Name: synthesis and mass spectrometry analysis of oligo-peptoids
Uploaded: 2018-02-21T13:00:00.000+00:00
Duration: 11 min 44 s
Description: Watch this Scientific Journal Video about Synthesis and Mass Spectrometry Analysis of Oligo-peptoids at JoVE.com

The authors would like to thank Mr. Michael Connolly and Dr. Ronald Zuckermann (The Molecular Foundry, Lawrence Berkeley National Laboratory) for technique support in peptoid synthesis. We acknowledge the support from the National Science Foundation (CHE-1301505). All mass spectrometry experiments were conducted at the Chemistry Mass Spectrometry Facility at the University of the Pacific.

1. Synthesis of Peptoid
NOTE: The synthesis begins with activating the resin by swelling the resin and removing the protecting group. This is followed by growing the peptoid chain onto the resin through repeating monomer addition cycles. The first monomer coupled to the resin is the C-terminal residue. The peptoid is elongated from the C-terminus to the N-terminus. Once the desired peptoid sequence is achieved, the resin is cleaved off and the peptoid product is purified.
<ol>
	<li>Preparation of reagents 
	NOTE: The liquid reagents are measured using a micropipette and the solid reagents are measured using an analytical balance.
	<ol>
		<li>Mix 6.2 mL of N, N&#39;-diisopropylcarbodiimide (DIC) and 43.8 mL of N,N-dimethylformamide (DMF) to prepare a 0.8 M of DIC/DMF solution.</li>
		<li>Dissolve 5.56 g of BMA into 50.0 mL of DMF to prepare a 0.8 M BMA/DMF solution.</li>
		<li>Mix 2 mL of piperidine (Pip) and 8 mL of DMF to achieve 20% Pip/DMF solution.</li>
		<li>Dissolve 1.9 mL of Npe into 13.1 mL of DMF to achieve 1.0 M Npe/DMF.</li>
		<li>Dissolve 1.3 mL of Nme into 13.7 mL DMF to achieve 1.0 M Nme/DMF.</li>
		<li>Dissolve 0.32 mL&#160;of Nae into 2 mL of DMF to achieve 1.0 M Nae/DMF. 
		Caution: Most of the chemicals used in the synthesis are hazardous. Trifluoroacetic acid (TFA), DIC, Pip, and BMA are hazardous to the skin, eyes, and respiratory tract. DMF and dichloromethane (DCM) are suspected carcinogens. All reactions should be performed in a fume hood and appropriate personal protective equipment should be used. Please check the material safety data sheet (MSDS) of all chemicals used in the synthesis.</li>
	</ol>
	</li>
	<li>Resin activation
	<ol>
		<li>Measure out 84 mg of Rink amide resin (Resin, 0.047 mmol, loading 0.56 mmol/g) and add it to a 10 mL polypropylene solid-phase reaction vessel. Insert the plunger into the vessel.</li>
		<li>Add 2 mL of DMF to the reaction vessel and cap the vessel with a pressure cap. Place the vessel on a shaker, and agitate the vessel at room temperature at an angle of movement of approximately 12 degrees and 385 oscillations/min for 30 min. Drain the solution to a waste container by removing the cap and pushing the plunger of the reaction vessel.</li>
		<li>Add 2 mL of 20% Pip/DMF solution to the vessel and cap the vessel. Agitate it on the shaker for 2 min, and drain the solution to the waste container.</li>
		<li>Add 2 mL of 20% Pip/DMF solution to the vessel, cap the vessel, and agitate it at room temperature for 12 min. Remove the cap and drain the solution to the waste container.</li>
		<li>Wash the resin by adding 1 mL of DMF, capping the vessel, and agitating the vessel for 1 min. Remove the cap and drain the solution by pushing the plunger. Wash the Resin with DMF for 4 additional times.</li>
	</ol>
	</li>
	<li>Monomer addition and N-terminal acetylation 
	NOTE: Each monomer addition cycle involves two reaction steps, bromoacetylation and displacement.
