Name: multi-faceted mass spectrometric investigation of neuropeptides in callinectes sapidus
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This research was supported by National Science Foundation (CHE-1710140 and CHE-2108223) and National Institutes of Health (NIH) through grant R01DK071801. A.P. was supported in part by the NIH Chemistry-Biology Interface Training Grant (T32 GM008505). N.V.Q. was supported in part by the National Institutes of Health, under the Ruth L. Kirschstein National Research Service Award from the National Heart Lung and Blood Institute to the University of Wisconsin-Madison Cardiovascular Research Center (T32 HL007936). L.L. would like to acknowledge NIH grants R56 MH110215, S10RR029531, and S10OD025084, as well as funding support from a Vilas Distinguished Achievement Professorship and Charles Melbourne Johnson Professorship with funding provided by the Wisconsin Alumni Research Foundation and University of Wisconsin-Madison School of Pharmacy.

All tissue sampling described was performed in compliance with the University of Wisconsin-Madison guidelines.
1. LC-ESI-MS analysis of neuropeptides
<ol>
	<li>Neuropeptide extraction and desalting
	<ol>
		<li>Prior to tissue acquisition, prepare acidified methanol (acMeOH) (90:9:1 MeOH:water:acetic acid) as described in16.</li>
		<li>Collect brain tissue from the crustacean17 and use forceps to immediately place one tissue eac...

<ol>
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A. 1360, 217-228 (2014).</li><li>Li, G., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Nanosecond+photochemically+promoted+click+chemistry+for+enhanced+neuropeptide+visualization+and+rapid+protein+labeling.">Nanosecond photochemically promoted click chemistry for enhanced neuropeptide visualization and rapid protein labeling.</a> Nature Communications. 10 (1), 4697 (2019).</li><li>Corbi&#232;re, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Strategies+for+the+Identification+of+Bioactive+Neuropeptides+in+Vertebrates.">Strategies for the Identification of Bioactive Neuropeptides in Vertebrates.</a> Frontiers in Neuroscience. 13, 948 (2019).</li><li>Chen, R., Ma, M., Hui, L., Zhang, J., Li, L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Measurement+of+neuropeptides+in+crustacean+hemolymph+via+MALDI+mass+spectrometry.">Measurement of neuropeptides in crustacean hemolymph via MALDI mass spectrometry.</a> Journal of American Society for Mass Spectrometry. 20 (4), 708-718 (2009).</li><li>Fridjonsdottir, E., Nilsson, A., Wadensten, H., Andr&#233;n, P. 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The accurate identification, quantification, and localization of neuropeptides and endogenous peptides found in the nervous system are crucial toward understanding their function23,24. Mass spectrometry is a powerful technique that can allow all of this to be accomplished, even in organisms without a fully sequenced genome. The ability of this protocol to detect, quantify, and localize neuropeptides from tissue collected from C. sapidus through a combina...

