 μm o.d., Polymicro Technologies, Phoenix, Ariz.) was cut to a length of 40 cm, and 0.5 cm of the polyimide coating was burned off the outside on both ends. The ends were checked under a microscope for clean, straight cuts. A 25 μm platinum wire (PT005113, Goodfellow, Huntingdon, England) was cut to approximately 1 cm in length and bent at two 90° angles in a “U” shape. This wire was maintained across the front orifice of the capillary using a small amount of 1 min epoxy 1366072, Henkel, Düsseldorf, Germany). A thicker wire cut to about 5 cm was attached to the thinner wire via conductive epoxy (8331-14G, MG Chemicals, Ontario, Canada) to create an electrical connection. After the conductive epoxy cured, it was covered with an additional layer of 1 min epoxy (1366072, Henkel) for mechanical stability and to insulate the connection. The end of the larger wire was soldered with a drop of lead solder. Capillaries were allowed to cure completely before they were aligned with the VSSI spray probe.
To fabricate the VSSI spray probes, a P-2000 capillary puller (Sutter Instrument Company, Novato, Calif.) was used to pull 75 mm long capillaries with an I.D. of 0.4 mm (no. 1-000-800/12 Drummond Scientific Company, Broomall, Pa.). Parameters used were HEAT=700, FIL=4, VEL=55, DEL=200, and PUL=175. A pulled glass capillary was attached to one end of a glass microscope slide and a piezoelectric transducer (7BB-27-4 LO, Murata). The piezoelectric transducer was glued to the other end as reported previously (Ranganathan, N., et al., J. Am. Soc. Mass Spectrom. 2019, 30, 824). The probe was attached to a function generator (AFG-1062, Tektronix, Beaverton, Oreg.) and amplifier (7500, Krohn-Hite, Brockton, Mass.) and driven with a square wave, having a frequency in the range of 92-96 kHz and an amplitude in the range of 30-140 mVpp, depending upon the size and geometry of the glass probe. Each spray probe has a slightly different geometry which means that one frequency and amplitude is not applicable to all probes. In general, larger probes (i.e., >50 μm o.d. tip) require a larger amplitude than small probes (i.e., ≤50 μm o.d. tip).
The capillary and spray probe were aligned on the microscope with the tip of the spray probe touching the wall of the capillary near the orifice. The glass probe was fixed on the corner of the glass coverslip with no more than 4 cm extending over the edge, as depicted in prior work.(43) This allowed the probe to vibrate freely when the frequency and amplitude are applied. A 90° angle relative to the capillary was chosen so that sufficient contact with the capillary could be made. Since the probe must touch the orifice of the capillary, this angle allowed for the most contact between the probe and the capillary tip. The spray probe was placed parallel to the platinum electrode or at a small angle relative to the platinum electrode to ensure that the probe and electrode did not come into contact. This was done because placing the probe perpendicular to the electrode often resulted in severing the platinum electrode. The integrated probe and capillary assembly were placed within 2 mm of the transfer line.
CE-VSSI-MS Separation and Analysis. A lab-built instrument composed of a nitrogen gas tank to supply pressure and a high voltage power supply (CZE1000R, Spellman, Hauppauge, N.Y.) was constructed as previously described (White, C. M.; Hanson, K. M.; Holland, L. A. Analytical Sciences Digital Library: http://www.asdlib.org/2005, ASDL Entry 10031). Separations were carried out using bare fused silica capillaries with a total and effective length of 40 cm, an inner diameter of 50 μm, and an outer diameter of 365 μm. At the beginning of each day, flushes were done at 41 kPa (6 psi) with 0.1 N ammonium hydroxide for 60 min, water for 10 min, and buffer for 30 min with the acoustic spray off. In between runs, the capillary was flushed for 1 min with background electrolyte with the VSSI active during the flush. If the probe was not active during the 1 min flush applied in between the CE runs, then liquid accumulated at the capillary tip and entered the probe. When acoustic spray was restored, the additional liquid in the probe was ejected and an increase in the MS signal was observed for a few seconds. The injection was either 10 kV for 2 or 4 s and the separation voltage was 10 kV applied in normal polarity. Scanning ranges on the MS were mass-to-charge (m/z) 165-400 for β-blockers, 400-1700 for peptides, and 500-4000 for protein. The MS capillary temperature was set to 350° C. An LTQ XL or Q-exactive mass spectrometer equipped with LTQ Tune Plus software (version 2.7) was used to collect the data (Thermo Fisher Scientific, San Jose, Calif.). Data were processed using Thermo Fisher Scientific Xcalibur (version 4.1) and Microsoft Excel (2016, Microsoft, Redmond, Wash.).