	<ol>
		<li>Carry out the first monomer addition cycle to form Nme-Resin.</li>
		<li>Perform a bromoacetylation reaction. Mix 1 mL of 0.8 M BMA/DMF solution and 1 mL of 0.8 M DIC/DMF solution in a beaker. Transfer the mixture to a reaction vessel containing Resin and cap the vessel. Place the vessel on the shaker and agitate it at room temperature for 20 min. Remove the cap and drain the solution to the waste container.</li>
		<li>Wash the resin by adding 1 mL of DMF, capping the vessel, agitating it for 1 min, and draining the solution by pushing the plunger. Wash the resin by adding 1 mL of DCM, agitating the vessel for 1 min, and draining the solution. Wash the resin with DCM once more, and then wash it with DMF twice.</li>
		<li>Perform a displacement reaction. Add 1 mL of 1.0 M Nme/DMF solution, cap the vessel, agitate the vessel at room temperature for 60 min. Remove the cap and drain the solution by pushing the plunger.</li>
		<li>Wash the resin by adding 1 mL DMF, agitating the vessel for 1 min, and draining the solution by pushing the plunger. Wash the resin by drawing in 1 mL DCM, agitating for 1 min, and draining the solution. Wash DCM once more, followed by washing with DMF twice.</li>
		<li>Repeat monomer addition cycles from steps 1.3.2 to 1.3.5 to form Nae-(Npe-Nme)4-resin. When repeating the step of displacement reaction (1.3.4), use a specific amine solution according to the peptoid sequence. 
		NOTE: The peptoid chain is elongated from the C-terminus to the N-terminus with the C-terminal residue bound to the Resin.</li>
		<li>Perform N-terminal acetylation to form Ac-Nae-(Npe-Nme)4-resin.</li>
		<li>Mix 92 &#181;L of acetic anhydride, 43.5 &#181;L of N,N-diisopropylethylamine (DIPEA), and 2 mL of DMF in a beaker to make about 2 mL of acetylation cocktail.</li>
		<li>Add 2 mL of acetylation cocktail to the vessel containing resin, cap the vessel, and agitate it at room temperature for 60 min. Remove the cap and drain the solution by pushing the plunger.</li>
		<li>Wash the resin by adding 1 mL of DMF, agitating the vessel for 1 min, and draining the solution by pushing the plunger. Wash the resin by adding 1 mL of DCM, agitating the vessel for 1 min, and draining the solution. Repeat washing the resin with DCM once more, then wash with DMF twice more.</li>
		<li>Wash the resin by adding 1 mL of DCM, agitating the vessel for 1 min, and draining the solution by pushing the plunger. Repeat washing with DCM twice. Remove the cap and let the resin air-dry in the reaction vessel for 10 min.</li>
	</ol>
	</li>
	<li>Cleavage and purification
	<ol>
		<li>Mix 3.8 mL of TFA, 100 &#181;L of triisopropylsilane (TIPS), and 100 &#181;L of HPLC-grade H2O in a beaker to make 4 mL of cleavage cocktail.</li>
		<li>Add 4 mL of freshly made cleavage cocktail to the vessel containing resin, cap the vessel, and agitate it at room temperature for 2 h.</li>
		<li>Remove the cap and collect the filtrate solution into a 50 mL polypropylene centrifuge tube. Add 1 mL of TFA to the vessel, cap it, and agitate for 1 min. Collect the filtrate solution into the same centrifuge tube.</li>
		<li>Evaporate TFA by blowing in a stream of nitrogen gas gently until about 1 mL viscous solution is left.</li>
		<li>Add 15 mL of diethyl ether to the remaining solution, cap the centrifuge tube, and incubate it in a -20 &#176;C freezer for 2 h to overnight. The crude peptoid&#160;precipitates as white solid.</li>
		<li>Pellet the solid using a centrifuge at 4,427 x g for 10 min. Remove the cap of the centrifuge tube and decant diethyl ether into a beaker carefully without losing the solid. 