The nervous system is complex and requires a network of neurons to transmit signals throughout an organism. The nervous system coordinates sensory information and biological response. The intricate and convoluted interactions involved in signal transmission require many different signaling molecules such as neurotransmitters, steroids, and neuropeptides. As neuropeptides are the most diverse and potent signaling molecules that play key roles in activating physiological responses to stress and other stimuli, it is of interest to determine their specific role in these physiological processes. Neuropeptide function is related to their amino acid structure, which determines mobility, receptor interaction, and affinity1. Techniques such as histochemistry, which is important because neuropeptides can be synthesized, stored, and released in different regions of the tissue, and electrophysiology have been employed to investigate neuropeptide structure and function2,3,4, but these methods are limited by throughput and specificity to resolve the vast sequence diversity of neuropeptides.
Mass spectrometry (MS) enables the high throughput analysis of neuropeptide structure and abundance. This can be performed through different MS techniques, most commonly liquid chromatography-electrospray ionization MS (LC-ESI-MS)5 and matrix-assisted laser desorption/ionization MS (MALDI-MS)6. Utilizing high accuracy mass measurements and MS fragmentation, MS provides the ability to assign amino acid sequence and post-translational modification (PTM) status to neuropeptides from complex mixtures without a priori knowledge to aid in ascertaining their function7,8. In addition to qualitative information, MS enables quantitative information of neuropeptides through label-free quantitation (LFQ) or label-based methods such as isotopic or isobaric labeling9. The main advantages of LFQ include its simplicity, low cost of analysis, and decreased sample preparation steps which can minimize sample loss. However, the disadvantages of LFQ include increased instrument time costs as it requires multiple technical replicates to address quantitative error from run-to-run variability. This also leads to a decreased ability to accurately quantify small variations. Label-based methods are subjected to less systematic variation as multiple samples can be differentially labeled using a variety of stable isotopes, combined into one sample, and analyzed through mass spectrometry simultaneously. This also increases throughput, although isotopic labels can be time consuming and costly to synthesize or purchase. Full scan mass spectra (MS1) spectral complexity also increases as multiplexing increases, which decreases the number of unique neuropeptides able to be fragmented and therefore, identified. Conversely, isobaric labeling does not increase spectral complexity at the MS1 level, although it introduces challenges for low abundance analytes such as neuropeptides. As isobaric quantitation is performed at the fragment ion mass spectra (MS2) level, low-abundance neuropeptides may be unable to be quantified as more abundant matrix components may be selected for fragmentation and those selected may not have high enough abundance to be quantified. With isotopic labeling, quantitation can be performed on every identified peptide.
In addition to identification and quantification, localization information can be obtained by MS through MALDI-MS imaging (MALDI-MSI)10. By rastering a laser across a sample surface, MS spectra can be compiled into a heat map image for each m/z value. Mapping transient neuropeptide signal intensity in different regions across conditions can provide valuable information for function determination11. Localization of neuropeptides is especially important because neuropeptide function may differ depending on location12.
Neuropeptides are found in lower abundance in vivo than other signaling molecules, such as neurotransmitters, and thus require sensitive methods for detection13. This can be achieved through the removal of higher abundance matrix components, such as lipids11,14. Additional considerations for the analysis of neuropeptides need to be made when compared to common proteomics workflows, mainly because most neuropeptidomic analyses omit enzymatic digestion. This limits software options for neuropeptide data analysis as most were built with algorithms based on proteomics data and protein matches informed by peptide detection. However, many software such as PEAKS15 is more suited to neuropeptide analysis due to their de novo sequencing capabilities. Several factors need to be considered for the analysis of neuropeptides starting from extraction method to MS data analysis.
The protocols described here include methods for sample preparation and dimethyl isotopic labeling, data acquisition, and data analysis of neuropeptides by LC-ESI-MS, MALDI-MS, and MALDI-MSI. Through representative results from several experiments, the utility and ability of these methods to identify, quantify, and localize neuropeptides from blue crabs, Callinectes sapidus, is demonstrated. To better understand the nervous system, model systems are commonly used. Many organisms do not have a fully sequenced genome available, which prevents comprehensive neuropeptide discovery at the peptide level. In order to mitigate this challenge, a protocol for identifying novel neuropeptides and transcriptome mining to generate databases for organisms without complete genome information is included. All protocols presented here can be optimized for neuropeptide samples from any species, as well as applied for the analysis of any endogenous peptides.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Chemicals, Reagents, and Consumables</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>2,5-Dihydroxybenzoic acid (DHB) matrix</td>
			<td>Supelco</td>
			<td>39319</td>
			<td></td>
		</tr>
		<tr>
			<td>Acetic acid</td>
			<td>Fisher Chemical</td>
			<td>A38S-500</td>
			<td></td>
		</tr>
		<tr>
			<td>Acetonitrile Optima LC/MS grade</td>
			<td>Fisher Chemical</td>
			<td>A955-500</td>
			<td></td>
		</tr>
		<tr>
			<td>Ammonium bicarbonate</td>
			<td>Sigma-Aldrich</td>
			<td>9830</td>
			<td></td>
		</tr>
		<tr>
			<td>Borane pyridine</td>
			<td>Sigma-Aldrich</td>
			<td>179752</td>
			<td></td>
		</tr>
		<tr>
			<td>Bruker peptide calibration mix</td>
			<td>Bruker Daltonics</td>
			<td>NC9846988</td>
			<td></td>
		</tr>
		<tr>
			<td>Capillary</td>
			<td>Polymicro</td>
			<td>1068150019</td>
			<td>to make nanoflow column (75 &#181;m inner diameter x 360 &#181;m outer diameter)</td>
		</tr>
		<tr>
			<td>Cryostat cup</td>
			<td>Sigma-Aldrich</td>
			<td>E6032</td>
			<td>any cup or mold should work</td>
		</tr>
		<tr>
			<td>&#160;Microcentrifuge Tubes</td>
			<td>Eppendorf</td>
			<td>30108434</td>
			<td></td>
		</tr>
		<tr>
			<td>Formaldehyde</td>
			<td>Sigma-Aldrich</td>
			<td>252549</td>
			<td></td>
		</tr>
		<tr>
			<td>Formaldehyde - D2</td>
			<td>Sigma-Aldrich</td>
			<td>492620</td>
			<td></td>
		</tr>
		<tr>
			<td>Formic acid Optima LC/MS grade</td>
			<td>Fisher Chemical</td>
			<td>A117-50</td>
			<td></td>
		</tr>
		<tr>
			<td>Gelatin</td>
			<td>Difco</td>
			<td>214340</td>
			<td>place in 37 &#176;C water bath to melt</td>
		</tr>
		<tr>
			<td>Hydrophobic barrier pen</td>
			<td>Vector Labs</td>
			<td>15553953</td>
			<td></td>
		</tr>
		<tr>
			<td>Indium tin oxide (ITO)-coated glass slides</td>
			<td>Delta Technologies</td>
			<td>CB-90IN-S107</td>
			<td>25 mm x 75 mm x 0.8 mm (width x length x thickness)</td>
		</tr>
		<tr>
			<td>LC-MS vials</td>
			<td>Thermo</td>
			<td>TFMSCERT5000-30LVW</td>
			<td></td>
		</tr>
		<tr>
			<td>Methanol Optima LC/MS Grade</td>
			<td>Fisher Chemical</td>
			<td>A456-500</td>
			<td></td>
		</tr>
		<tr>
			<td>Parafilm</td>
			<td>Sigma-Aldrich</td>
			<td>P7793</td>
			<td>Hydrophobic film</td>
		</tr>
		<tr>
			<td>pH-Indicator strips</td>
			<td>Supelco</td>
			<td>109450</td>
			<td></td>
		</tr>
		<tr>
			<td>Red phosphorus clusters</td>
			<td>Sigma-Aldrich</td>
			<td>343242</td>
			<td></td>
		</tr>
		<tr>
			<td>Reversed phase C18 material</td>
			<td>Waters</td>
			<td>186002350</td>
			<td>manually packed into nanoflow column</td>
		</tr>
		<tr>
			<td>Wite-out pen</td>
			<td>BIC</td>
			<td>150810</td>
			<td></td>
		</tr>
		<tr>
			<td>ZipTip</td>
			<td>Millipore</td>
			<td>Z720070</td>
			<td></td>
		</tr>
		<tr>
			<td>Instruments and Tools</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Automatic matrix sprayer system- M5</td>
			<td>HTX Technologies, LLC</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Centrifuge - 5424 R</td>
			<td>Eppendorf</td>
			<td>05-401-205</td>
			<td></td>
		</tr>
		<tr>
			<td>Cryostat- HM 550</td>
			<td>Thermo Fisher Scientific</td>
			<td>956564A</td>
			<td></td>
		</tr>
		<tr>
			<td>Desiccant</td>
			<td>Drierite</td>
			<td>2088701</td>
			<td></td>
		</tr>
		<tr>
			<td>Forceps</td>
			<td>WPI</td>
			<td>501764</td>
			<td></td>
		</tr>
		<tr>
			<td>MALDI stainless steel target plate</td>
			<td>Bruker Daltonics</td>
			<td>8280781</td>
			<td></td>
		</tr>
		<tr>
			<td>Pipet-Lite XLS</td>
			<td>Rainin</td>
			<td>17014391</td>
			<td>200 &#181;L</td>
		</tr>
		<tr>
			<td>Q Exactive Plus Hybrid Quadrupole-Orbitrap</td>
			<td>Thermo Fisher Scientific</td>
			<td>IQLAAEGAAPFALGMBDK</td>
			<td></td>
		</tr>
		<tr>
			<td>RapifleX MALDI-TOF/TOF</td>
			<td>Bruker Daltonics</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>SpeedVac - SVC100</td>
			<td>Savant</td>
			<td>SVC-100D</td>
			<td></td>
		</tr>
		<tr>
			<td>Ultrasonic Cleaner</td>
			<td>Bransonic</td>
			<td>2510R-MTH</td>
			<td>for sonication</td>
		</tr>
		<tr>
			<td>Ultrasonic homogenizer</td>
			<td>Fisher Scientific</td>
			<td>FB120110</td>
			<td>FB120 Sonic Dismembrator with CL-18 Probe</td>
		</tr>
		<tr>
			<td>Vaccum pump- Alcatel 2008 A</td>
			<td>Ideal Vacuum Products</td>
			<td>P10976</td>
			<td>ultimate pressure = 1 x 10-4 Torr</td>
		</tr>
		<tr>
			<td>Vortex Mixer</td>
			<td>Corning</td>
			<td>6775</td>
			<td></td>
		</tr>
		<tr>
			<td>Water bath (37C) - Isotemp 110</td>
			<td>Fisher Scientific</td>
			<td>15-460-10</td>
			<td></td>
		</tr>
		<tr>
			<td>Data Analysis Software</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Expasy</td>
			<td>https://web.expasy.org/translate/</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>FlexAnalysis</td>
			<td>Bruker Daltonics</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>FlexControl</td>
			<td>Bruker Daltonics</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>FlexImaging</td>
			<td>Bruker Daltonics</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>PEAKS Studio</td>
			<td>Bioinformatics Solutions, Inc.</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>SCiLS Lab</td>
			<td>https://scils.de/</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>SignalP 5.0</td>
			<td>https://services.healthtech.dtu.dk/service.php?SignalP-5.0</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>tBLASTn</td>
			<td>http://blast.ncbi.nlm.nih.gov/Blast.cgi?PROGRAM=tblastn&#38;BLAST_ 
			PROGRAMS=tblastn&#38;PAGE_ 
			TYPE=BlastSearch&#38;SHOW_ 
			DEFAULTS=on&#38;LINK_LOC 
			=blasthome</td>
			<td></td>
			<td></td>
		</tr>
	</tbody>
</table>