The limit of detection (LOD) and limit of quantification (LOQ) were determined using LOD=ks(C/(H−h)), where k is the confidence factor (i.e., 3 for LOD and 10 for LOQ), s is the standard deviation of the noise, C is the sample concentration, H is the average signal of the analyte, and h is the average signal of the noise. The standard deviation of the noise was determined using the same number of points that comprised the analyte peak, but from a portion of the baseline just before the analyte peak eluted.
CE-UV Separation and Analysis. Bare-fused silica separations were conducted using a ProteomeLab PA800 capillary electrophoresis system (Sciex, Redwood City, Calif.). Capillaries had a total length of 50 cm, an effective length of 40 cm, and an inner diameter of 50 μm. The capillary preparation and separation were the same as those used for the VSSI-MS analyses. To maintain the same electric field strength used on the CE-VSSI-MS system, the separation voltage was +12.5 kV. The analyses were performed using UV absorbance detection at a wavelength of 200 nm. The cartridge temperature was set to 19° C. for flushes and 25° C. for separations. Data were collected and analyzed using 32Karat software (version 7.0, Sciex).
Interface Design and Implementation. The elements of the CE-VSSI interface are the probe, grounding electrode, blunt capillary tip, and acoustic generator. The arrangement of each component is shown in
Prior to installing the CE-VSSI device on the mass spectrometer, each device was assembled and tested to ensure that a plume of droplets was observed. This was done by applying a pressure equivalent to the rate of the electroosmotic flow and adjusting the applied frequency and amplitude until a strong and stable plume was observed that lasted for 3 min. The stability of the droplet plume was also tested in the presence of electrophoresis. The VSSI spray system was compatible with both 75 and 50 μm i.d. capillaries; however, the larger bore capillary was susceptible to siphoning. Measures that were taken to reduce siphoning included leveling the setup each time and maintaining the liquid above the bottom of the capillary no higher than 0.5 cm. 45 The 50 μm inner diameter of the separation capillary generated sufficient electroosmotic flow to sustain both electrophoresis and a visible plume of droplets.
Evidence of Acoustic Driven Spray. Application of the device demonstrated the significance of the VSSI probe for droplet formation leading to sample transfer to the mass spectrometer rather than direct spray at low CE flow rates. CE was initiated using a background electrolyte of 25 mM acetic acid buffered to pH of 5 that also contained 10 μM pindolol. Under these conditions the pindolol is cationic and easily ionized. The approximate electroosmotic flow rate at this pH was 70 nL/min at a field strength of 250 V/cm. The acoustic source was manually cycled on and off with no interruption of the CE voltage. Turning the acoustics off coincided with a drop in the ionization intensity (
The nebulized droplets are generally, but not always, ejected at a right angle to the vibrating probe for different probes and capillaries coupled to create CE-VSSI. This is attributed to subtle differences in the probe geometry and alignment. Although the mechanism of droplet formation is different, a similar observation was reported with CE-ESI, 11 which was rectified through the use of a nitrogen chamber. A less sophisticated nitrogen chamber was constructed and used with VSSI with a goal of directing more droplets into the MS and making a more uniform environment for ionization since the VSSI interface was developed with an open platform for the ion source. The peak areas obtained for the separation and detection of a sample of 1 μM pindolol in the presence and absence of the nitrogen chamber, which were 300,000±100,000, and 180,000±80,000, respectively, were not significantly different. Improvements in the design as well as optimization of the nitrogen flow may dramatically enhance the performance. Additional studies are needed to define the factors that orient the direction of the plume in order to maintain efficient ion transfer.
To test the effects of flow rate on signal, pindolol was separated at different applied voltages, and the migration velocity was used as a measure of flow rate. The relationship between migration velocity and peak area was linear (R2=0.94). This study was performed using two different CE-VSSI devices with each capillary spanning three points (i.e., 0.15, 0.23, and 0.41 cm/s or 0.23, 0.54, and 0.74 cm/s). At higher pindolol velocity, a higher peak area was obtained as more analyte was delivered to the MS. Flow rates below the minimum velocity of 0.15 cm/s could not be evaluated because the spray was unstable at these low flow rates. Conversely, rates above the maximum velocity were not tested because the separation currents approached levels that lead to Joule heating (i=39 μA).