		Caution: Diethyl ether is a flammable organic solvent. Please use a diethyl ether safe centrifuge.</li>
		<li>Wash the solid by adding 10 mL of ice-cold diethyl ether into the centrifuge tube containing the solid, capping the tube, and placing it in the centrifuge. Perform centrifugation at 4,427 x g for 10 min. Remove the centrifuge tube from the centrifuge and decant diethyl ether into a beaker carefully without losing the solid.</li>
		<li>Dry the solid by gently blowing in a stream of nitrogen gas.</li>
		<li>Add 10 mL of HPLC-grade H2O to dissolve the dried solid. Pass the solution through a nylon syringe filter with pore size of 0.45 &#181;m, and collect the filtrate into a pre-weighted 50 mL polypropylene centrifuge tube.</li>
		<li>Shell freeze the solution by placing and rotating the centrifuge tube containing the peptoid solution in a 12-ounce, double-stacked expanded polystyrene cup 1/3 filled with liquid nitrogen. Lyophilize the frozen solution overnight to yield solid peptoid.</li>
		<li>Repeat lyophilization one more time by dissolving the solid peptoid into 10 mL of HPLC-grade H2O, shell freezing in liquid nitrogen, and lyophilizing overnight. The resulting peptoid is sufficiently pure for sequence analysis by mass spectrometry.</li>
	</ol>
	</li>
</ol>
2. MS Measurements and Sequence Analysis
NOTE: The MS/MS experiment is carried out in a triple-quadrupole mass spectrometer coupled to an electrospray ionization (ESI) source. Data collection is controlled by using the data acquisition software accompanied with the instrument. The general procedure includes 1) performing the full scan mass spectrometry experiment and recording the mass spectrum, 2) performing the CID MS/MS experiment and recording the MS/MS spectrum, and 3) comparing the MS/MS spectral data with theoretical fragmentation scheme predicted based on the structural feature of the peptoid.
<ol>
	<li>Preparation of sample solution
	<ol>
		<li>Weigh out 1.0 - 2.0 mg solid peptoid in a 3 - 5 mL glass vial. Add 1 mL mixed solvent of acetonitrile and water (ACN/H2O, 1:1, v/v) to dissolve the peptoid. This gives the stock sample solution with a concentration of about 10-3 M.</li>
		<li>Transfer 20 &#181;L of stock solution into a 1.5 mL centrifuge tube and add 1 mL mixed solvent of ACN/H2O to yield a diluted sample solution of about 10-5 M.</li>
		<li>Remove any possible insoluble particles in the diluted sample solution by performing centrifugation at 4,427 x g for 3 min. Transfer about 700 &#181;L of the top portion of the solution into another 1.5 mL centrifuge tube to make the peptoid MS working solution with concentration of about 10-5 M.</li>
		<li>Adjust the concentration of the MS working solution based on the observed signal intensity during mass spectrometry measurements.</li>
		<li>An alternative way to remove any possible insoluble particles in the diluted sample solution is to pass the sample solution through a 0.20 &#181;m syringe filter and collect the filtrate into a 1.5 mL centrifuge tube to make the peptoid MS working solution of about 10-5 M.</li>
	</ol>
	</li>
	<li>Recording mass spectra
	<ol>
		<li>Run mixed solvent of ACN/H2O (1:1, v/v) through the electrospray ionization (ESI) source and set up the instrument in a standard positive ion, full scan mass spectrometry mode with a mass-to-charge ratio (m/z) range of 100 - 1500. 
		Note: 
		Typical operating parameters: 
		ESI needle voltage, 5 kV 
		Capillary voltage, 40 V 
		Drying gas (nitrogen gas) temperature, 200 &#176;C.</li>
		<li>Add approximately 300 &#181;L of peptoid MS working solution (about 10-5 M) into a 500 &#181;L or a 1 mL syringe and connect the syringe to the ESI inlet using capillary polyether ether ketone (PEEK) tubing. Place the syringe onto the syringe pump and set the flow rate at 10 &#181;L/min to infuse the sample solution into the ESI inlet.</li>
		<li>Turn on the ESI needle voltage to activate the ESI process, and then turn on the detector. Set the display in profile mode and the m/z range of 100 - 1,500. View a mass spectrum profile shown in the profile window. The peak at m/z 1,265 (displayed as m/z of 1,264.6) corresponds to the peptoid ion or protonated peptoid.</li>
		<li>Record the MS spectrum for 2 min. In the &#34;Method Window&#34;, use 2 min as the &#34;run time.&#34;&#160;Open the recording window and fill in a proper file name, and start to record the spectrum. 
		NOTE: The resulting mass spectrum is shown in Figure 3.</li>
		<li>Optimize the intensity of the peak at m/z of 1,265. Set the m/z range to 1,150 - 1,350 and adjust the capillary voltage while viewing the peak intensity in mV shown in the profile window. For example, increase the capillary voltage to 50 V or higher and view the change of the peak intensity. The optimal peak intensity is around 150 - 200 mV. 