multi-faceted mass spectrometric investigation of neuropeptides in callinectes sapidus

Neuropeptides are signaling molecules that regulate almost all physiological and behavioral processes, such as development, reproduction, food intake, and response to external stressors. Yet, the biochemical mechanisms and full complement of neuropeptides and their functional roles remain poorly understood. Characterization of these endogenous peptides is hindered by the immense diversity within this class of signaling molecules. Additionally, neuropeptides are bioactive at concentrations 100x - 1000x lower than that of neurotransmitters and are prone to enzymatic degradation after synaptic release. Mass spectrometry (MS) is a highly sensitive analytical tool that can identify, quantify, and localize analytes without comprehensive a priori knowledge. It is well-suited for globally profiling neuropeptides and aiding in the discovery of novel peptides. Due to the low abundance and high chemical diversity of this class of peptides, several sample preparation methods, MS acquisition parameters, and data analysis strategies have been adapted from proteomics techniques to allow optimal neuropeptide characterization. Here, methods are described for isolating neuropeptides from complex biological tissues for sequence characterization, quantitation, and localization using liquid chromatography (LC)-MS and matrix-assisted laser desorption/ionization (MALDI)-MS. A protocol for preparing a neuropeptide database from the blue crab, Callinectes sapidus, an organism without comprehensive genomic information, is included. These workflows can be adapted to study other classes of endogenous peptides in different species using a variety of instruments.