The ionic strength of the background electrolyte affects the rate of electroosmotic flow as well as ionization. The impact of four different concentrations (ranging from 10 to 75 mM) of ammonium acetate were tested. As ionic strength was increased successively, the peak area of pindolol decreased. At ammonium acetate concentrations of 10, 18, 25, and 75 mM, peak areas were 9,400,000±800,000, 3,300,000±300,000, 1,400,000±100,000, and 1,100,000±100,000, respectively. The same trend was observed for acebutolol, which at ammonium acetate concentrations of 10, 18, 25, and 75 mM, had peak areas of 5,200,000±400,000, 1,600,000±200,000, 510,000±10,000, and 490,000±60,000, respectively. While these data suggest that lower ionic strengths should be used to achieve better signal, other aspects of the background electrolyte concentration must also be considered. For example, the concentration of the background electrolyte may affect the separation through nonspecific adsorption to the capillary surface.
The compatibility of VSSI with different volatile background electrolytes was evaluated. Pindolol was separated and detected with three different electrolytes systems at near-neutral or basic pH values each at a concentration of 25 mM. Ammonium acetate and ammonium bicarbonate both had a measured pH value of 6.5. Bicarbonate is an effective buffer at this pH value; whereas acetate does not serve as a buffer at pH 6.5. Peak areas resulting from the near-neutral background electrolytes, which were 280,000±10,000 for ammonium acetate and 360,000±60,000 for ammonium bicarbonate, were similar. However, ammonium hydroxide buffered at pH 10 yielded a 10-fold higher signal with an area of 2,900,000±200,000. This increase of positive ions at highly basic pH values has previously been reported in the literature as the “wrong-way round” principle (Mansoori, B. A., et a., Rapid Commun. Mass Spectrom. 1997, 11, 1120-1130).
Separation and Detection with CE-VSSI-MS Compared to CE-UV. The CE-VSSI-MS system was used to separate two β-blockers at a near neutral pH in order to compare the separation with CE-UV. A background electrolyte of 25 mM ammonium acetate at pH 6.5 was used, which generated an electroosmotic flow of approximately 110 nL/min. A β-blocker mixture composed of 1 μM (0.25 μg/mL) pindolol and 1 μM (0.34 μg/mL) acebutolol was used to characterize the separation and device performance (
The separation efficiency of 80,000 plates/m was comparable to that obtained with the UV detection (Tables 5 and 6). The theoretical plates are 80%-95% of those observed with the capillary electrophoresis UV system, and migration times vary by no more than 7% with either β-blocker. While most CE-ESI-MS separations are performed at acidic conditions to eliminate surface adsorption and facilitate ionization, these data indicate that CE-VSSI is compatible with capillary electrophoresis operated under near neutral conditions that generate electroosmotic flow. The plate counts obtained with VSSI using a background electrolyte at pH 6.5 approach plate counts reported in the literature of 170,000 plates/m for cationic metabolites (Portero, E. P. and Nemes, P., Analyst 2019, 144, 892- 900), which was achieved under conditions of low pH. With acidic background electrolyte in bare fused silica capillary, the analyte migration is based solely on electrophoretic mobility resulting in longer run times. If flow is superimposed to stabilize the electrospray and speed the separation, the efficiency of the electrophoresis will be reduced. In other instances, it has also been noted that the process of electrospray itself may superimpose laminar flow in capillary electrophoresis (do Lago, C. L., et al. Electrophoresis 2014, 35, 2412-2416; and Busnel, J.-M., et al., Anal. Chem. 2010, 82, 9476- 9483).
aDistance to detector is 40 cm.
bValues for peak width were obtained with 2 significant figures.
cValues for peak width were obtained with 4 significant figures.