		NOTE: Adjusting the capillary voltage can significantly change the abundance of certain ions. Increasing the capillary voltage may enhance the intensity of the peptoid ion. However, a high capillary voltage may also induce dissociation of the peptoid ion in the ion source, and decrease the observed intensity. Adjusting the temperature of drying gas may enhance the intensity of the peak at m/z 1,265, but it is less effective than adjusting the capillary voltage. If the peak at m/z 1,265 does not reach the optimal intensity, adjust the sample concentration (or example, double the concentration of the MS working solution).</li>
		<li>Switch the instrument to the MS/MS mode. Set the precursor ion at m/z 1,265 and the MS/MS mass range at m/z of 100 - 1,400. In the &#34;Method Window,&#34;&#160;use m/z 1,265 as the &#34;Q1 First Mass&#34; and leave the &#34;Q1 Last Mass&#34; blank. Use m/z 100 as the &#34;Q3 First Mass&#34; and m/z 1,400 as the &#34;Q3 Last Mass.&#34; 
		NOTE: In the MS/MS mode, the first quadrupole unit (Q1) functions as a mass filter to isolate the peptoid ion as the precursor ion, the second quadrupole unit (Q2) is a collision cell, and the third quadrupole unit (Q3) functions as a mass analyzer.</li>
		<li>Set the collision energy at 40 eV and the collision gas (argon, in this case) pressure at 1.5 mTorr.</li>
		<li>View a mass spectrum profile displayed in the profile window. The peak at m/z of 1,265 corresponds to the peptoid ion, and the peaks with lower m/z values represent the fragments from the peptoid ion.</li>
		<li>Adjust the collision energy to optimize the display of the fragmentation spectrum. For example, increase the collision energy to 45 eV and view the change of the spectrum profile. 
		NOTE: In general, increasing the collision energy will enhance the abundance of the fragment ions and reduce the abundance of the peptoid ion. Increasing the collision gas pressure will also enhance the abundance of the fragment ions. 
		Caution: Do not increase the collision gas pressure beyond 2 mTorr.</li>
		<li>Record the MS/MS spectrum for 2 min. In the &#34;Method Window,&#34;&#160;use 2 min as the &#34;run time.&#34;&#160;Open the recording window and fill in a proper file name, and start to record the spectrum.</li>
		<li>Repeat recording 1 - 2 times.</li>
	</ol>
	</li>
	<li>Peptoid sequence analysis 
	NOTE: Under the CID condition, the peptoid ion would fragment at the amide bonds along the peptoid backbone to produce a series of N-terminal fragments called B-ions, and a series of C-terminal fragments called Y-ions
	<ol>
		<li>Draw out the chemical structure of the acetylated peptoid by placing the N-terminus on the left side and the C-terminus on the right side, and draw a dashed line at each amide bond to generate a fragmentation scheme as shown in Figure 2a. Draw a proton with a dashed circle to indicate the charge carrier. Starting from the left side of the structure, place labels on the dashed lines to indicate the N-terminal fragments as B1, B2, to B8. Starting from the right side, place labels on the dashed lines to indicate the C-terminal fragments as Y1, Y2, to Y8. 
		NOTE: A chemical drawing software can be utilized to draw the peptoid structure.</li>
		<li>Imagine fragmentation at the 4th amide bond from the left side, and draw the structures of the N-terminal fragment and the C-terminal fragment with proper formal charges, as shown in Figure 2b. Place the label of B4 on the N-terminal fragment, and place the label of Y5 on the C-terminal fragment. Calculate the m/z value of B4 by summing up the nominal masses of the elements in the structure to yield a value of 580, and place m/z 580 on the N-terminal fragment. Calculate the m/z value of Y5 and place m/z 685 on the C-terminal fragment.</li>
		<li>Calculate the m/z values for all eight B ions and all eight Y ions, and assemble them in a table, as shown in Table 1. 
		NOTE: The m/z values of the fragments can be calculated using a chemical drawing software.</li>
		<li>Open the recorded MS/MS spectrum of the peptoid using the data review software accompanied with the instrument. Set the Labeling Preferences to &#34;Show Ion Labels&#34; and Label Threshold to 3%. This generates a MS/MS spectrum with m/z values labeled on the peaks.</li>
		<li>Export the MS/MS spectral data as a text file in the CSV format and reconstruct the spectrum using data processing software. Place m/z values on the peaks. The resulting MS/MS spectrum is shown in Figure 4. 