The workflow for sample preparation and MS analysis is depicted in Figure 1. After the dissection of neuronal tissue, homogenization, extraction, and desalting are performed to purify neuropeptide samples. If isotopic label-based quantification is desired, samples are then labeled and desalted once again. The resulting sample is analyzed through LC-MS/MS for neuropeptide identification and quantification.
Neuropeptides identified through the proteomics software sh...

Watch this Scientific Journal Video about Multi-Faceted Mass Spectrometric Investigation of Neuropeptides in Callinectes sapidus at JoVE.com

Multi-Faceted Mass Spectrometric Investigation of Neuropeptides in Callinectes sapidus

Mass spectrometric characterization of neuropeptides provides sequence, quantitation, and localization information. This optimized workflow is not only useful for neuropeptide studies, but also other endogenous peptides. The protocols provided here describe sample preparation, MS acquisition, MS analysis, and database generation of neuropeptides using LC-ESI-MS, MALDI-MS spotting, and MALDI-MS imaging.

Multi-Faceted Mass Spectrometric Investigation of Neuropeptides in Callinectes sapidus

Neuropeptides are signaling molecules that regulate almost all physiological and behavioral processes, such as development, reproduction, food intake, and ...

The analysis of endogenous peptides, which are smaller than most proteins, but larger than many digested peptides is an under examined field. This protocol addresses the scap in mass spectrometry based workflows. Mass spectrometry is highly sensitive and it can be used to target specific neuropeptides of interest or can capture and detect a range of neuropeptides within a sample.The quantitation and localization of neuropeptide expression by mass spectrometry can lead to the development of peptide therapeutics and the discovery of neuropeptide biomarkers for various diseases. To begin the neuropeptide extraction collect brain tissue from the crustacean and using forceps immediately place one tissue each in a 0.6 milliliter tube containing 20 microliters of acidified methanol. Add 150 microliters of acidified methanol to the sample.Set the total Sonic patient time to 24 seconds, pulse time to eight seconds. Pause time to 15 seconds an amplitude to 50%on an ultrasonic homogenizer and homogenize the samples on ice. Centrifuge the sample at four degrees Celsius at 20, 000 GS for 20 minutes.With a pipette transferred the supernatant to a tube and dry it in a vacuum concentrator at approximately 35 degree Celsius. For desalting reconstitute the extracted tissue sample in 20 microliters of 0.1%formic acid. Vortex the solution and sonicate in a room temperature water bath for one minute.Apply 0.5 microliters of sample to a pH strip to confirm that the pH is less than four. Centrifuge at four degree Celsius and 20, 000 GS for 30 seconds. Prepare wetting equilibration wash in illusion solutions.Obtain a 10 microliter desalting tip with C18 resin. Place the desalting tip on a 20 microliter pipette that is set to 15 microliters. Aspirate the tip three times with wetting solution and three times with equi collaboration solution.Aspirate in the sample 10 times followed by washing three times in wash solution discarding each wash. Elute by aspirating 10 times in each of the illusion solutions in order of increasing Acetonitrile. Dry the alluded neuropeptides in a vacuum concentrator.Reconstitute the dried desalted neuropeptides in five microliters of 0.1%formic acid. Vortex the solution and sonicate it in a room temperature water bath for one minute. Briefly centrifuge at 2000 GS.For spotting of neuropeptides and crusta tissues, pipette a three microliter droplet of sample onto a hydrophobic film.Pipette three microliters of DHB matrix directly on the sample droplet. Mix the solutions by pipetting up and down. Pipette one microliter of the sample and matrix mixture into a well of the MALDI stainless steel target plate and use the pipette tip to spread each mixture out to the edges of the sample well.Spot one microliter of one-to-one caliber and matrix mixture into a well near the sample. Insert target plate containing dried sample spots into MALDI tandem time-of-flight instrument. With the DHB matrix set laser power to 95%Select automatic optimal detector gain and smart complete sample sample carrier movement mode.Acquire MS Spectra in the range of 200 to 3, 200 M over Z and add multiple spectra from each spot together to increase neuropeptide signal to noise ratio. Fill half a cryostat cup with gelatin and allow it to solidify at room temperature. Keep leftover liquid gelatin warm in a 37 degree Celsius water bath.Collect desired neuronal tissue from the animal and use forceps to immediately dip the tissue into a 0.6 milliliter tube containing deionized water for one second. Place the tissue on top of the solid gelatin and fill the rest of the cryostat cup with liquid gelatin. Use forceps to position the tissue.Place the cryostat cup on a flat surface and freeze with dry ice. For sectioning preparation separate the gelatin embedded sample from the cryostat mold by cutting the mold away. Mount the embedded tissue onto a cryostat chuck by pipetting a one milliliter droplet of deionized water onto the chuck and immediately pressing the embedded tissue onto the droplet.Once frozen pipette, more deionized water around the tissue to further secure it to the chuck. Section the tissue at an approximate thickness of one cell. Thumb mount each section onto an Indium tin oxide coated glass slide by placing one side of the slide near the section and placing a finger on the other side of the slide to slowly warm the glass and allow the section to stick to the slide.Export De Novo only peptides. CSV from peaks with an average local confidence score of greater than or equal to 75. Search the peptide list for known sequence motifs indicative of neuropeptides belonging to specific neuropeptide families.Choose a known pre-pro hormone amino acid sequence of interest and use TB blast N to search query pre-pro hormone sequence against a database. Select the target organism and change expect threshold algorithm parameters to 1000 to include low score alignments. Run blast program and then check the results for high homology scores between query and subject sequences producing significant alignments.Save the FASTA file containing nucleotide sequence. Translate pre-pro hormone nucleotide sequence into pre-pro hormone peptide sequences using Expasy translate tool. For callinectes sapidus select invertebrate mitochondrial for genetic code and run the tool.Check for signal peptide sequence and pro hormone cleavage sites in the peptide sequences using signal P.This is a fragmentation spectrum of a neuropeptide identified with 100%sequence coverage in a low fragment mass error with a maximum limit of 0.02 Dalton. Here is a spectrum of a neuropeptide also identified with 100%sequence coverage, but with a low number of fragment ions, therefore the confidence of the identification is low. These are the extracted ion chromatograms for a single neuropeptide that was identified in two separate and consecutive runs.Even though the retention time differs slightly, this can still be used for label free quantification because the time shift is less than one minute. This is an example of a full scan mass spectrum containing a neuropeptide that was Dimethyl labeled resulting in a 4.025 Dalton mass shift between the light and heavy forms of the neuropeptide. The fragment ion mass spectrum of a De Novo sequenced peptide demonstrates good fragmentation coverage, where B and or Y fragment ion was observed for each amino acid with a low mass error of 0.02 Dalton.This indicates that an endogenous peptide belonging to the crustacean RYMI neuropeptide family was observed. Examples of good spots that touch all edges of the well engraving are shown on the left. And examples of bad spots are shown on the right.After MALDI MS imaging of neuropeptides from callinectes sapidus tissues, ion distribution images of various M over Z values were obtained corresponding to different neuropeptides. Extraction solvent optimization for a particular analy type is crucial. Also ensure complete homogenization occurs and adjust the method as needed.Nothing will be detected downstream if it isn't extracted. This technique can provide a foundational list of important neuropeptides that can be further investigated as potential biomarkers, as well as provide untargeted localization information without the need for antibodies.