dCalculated by determining the width at base (w) as N = 16t2/w2
The CE-VSSI interface was also applied to the separation of a sample containing 50 μM (82 μg/mL) somatostatin and 50 μM (50 μg/mL) oxytocin. Peptides were injected electrokinetically (10 kV, 2 s), corresponding to a mass of 370 pg somatostatin and 210 pg oxytocin loaded into the capillary. It should be noted no effort was made to desalt the peptides prior to analysis and subsequently sodium adducts were observed for oxytocin. Peptide separations had similar performance relative to CE-UV data (
The utility of CE-VSSI-MS for protein analysis was evaluated by injecting and separating ubiquitin mixed with a commercial soybean preparation that primarily contained trypsin inhibitor. The benefit of the VSSI interface is depicted in
While the concentrations of the proteins and peptides in the soybean trypsin inhibitor standard is not known, the 10 kV 4 s injection of proteins corresponds to 580 μg ubiquitin. The peak areas for ubiquitin and trypsin inhibitor were 33,000,000±9,000,000 and 400,000±400,000, respectively. The worse precision of trypsin inhibitor relative to ubiquitin is attributed to the presence of the peptides and protein variants in the stock. This adversely impacts the ionization efficiency of this anionic protein, leading to a substantially lower signal. The plate counts for ubiquitin and trypsin inhibitor are lower or the same with CE-VSSI-MS as compared to CE-UV (Table 5). The trace in
The ubiquitin and trypsin inhibitor proteins were selected because with neutral or basic separation buffers, most other proteins adsorb to the bare fused silica surface and produce broad peaks. Further optimization of the electrophoretic separation is underway to reduce surface adsorption of the protein to achieve higher efficiency separations. Finally, although the trypsin inhibitor was desalted through buffer exchange with a 10 kDa molecular weight cutoff filter (Merck Millipore UFC501024, Burlington, Mass.), sodium adducts were observed in the extracted ion electropherogram. Applying insource ion activation will improve the technique further by declustering the protein adducts.
Discussion. This example demonstrates the utility of the CE-VSSI-MS interface disclosed herein. Under the conditions used to evaluate VSSI performance in the present disclosure, the performance was similar to sheathless and coaxial-sheath CE-ESI-MS. The CE-VSSI maintained the CE separation efficiency and was compatible with different volatile background electrolytes, ionic strength, and enabled separations at near-neutral pH. Organic modifiers were not required to assist with droplet formation. The present example demonstrates the utility of this first working example of the disclosed interface for CE-MS analysis with small molecules, peptides, and proteins. Beyond performance, the disclosed CE-VSSI is inexpensive given that probes are fabricated from pulled glass tubes costing $0.10 each and piezoelectric transducers available for under $1. Collectively, these attributes of CE-VSSI may offer advantages to a variety of applications including ionization under native conditions (i.e., neutral pH values and in the absence of organic solvents) or field measurements where lower cost interfaces are needed. Finally, the disclosed devices and processes are readily adaptable to conventional commercial instruments to increase the accessibility of the disclosed techniques.
Materials and Reagents. High performance liquid chromatography (HPLC) grade water, nuclease-free water, potassium chloride, and ammonium acetate (NH4OAc) were purchased from Fischer Scientific (NJ, U.S.A.). Trimethylammonium acetate (TMAA) was obtained by slowly adding 4.3 M acetic acid to 50 mL of 4.3 M trimethylamine (TCI chemical) solution until the pH was around 7.0, and this process was monitored by a pH meter (Mettler Toledo, Ohio). Acetic acid, fondaparinux sodium (C31H43N3Na10O49S8, m.w. 1728.1 g/mol) and chondroitin disaccharide Δdi-6S sodium salt (C14H19NO14SNa2, m.w. 503.34 g/mol) were purchased from Sigma-Aldrich (MO, U.S.A.). Insulin (human) and angiotensin 2 (human) were purchased from Alfa Aesar (MA, U.S.A.). Ubiquitin (˜8.5 kDa) was purchased from Boston Biochem (MA, U.S.A.). Myoglobin (˜17 kDa) was purchased from Sigma-Aldrich (St. Louis, Mo., U.S.A.). All DNA oligonucleotides used in this work, d(CATATATG), d(ACGCGCGT), 56-mer ssDNA, and human telomeric G-quadruplex sequence d(TT(GGGTTA)3GGGA) were pur-chased from Integrated DNA Technologies, Inc. (Coralville, Iowa, U.S.A.). All the chemical reagents and oligonucleotides were used without further purification.