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Chemistry

Untargeted Metabolomics from Biological Sources Using Ultraperformance Liquid Chromatography-High Resolution Mass Spectrometry (UPLC-HRMS)

Here we present a workflow to analyze the metabolic profiles for biological samples of interest including; cells, serum, or tissue. The sample is first separated into polar and non-polar fractions by a liquid-liquid phase extraction, and partially purified to facilitate downstream analysis. Both aqueous (polar metabolites) and organic (non-polar metabolites) phases of the initial extraction are processed to survey a broad range of metabolites. Metabolites are separated by different liquid chromatography methods based upon their partition properties. In this method, we present microflow ultra-performance (UP)LC methods, but the protocol is scalable to higher flows and lower pressures. Introduction into the mass spectrometer can be through either general or compound optimized source conditions. Detection of a broad range of ions is carried out in full scan mode in both positive and negative mode over a broad m/z range using high resolution on a recently calibrated instrument. Label-free differential analysis is carried out on bioinformatics platforms. Applications of this approach include metabolic pathway screening, biomarker discovery, and drug development.

Untargeted Metabolomics from Biological Sources Using Ultraperformance Liquid Chromatography-High Resolution Mass Spectrometry UPLC-HRMS

Untargeted metabolomics provides a hypothesis generating snapshot of a metabolic profile. This protocol will demonstrate the extraction and analysis of metabolites from cells, serum, or tissue. A range of metabolites are surveyed using liquid-liquid phase extraction, microflow ultraperformance liquid chromatography/high-resolution mass spectrometry (UPLC-HRMS) coupled to differential analysis software.

Here we present a workflow to analyze the metabolic profiles for biological samples of interest including; cells, serum, or tissue. The sample is first ...