Fabrication of Pulled-Tip Capillary and cVSSI Device. Pulled-tip capillaries were prepared using a Laser-Based Micropipette Puller Sutter P-2000 (CA, U.S.A.). Program settings for the pulled fused silica capillary were HEAT 750, FIL 4, VEL 60, DEL 200, and PUL 175. Before being bonded to the No. 1 cover glass slide (24×60 mm, VWR), the pulled capillary was soaked in 30% hydrofluoric acid for ˜2 min until the end I.D. of the pulled capillary is the desired I.D. (9-20 μm), and this process was monitored under the microscope. The fabrication procedures of each cVSSI device is similar to our previous report (Ranganathan, N., et al., J. Am. Soc. Mass Spectrom. 2019, 30, 824-831; Li, X., et al. Rapid Commun. Mass Spectrom. 2018, na DOI: 10.1002/rcm.8232). Briefly, a piezoelectric transducer is first attached to a glass cover slide by epoxy glue, and the pulled capillary is bonded to the same glass slide by glass glue. The cVSSI device was activated using a function generator (RIGOL DG4102) and a power amplifier (Krohn-Hite 7500). The working frequency of each cVSSI device was determined by scanning frequencies from 90 to 105 kHz under a constant voltage input of 10 Vpp. The operational voltage is then determined to be the minimum voltage input that produces a stable plume under the selected working frequency. The normal working frequencies and amplitudes are 93-97 kHz and 5-10 Vpp, respectively. A piece of 20 cm long PTFE tubing (#30 thin wall tubing, Cole-Parmer Instrument Company) was used to connect the sample syringe and the pulled capillary. A 5 cm long Pt wire (Diameter: 20 μm) was inserted into the PTFE tubing as an electrode, and the end of the Pt electrode was ˜1 cm away from the end of the PTFE tube (
Preparation of the DNA Duplex and G-Quadruplex. For all DNA samples, the stock solution concentrations were determined before an annealing process was employed using the Thermo Scientific Nanodrop 2000 Spectrophotometer. Stock solution of 100 μM ssDNA, d(CATATATG) was prepared in purified water and diluted to 10 μM in 100 mM NH4OAc. The DNA duplex of self-complementary strand d-(ACGCGCGT) was prepared by diluting the stock solution to reach 20 μM ssDNA and annealing was performed in 100 mM NH4OAc at 94° C. in an oil bath for 2 min. This was cooled to room temperature overnight to obtain 10 μM DNA duplex solution. Stock solutions of 1 M TMAA and 1 mM KCl were used for G-quadruplex DNA solutions. The G-quadruplex DNA stock solution was diluted to reach 10 μM ssDNA and quadruplex structure was prepared by mixing 100 μM ssDNA, 100 mM TMAA, and 100 or 500 μM KCl in water, annealing at 85° C. for 5 min then followed by cooling to room temperature overnight. Final concentration of G-quadruplex DNA is 10 μM as each single strand folds to create the quadruplex structure.
Mass Spectrometry Analysis. A Q-Exactive Hybrid Quadruple Orbitrap mass spectrometer and a LTQ-XL mass spectrometer (Thermo Fisher, San Jose, Calif., U.S.A.) were used for mass spectrometry measurements. Both mass spectrom-eters are equipped with Ion Max Ionization Sources with HESI probe for ESI ionization. For Q-Exactive mass spectrometric analysis, the resolving power was set at 70000, and the inlet capillary temperature was maintained at 100° C. For experiments using the HESI source, voltage, and sheath gas flow rates were optimized for each analyte to achieve the highest ion intensities. Typical ranges for bias voltage and sheath gas rates were −3 to −4 kV and 15 to 30 absolute units (a.u.), respectively. For experiments using a cVSSI source plus voltage, the same instrument setting as HESI experime is was used, except that the applied voltage was ˜−1.1 to −1.4 kV and no sheath gas was applied. For ESI analysis with the LTQ-XL mass spectrometer, the capillary voltage, tube lens voltage, and the mass inlet capillary temperature were set at −10.00 V, −100.00 V, and 275° C., respectively. Without special notice, the sample flow rates for both the Q-Exactive and LTQ-XL HESI were 10 μL/min, and sample flow rates for VSSI analysis were 1 μL/min. The S/N of features in as spectra was calculated based on the following equation:
where Ipeak is the peak intensity of the analyte (above the average of the noise) and σSTD of the noise is the standard deviation of the noise. For each spectrum, the noise region was selected a few m/z before or after the analyte peak, and the noise region does not include any detectable ion peak.