Matrix-assisted Laser Desorption/Ionization Time of Flight (MALDI-TOF) Mass Spectrometric Analysis of Intact Proteins Larger than 100 kDa

Effectively determining masses of proteins is critical to many biological studies (e.g. for structural biology investigations). Accurate mass determination allows one to evaluate the correctness of protein primary sequences, the presence of mutations and/or post-translational modifications, the possible protein degradation, the sample homogeneity, and the degree of isotope incorporation in case of labelling (e.g. 13C labelling).
Electrospray ionization (ESI) mass spectrometry (MS) is widely used for mass determination of denatured proteins, but its efficiency is affected by the composition of the sample buffer. In particular, the presence of salts, detergents, and contaminants severely undermines the effectiveness of protein analysis by ESI-MS. Matrix-assisted laser desorption/ionization (MALDI) MS is an attractive alternative, due to its salt tolerance and the simplicity of data acquisition and interpretation. Moreover, the mass determination of large heterogeneous proteins (bigger than 100 kDa) is easier by MALDI-MS due to the absence of overlapping high charge state distributions which are present in ESI spectra.
Here we present an accessible approach for analyzing proteins larger than 100 kDa by MALDI-time of flight (TOF). We illustrate the advantages of using a mixture of two matrices (i.e. 2,5-dihydroxybenzoic acid and &#945;-cyano-4-hydroxycinnamic acid) and the utility of the thin layer method as approach for sample deposition. We also discuss the critical role of the matrix and solvent purity, of the standards used for calibration, of the laser energy, and of the acquisition time. Overall, we provide information necessary to a novice for analyzing intact proteins larger than 100 kDa by MALDI-MS.

Matrix-assisted Laser Desorption/Ionization Time of Flight MALDI-TOF Mass Spectrometric Analysis of Intact Proteins Larger than 100 kDa

Accurate mass measurement represents an important step during the investigation of proteins. Matrix-assisted laser desorption/ionization (MALDI) mass spectrometry (MS) can be used for such determination and its key advantage is the tolerance to salts, detergents and contaminants. Here we illustrate an accessible approach for the analysis of proteins larger than 100 kDa by MALDI-MS.

Effectively determining masses of proteins is critical to many biological studies (e.g. for structural biology investigations). Accurate mass ...

Mass Spectrometric Approaches to Study Protein Structure and Interactions in Lyophilized Powders

Amide hydrogen/deuterium exchange (ssHDX-MS) and side-chain photolytic labeling (ssPL-MS) followed by mass spectrometric analysis can be valuable for characterizing lyophilized formulations of protein therapeutics. Labeling followed by suitable proteolytic digestion allows the protein structure and interactions to be mapped with peptide-level resolution. Since the protein structural elements are stabilized by a network of chemical bonds from the main-chains and side-chains of amino acids, specific labeling of atoms in the amino acid residues provides insight into the structure and conformation of the protein. In contrast to routine methods used to study proteins in lyophilized solids (e.g., FTIR), ssHDX-MS and ssPL-MS provide quantitative and site-specific information. The extent of deuterium incorporation and kinetic parameters can be related to rapidly and slowly exchanging amide pools (Nfast, Nslow) and directly reflects the degree of protein folding and structure in lyophilized formulations. Stable photolytic labeling does not undergo back-exchange, an advantage over ssHDX-MS. Here, we provide detailed protocols for both ssHDX-MS and ssPL-MS, using myoglobin (Mb) as a model protein in lyophilized formulations containing either trehalose or sorbitol.

Here, we present detailed protocols for solid-state amide hydrogen/deuterium exchange mass spectrometry (ssHDX-MS) and solid-state photolytic labeling mass spectrometry (ssPL-MS) for proteins in solid powders. The methods provide high-resolution information on protein conformation and interactions in the amorphous solid-state, which may be useful in formulation design.

Amide hydrogen/deuterium exchange (ssHDX-MS) and side-chain photolytic labeling (ssPL-MS) followed by mass spectrometric analysis can be valuable for ...

Sequencing of Plant Wall Heteroxylans Using Enzymic, Chemical (Methylation) and Physical (Mass Spectrometry, Nuclear Magnetic Resonance) Techniques

This protocol describes the specific techniques used for the characterization of reducing end (RE) and internal region glycosyl sequence(s) of heteroxylans. De-starched wheat endosperm cell walls were isolated as an alcohol-insoluble residue (AIR)1 and sequentially extracted with water (W-sol Fr) and 1 M KOH containing 1% NaBH4 (KOH-sol Fr) as described by Ratnayake et al. (2014)2. Two different approaches (see summary in Figure 1) are adopted. In the first, intact W-sol AXs are treated with 2AB to tag the original RE backbone chain sugar residue and then treated with an endoxylanase to generate a mixture of 2AB-labelled RE and internal region reducing oligosaccharides, respectively. In a second approach, the KOH-sol Fr is hydrolyzed with endoxylanase to first generate a mixture of oligosaccharides which are subsequently labelled with 2AB. The enzymically released ((un)tagged) oligosaccharides from both W- and KOH-sol Frs are then methylated and the detailed structural analysis of both the native and methylated oligosaccharides is performed using a combination of MALDI-TOF-MS, RP-HPLC-ESI-QTOF-MS and ESI-MSn. Endoxylanase digested KOH-sol AXs are also characterized by nuclear magnetic resonance (NMR) that also provides information on the anomeric configuration. These techniques can be applied to other classes of polysaccharides using the appropriate endo-hydrolases.

Sequencing of Plant Wall Heteroxylans Using Enzymic, Chemical Methylation and Physical Mass Spectrometry, Nuclear Magnetic Resonance Techniques

This protocol describes the specific techniques used for the structural characterization of reducing end (RE) and internal region glycosyl sequence(s) of heteroxylans by tagging the RE with 2 aminobenzamide prior to enzymatic (endoxylanase) hydrolysis and then analysis of the resultant oligosaccharides using mass spectrometry (MS) and nuclear magnetic resonance (NMR).