Enhancing Ion Signal Levels in Negative Ion Mode with cVSSI. Because the cVSSI process allows the generation of a plume independent of the electrical properties of the solvent, it is speculated that this process should provide benefits to ESI experiments when the required voltage for ESI onset is high. We therefore first examined if applying cVSSI to a pulled-tip capillary with a negative bias voltage can enhance signal levels of DNA molecules in negative ion mode analyses. DNA mass spectrometry is primarily performed in negative ion mode because DNA contains a negatively charged phospho-diester backbone that facilitates negative ion formation by ESI (Potier, N., et al., Nucleic Acids Res. 1994, 22, 3895-3903; Tretyakova, N., et al., Chem. Rev. 2013, 113, 2395-2436; and Hua, Y., et al., J. Am. Soc. Mass Spectrom. 2001, 12, 80-87). This highly polar nature of DNA presents significant challenges with regard to native MS analysis, requiring significant bath gas usage to aid the desolvation process. Nano-ESI circumvents this requirement (Banerjee, S. and Mazumdar, S., Int. J. Anal. Chem. 2012, 2012, 1; and Banoub, J. H., et al., Chem. Rev. 2005, 105, 1869-1915); however, it provides unique challenges for stable and efficient ion production (Rahman, M. M., et al., Analyst 2013, 138, 6316-6322). For example, the larger influence of corona discharge has a significant effect on the overall stability of the process and thus affects the reproducibility of the measurement (McClory, P. J. and Hakansson, K. Anal. Chem. 2017, 89, 10188-10193). This is unfortunate especially in cases where only limited sample is available. To examine the potential role of cVSSI in DNA analysis, experiments were designed to compare ion production of a DNA duplex d(ACGCGCGT)2 sample for conditions in which voltage biasing (˜1.27 kV) of the emitter tip (ID: ˜15 μm) was employed alone with that of the addition of cVSSI. The total ion chronogram is presented in
Corona Discharge Suppression by cVSSI. Part of the enhanced signal levels in negative ion ESI could be attributed to discharge suppression by cVSSI. To test this hypothesis, a digital microscope was employed to monitor the emitter tip (ID: ˜18 μm) during ESI experiments. As shown in
cVSSI Stabilizes the NanoESI in Negative Ion Mode. The above results demonstrate the role of cVSSI in suppressing corona discharge and enhancing ion signals in negative ion mode analyses of DNA in aqueous solutions. In many cases, cVSSI salvages the signal from corona discharge as no detectable DNA peaks are obtained by ESI alone. The emitter has a very narrow working voltage range from −0.85 to −1.01 kV. The performance degrades rapidly as the applied voltage deviates from the optimal value (−0.9 kV). Applying cVSSI allows a much wider range of working voltages from −0.3 to −2.5 kV with the best peak performance observed at −1.3 kV. There are two major advantages associated with the extended voltage range. First, a higher optimal voltage is achieved with cVSSI compared to direct electrospray alone, which results in ˜6-fold improvement in ion intensity (
Ion Production Enhancement from VSSI Compared with Commercial ESI Sources. The experiments described above demonstrate the benefits of applying cVSSI to the ESI emitter tip over using ESI alone in negative ion mode when spraying DNA from aqueous solutions. The performance of using cVSSI plus voltage was compared with commercial ESI sources equipped with nebulization gas. Nebulization gas is the most widely used and amenable instrumentation method to alleviate the discharge issue in negative ion mode. Due to the challenging working conditions of nano-ESI for negative ion production of molecules in aqueous solutions, as shown above, many native MS experiments are performed using commercial ESI sources equipped with nebulization gas capabilities (Khristenko, N., et al., J. Am. Soc. Mass Spectrom. 2019, 30, 1069-1081; Porrini, M., et al., ACS Cent. Sci. 2017, 3, 454-461; and Gabelica, V., et al., J. Am. Soc. Mass Spectrom. 2018, 29, 2189-2198).3 It is instructive to compare the ionization efficiency of cVSSI plus voltage with that obtained from a well-engineered commercial ESI source. For the following comparisons, HESI sources on the Q-Exactive mass spectrometer and the LTQ-XL mass spectrometer were optimized and compared with the device that couples cVSSI with electrospray voltage. In brief, ion signal levels are again dramatically enhanced with the combined approach.
A series of solutions were tested, including nucleic acids, oligosaccharides, peptides, and proteins, in negative ion mode.
In addition to the DNA samples, a similar level of improvement was observed for oligosaccharides, peptides, and proteins, when comparing the HESI and the cVSSI plus bias voltage ion sources on the LTQ-XL mass spectrometer. For oligosaccharides, 10 μM of chondroitin disaccharide Δdi-6S sodium (
Angiotensin 2 (
This example demonstrates that the cVSSI plus voltage source provides better ion intensity and S/N than the commercial HESI source does. Replacing the nebulization gas with cVSSI to suppress the discharge enables an ionization source setup that has a significant improvement in total ion intensity detected. Part of the enhancement could come from the use of a pulled fused silica capillary tip instead of the stainless-steel capillary used in the HESI system. Replacing the nebulization gas with cVSSI to suppress the discharge could also contribute to the enhancement. This contrast between the nebulization and cVSSI process is rendered more striking by the fact that the flow rates (and thus sample consumption) in HESI experiments are 5-10-fold higher.
The improvements in ion signal level and S/N have clear implications with regard to different analyses. For example, S/N improvements would impact the ability to distinguish precursor ions in complex mixtures such as those encountered in “omics analyses”. That is, S/N improvements allow the detection of lower-signal species in the presence of higher-signal ions (Counterman, A. E., et al., J. Am. Soc. Mass Spectrom. 2001, 12, 1020-1035; Faktor, J., et al., Proteomics 2017, 17, 1600323; Bantscheff, M., et al., Anal. Bioanal. Chem. 2007, 389, 1017-1031; and Yates, J. R., et al., Annu. Rev. Biomed. Eng. 2009, 11, 49-79). In the case of ion signal level enhancements, a clear advantage is provided to tandem MS and multistage tandem MS ((MSn); see McLuckey, S. A., et al., J. Am. Soc. Mass Spectrom. 1992, 3, 60-70; McLuckey, S. A. and Habibi-Goudarzi, S., J. Am. Soc. Mass Spectrom. 1994, 5, 740-747; Hengel, S. M. and Goodlett, D. R., Int. J. Mass Spectrom. 2012, 312, 114-121; Heller, M., et al., Mol. Cell. Proteomics 2007, 6, 1059-1072; and Kang, H., et al., J. Am. Soc. Mass Spectrom. 2007, 18, 1332-1343). Here, the ability to dependent on ion numbers in the precursor ion selection step. This is especially true for species that may not undergo facile fragmentation or when attempting to observe a low-frequency ion fragment. Finally, enhancements in S/N levels of ions from aqueous media enable the coupling of separation techniques that rely on such media. Thus, the enhancements in ion signal level and S/N realized here with cVSSI provide immediate advantages fora number of fields employing MS analysis.
Potential Applications in Native MS Analysis. An increasing area of interest in biological mass spectrometry is the characterization of biomolecular structure (Cheatham, T. E., et al., Curr. Protoc Nucleic Acid Chem. 2001, 5, na; Baker, E. S., et al., J. Am. Soc. Mass Spectrom. 2005, 16, 989-997; Zucker, S. M., et al., J. Am. Soc. Mass Spectrom. 2011, 22, 1477-148; Kondalaji, S. G., et al., J. Am. Soc. Mass Spectrom. 2018, 29, 1665-1677; Zhang, W., et al., Nat. Commun. 2019, 10, 79; and Zhang, W., et al., Anal. Chem. 2019, 91, 6986-6990). To evaluate the potential of cVSSI plus voltage for structure characterization, experiments have been conducted for molecules for which it has been proposed that native MS allows the preservation of solution structure in the gas phase (Wyttenbach, T. and Bowers, M. T. J. Phys. Chem. B 2011, 115, 12266-12275). The first study involves the examination of the globular protein ubiquitin which was examined in both positive and negative ion mode. The second study involves the examination of the formation of a G-quadruplex DNA structure in solution. Each is described in greater detail below.
Positive and negative ion mode experiments have been conducted for a solution of the globular protein ubiquitin. Ubiquitin is a well-studied protein for native MS analysis, and the relationship between charge state distribution and solution structures has been reported before (El-Baba, T. J., et al., J. Am. Chem. Soc. 2017, 139, 6306-6309). Therefore, it is a good indicator for whether or not the cVSSI process disrupts the native structure of biomolecules. For these experiments, we also tested positive ion mode conditions in addition to those for negative ion mode analysis as most of the existing studies for ubiquitin are performed in positive ion mode. Ion production using a commercial ESI source was compared to that using a cVSSI source plus voltage. In positive ion mode, ESI produces two charge states comprised of [M+6H]6+ (m/z 1428.58) and [M+5H]5+ (m/z 1713.92) ions (
Nucleic acids are another important class of biomolecules that can assume 3D structures in solution. While nucleic acids can be studied in both positive and negative ion mode, studies suggest that ions produced in negative ion mode better reflect their solution structure (Rosu, F., et al., Int. J. Mass Spectrom. 2006, 253, 156-171). Therefore, native DNA/RNA mass spectrometry experiments are usually performed in negative ion mode. Some biomolecular structures require solutions of significant ionic strength in order to form. An example is the G-quadruplex DNA, which can form in solutions containing potassium due to charge-dipole stabilization of the G-quartets. To demonstrate that the new VSSI source can preserve the G-quadruplex structure similar to ESI (Marchand, A. and Gabelica, V. J. Am. Soc. Mass Spectrom. 2014, 25, 1146-1154), experiments were conducted with the human telomeric G-quadruplex DNA (TTGGGTTAGGGTTAGGGTTAGGGA) sequence (G4). As above, experiments were conducted using the cVSSI plus voltage device. Samples containing two different concen-trations (100 and 500 μM) of KCl were examined by MS.