This protocol describes the specific techniques used for the characterization of reducing end (RE) and internal region glycosyl sequence(s) of ...

HKUST-1 as a Heterogeneous Catalyst for the Synthesis of Vanillin

Vanillin (4-hydoxy-3-methoxybenzaldehyde) is the main component of the extract of vanilla bean. The natural vanilla scent is a mixture of approximately 200 different odorant compounds in addition to vanillin. The natural extraction of vanillin (from the orchid Vanilla planifolia, Vanilla tahitiensis and Vanilla pompon) represents only 1% of the worldwide production and since this process is expensive and very long, the rest of the production of vanillin is synthesized. Many biotechnological approaches can be used for the synthesis of vanillin from lignin, phenolic stilbenes, isoeugenol, eugenol, guaicol, etc., with the disadvantage of harming the environment since these processes use strong oxidizing agents and toxic solvents. Thus, eco-friendly alternatives on the production of vanillin are very desirable and thus, under current investigation. Porous coordination polymers (PCPs) are a new class of highly crystalline materials that recently have been used for catalysis. HKUST-1 (Cu3(BTC)2(H2O)3, BTC = 1,3,5-benzene-tricarboxylate) is a very well known PCP which has been extensively studied as a heterogeneous catalyst. Here, we report a synthetic strategy for the production of vanillin by the oxidation of trans-ferulic acid using HKUST-1 as a catalyst.

The conversion of trans-ferulic acid to vanillin was achieved by heterogeneous catalysis. HKUST-1 was employed in this synthesis and the essential step in the catalytic process was the generation of unsaturated metal sites. Thus, when the catalyst was activated under vacuum, full vanillin conversion (yield of 95%) was obtained.

Vanillin (4-hydoxy-3-methoxybenzaldehyde) is the main component of the extract of vanilla bean. The natural vanilla scent is a mixture of approximately ...

Visualization of Ambient Mass Spectrometry with the Use of Schlieren Photography

This manuscript outlines how to visualize mass spectrometry ambient ionization sources using schlieren photography. In order to properly optimize the mass spectrometer, it is necessary to characterize and understand the physical principles of the source. Most commercial ambient ionization sources utilize jets of nitrogen, helium, or atmospheric air to facilitate the ionization of the analyte. As a consequence, schlieren photography can be used to visualize the gas streams by exploiting the differences in refractive index between the streams and ambient air for visualization in real time. The basic setup requires a camera, mirror, flashlight, and razor blade. When properly configured, a real time image of the source is observed by watching its reflection. This allows for insight into the mechanism of action in the source, and pathways to its optimization can be elucidated. Light is shed on an otherwise invisible situation.

This paper presents a protocol for the visualization of gaseous streams of an ambient ionization source using schlieren photography and mass spectrometry.

This manuscript outlines how to visualize mass spectrometry ambient ionization sources using schlieren photography. In order to properly optimize the mass ...

Synthesis and Mass Spectrometry Analysis of Oligo-peptoids

Peptoids are sequence-controlled peptide-mimicking oligomers consisting of N-alkylated glycine units. Among many potential applications, peptoids have been thought of as a type of molecular information storage. Mass spectrometry analysis has been considered the method of choice for sequencing peptoids. Peptoids can be synthesized via solid phase chemistry using a repeating two-step reaction cycle. Here we present a method to manually synthesize oligo-peptoids and to analyze the sequence of the peptoids using tandem mass spectrometry (MS/MS) techniques. The sample peptoid is a nonamer consisting of alternating N-(2-methyloxyethyl)glycine (Nme) and N-(2-phenylethyl)glycine (Npe), as well as an N-(2-aminoethyl)glycine (Nae) at the N-terminus. The sequence formula of the peptoid is Ac-Nae-(Npe-Nme)4-NH2, where Ac is the acetyl group. The synthesis takes place in a commercially available solid-phase reaction vessel. The rink amide resin is used as the solid support to yield the peptoid with an amide group at the C-terminus. The resulting peptoid product is subjected to sequence analysis using a triple-quadrupole mass spectrometer coupled to an electrospray ionization source. The MS/MS measurement produces a spectrum of fragment ions resulting from the dissociation of charged peptoid. The fragment ions are sorted out based on the values of their mass-to-charge ratio (m/z). The m/z values of the fragment ions are compared against the nominal masses of theoretically predicted fragment ions, according to the scheme of peptoid fragmentation. The analysis generates a fragmentation pattern of the charged peptoid. The fragmentation pattern is correlated to the monomer sequence of the neutral peptoid. In this regard, MS analysis reads out the sequence information of the peptoids.

A protocol is described for the manual synthesis of oligo-peptoids followed by sequence analysis by mass spectrometry.

Peptoids are sequence-controlled peptide-mimicking oligomers consisting of N-alkylated glycine units. Among many potential applications, peptoids have ...