Further Discusssion. Combining the disclosed cVSSI processes with a voltage can effectively suppress the discharge in conventional ESI experiments, thereby improving the signal quality significantly. Overall, the disclosed cVSSI processes are easy and cost-effective to implement with a wide range of working flow rates. When coupled to a pulled-tip capillary, it can handle flow rates of 0.2-1 μL/min for small volume samples. The disclosed cVSSI processes can also work with normal capillaries (ID approximately 100 μm) to accommodate high flow rates. All the components of the cVSSI system can be purchased directly with a cost of less than $10 per device.
The present example has emphasized negative ion mode analyses is because such studies are significantly hindered in native MS, as evidenced by the fact that, for the most part, they require auxiliary methods/techniques to obtain useful analyses. Additionally, the signal enhancement provided by cVSSI is significantly greater for negative ion mode studies. That said,
It should be emphasized that the above-described embodiments of the present disclosure are merely possible examples of implementations set forth for a clear understanding of the principles of the disclosure. Many variations and modifications may be made to the above-described embodiment(s) without departing substantially from the spirit and principles of the disclosure. All such modifications and variations are intended to be included herein within the scope of this disclosure and protected by the following claims.
This application claims the benefit of U.S. Provisional Application No. 62/872,702, filed on Jul. 11, 2019, which is incorporated herein by reference in its entirety.
This invention was made with government support GM128577-01 and GM114494 awarded by the National Institutes of Health and CHE1553201 awarded by the National Science Foundation. The government has certain rights in the invention.
| Number | Name | Date | Kind |
|---|---|---|---|
| 8011230 | Watanabe | Sep 2011 | B2 |
| 8450682 | Hiraoka | May 2013 | B2 |
| 9058966 | Otsuka | Jun 2015 | B2 |
| 9230787 | Kyogaku | Jan 2016 | B2 |
| 9269557 | Otsuka | Feb 2016 | B2 |
| 9618488 | Bajic | Apr 2017 | B2 |
| 10020177 | Bajic | Jul 2018 | B2 |
| 10068200 | Greving | Sep 2018 | B1 |
| 10535508 | Murray | Jan 2020 | B2 |
| 10571453 | Cooks | Feb 2020 | B2 |
| 10714323 | Cooks | Jul 2020 | B2 |
| 11125657 | Van Berkel | Sep 2021 | B2 |
| 11226309 | Richardson | Jan 2022 | B2 |
| 20060214101 | Takahashi | Sep 2006 | A1 |
| 20090140137 | Hiraoka | Jun 2009 | A1 |
| 20140070088 | Otsuka | Mar 2014 | A1 |
| 20150034821 | Kyogaku | Feb 2015 | A1 |
| 20150318157 | Otsuka | Nov 2015 | A9 |
| 20150355148 | Bajic | Dec 2015 | A1 |
| 20160018361 | Trimpin | Jan 2016 | A1 |
| 20160203968 | Otsuka | Jul 2016 | A1 |
| 20190006163 | Yim | Jan 2019 | A1 |
| 20190164736 | Murray | May 2019 | A1 |
| 20200343084 | Trimpin | Oct 2020 | A1 |
| Entry |
|---|
| Xia0jun Li; et al., “Vibrating Sharp-edge Spray Ionization (VSSI) for voltage-free direct analysis of samples using mass spectrometry”, Rapid Commun Mass Spectrom, published on-line Jul. 11, 2018, pp. 1-9. |
| Banstola, B., Szot, C. W., AP, D. K., & Murray, K. K. (2018). Piezoelectric matrix-assisted ionization. European Journal of Mass Spectrometry (Chichester, England), 25(2), 202-207 (Year: 2018). |
| ThorLabs, “Precision Cover Glasses and Microscope Slides.” Apr. 9, 2016. (retrieved from https://web.archive.org/web/20160409022329/https://www.thorlabs.com/newgrouppage9.cfm?objectgroup_id=9704) (Year: 2016). |
| Number | Date | Country | |
|---|---|---|---|
| 20210082677 A1 | Mar 2021 | US |
| Number | Date | Country | |
|---|---|---|---|
| 62872702 | Jul 2019 | US |