A Two-Step Pyrolysis-Gas Chromatography Method with Mass Spectrometric Detection for Identification of Tattoo Ink Ingredients and Counterfeit Products

Tattoo inks are complex mixtures of ingredients. Each of them possesses different chemical properties which have to be addressed upon chemical analysis. In this method for two-step pyrolysis online coupled to gas chromatography mass spectrometry (py-GC-MS) volatile compounds are analyzed during a first desorption run. In the second run, the same dried sample is pyrolyzed for analysis of non-volatile compounds such as pigments and polymers. These can be identified by their specific decomposition patterns. Additionally, this method can be used to differentiate original from counterfeit inks. Easy screening methods for data evaluation using the average mass spectra and self-made pyrolysis libraries are applied to speed up substance identification. Using specialized evaluation software for pyrolysis GS-MS data, a fast and reliable comparison of the full chromatogram can be achieved. Since GC-MS is used as separation technique, the method is limited to volatile substances upon desorption and after pyrolysis of the sample. The method can be applied for quick substance screening in market control surveys since it requires no sample preparation steps.

This method for two-step pyrolysis online coupled to gas chromatography with mass spectrometric detection and data evaluation protocol can be used for multi-component analysis of tattoo inks and discrimination of counterfeit products.

Tattoo inks are complex mixtures of ingredients. Each of them possesses different chemical properties which have to be addressed upon chemical analysis. ...

In situ FTIR Spectroscopy as a Tool for Investigation of Gas/Solid Interaction: Water-Enhanced CO2 Adsorption in UiO-66 Metal-Organic Framework

In situ infrared spectroscopy is an inexpensive, highly sensitive, and selective valuable tool to investigate the interaction of polycrystalline solids with adsorbates. Vibrational spectra provide information on the chemical nature of adsorbed species and their structure. Thus, they are very useful for obtaining molecular level understanding of surface species. The IR spectrum of the sample itself gives some direct information about the material. General conclusions can be drawn concerning hydroxyl groups, some stable surface species and impurities. However, the spectrum of the sample is &#34;blind&#34; with respect to the presence of coordinatively unsaturated ions and gives rather poor information about the acidity of surface hydroxyls, species decisive for the adsorption and catalytic properties of the materials. Furthermore, no discrimination between bulk and surface species can be made. These problems are solved by the use of probe molecules, substances that interact specifically with the surface; the alteration of some spectral features of these molecules as a result of adsorption provides valuable information about the nature, properties, location, concentration, etc., of the surface sites.
The experimental protocol for in-situ IR studies of gas/sample interaction includes preparation of a sample pellet, activation of the material, initial spectral characterization through the analysis of the background spectra, characterization by probe molecules, and study of the interaction with a particular set of gas mixtures. In this paper we investigate a zirconium terephthalate metal organic framework, Zr6O4(OH)4(BDC)6 (BDC = benzene-1,4-dicarboxylate), namely UiO-66 (UiO refers to University of Oslo). The acid sites of the UiO-66 sample are determined by using CO and CD3CN as molecular probes. Furthermore, we have demonstrated that CO2 is adsorbed on basic sites exposed on dehydroxylated UiO-66. Introduction of water to the system produces hydroxyl groups acting as additional CO2 adsorption sites. As a result, CO2 adsorption capacity of the sample is strongly enhanced.

In situ FTIR Spectroscopy as a Tool for Investigation of Gas/Solid Interaction: Water-Enhanced CO2 Adsorption in UiO-66 Metal-Organic Framework

The use of FTIR spectroscopy for investigation of the surface properties of polycrystalline solids is described. Preparation of sample pellets, activation procedures, characterization with probe molecules and model studies of CO2 adsorption are discussed.

In situ infrared spectroscopy is an inexpensive, highly sensitive, and selective valuable tool to investigate the interaction of polycrystalline solids ...

Cell-Lineage Guided Mass Spectrometry Proteomics in the Developing (Frog) Embryo

Characterization of molecular events as cells give rise to tissues and organs raises a potential to better understand normal development and design efficient remedies for diseases. Technologies enabling accurate identification and quantification of diverse types and large numbers of proteins would provide still missing information on molecular mechanisms orchestrating tissue and organism development in space and time. Here, we present a mass spectrometry-based protocol that enables the measurement of thousands of proteins in identified cell lineages in Xenopus laevis (frog) embryos. The approach builds on reproducible cell-fate maps and established methods to identify, fluorescently label, track, and sample cells and their progeny (clones) from this model of vertebrate development. After collecting cellular contents using microsampling or isolating cells by dissection or fluorescence-activated cell sorting, proteins are extracted and processed for bottom-up proteomic analysis. Liquid chromatography and capillary electrophoresis are used to provide scalable separation for protein detection and quantification with high-resolution mass spectrometry (HRMS). Representative examples are provided for the proteomic characterization of neural-tissue fated cells. Cell-lineage-guided HRMS proteomics is adaptable to different tissues and organisms. It is sufficiently sensitive, specific, and quantitative to peer into the spatio-temporal dynamics of the proteome during vertebrate development.

Cell-Lineage Guided Mass Spectrometry Proteomics in the Developing Frog Embryo

Here we describe a mass spectrometry-based proteomic characterization of cell lineages with known tissue fates in the vertebrate Xenopus laevis embryo.

Characterization of molecular events as cells give rise to tissues and organs raises a potential to better understand normal development and design ...