		NOTE: Some mass spectrometers are equipped with data processing software capable for generating the MS/MS spectrum. In this case, exporting the MS/MS spectral data is not necessary.</li>
		<li>Assign the m/z values shown on the MS/MS spectrum to those shown in Table 1 to identify the corresponding B- and Y-ions. For example, the peak at m/z 580 is identified as the B4-ion and m/z 685 is identified as the Y5-ion. Label the peaks with corresponding B and Y symbols on the spectrum, as shown in Figure 4.</li>
	</ol>
	</li>
</ol>

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Mass Spectrom. 308 (1), 98-108 (2011).</li><li>Bogdanov, B., Zhao, X., Robinson, D. B., Ren, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Electron+Capture+Dissociation+Studies+of+the+Fragmentation+Patterns+of+Doubly+Protonated+and+Mixed+Protonated-Sodiated+Peptoids.">Electron Capture Dissociation Studies of the Fragmentation Patterns of Doubly Protonated and Mixed Protonated-Sodiated Peptoids.</a> J. Am. Soc. Mass Spectrom. 25 (7), 1202-1216 (2014).</li><li>Ren, J., Tian, Y., Hossain, E., Connolly, M. D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Fragmentation+Patterns+and+Mechanisms+of+Singly+and+Doubly+Protonated+Peptoids+Studied+by+Collision+Induced+Dissociation.">Fragmentation Patterns and Mechanisms of Singly and Doubly Protonated Peptoids Studied by Collision Induced Dissociation.</a> J. Am. Soc. Mass Spectrom. 27 (4), 646-661 (2016).</li></ol>

The authors have nothing to disclose.

A nonamer peptoid, Ac-Nae-(Npe-Nme)4-NH2, has been synthesized using the protocol presented. The synthesis apparatus involves a syringe-like polypropylene solid-phase reaction vessel and a mechanical shaker. The reaction vessels are commercially available and low cost. A mechanical shaker is a common apparatus in chemistry laboratories. With the use of a syringe-like reaction vessel, solutions can be drawn into and pushed out of the vessel by manually moving the plunger. This technique allows the mo...

Peptoids are a class of sequence-controlled polymers with backbone structures mimicking the structure of peptides. Peptoids can be synthesized from diverse amines, which enables peptoids to exhibit highly tunable properties1,2. Peptoids have been used as molecular models for biophysical research, considered as therapeutic agents, and designed as ligands for proteins3,4,5,6. Peptoids have been developed into a variety of biologically active compounds, such as anti-fouling and antibody-mimetic materials, antimicrobial agents, and enzyme inhibitors7,8,9. With a highly ordered and tunable nature, peptoids have also been thought of as a type of molecular information storage10. The discovery of these diverse applications calls for the development of efficient analytical methods to characterize the sequence and structure of peptoids. Tandem mass spectrometry-based techniques have shown promise as the method of choice for analyzing the sequence properties of sequence-controlled polymers, including peptoids11,12,13,14,15. However, systematic studies correlating the peptoid ion fragmentation patterns resulting from mass spectrometry studies and the structural information of peptoids are very limited.
Peptoids can be readily synthesized using a solid phase method. The well-developed method involves an iteration of a two-step monomer addition cycle16,17. In each addition cycle, a resin-bound amine is acetylated by a haloacetic acid (typically bromoacetic acid, BMA), and this is followed by a displacement reaction with a primary amine. Although automated synthesis protocols have been routinely applied for peptoid synthesis, peptoids can be synthesized manually with excellent yields in a standard chemistry laboratory16,18,19,20.
Our lab has adopted the method of manual peptoid synthesis and simplified the apparatus used in the existing methods. We have previously studied the fragmentation patterns of a series of peptoids using MS/MS techniques21,22,23. Our results show that peptoids produce characteristic fragmentations when they are subjected to collision-induced dissociation (CID)21,23 or electron-capture dissociation (ECD)22 experiments. In this article, we demonstrate how oligo-peptoids can be synthesized in a standard&#160;chemistry laboratory, how to perform the CID experiments using a triple-quadrupole mass spectrometer, and how to analyze the spectral data. The peptoid to be synthesized and characterized is a nonamer with N-terminal acetylation and C-terminal amidation, Ac-Nae-(Npe-Nme)4-NH2. The structure of the peptoid is shown in Figure 1.

<table><tbody><tr><td>ESI-triple quadrupole mass spectrometer, Varian 320L</td><td>Agilent Technologies Inc.</td><td></td><td>The mass spectrometer was acquired from Varian, Inc.</td></tr><tr><td>Varian MS workstation, Version 6.9.2, a data acquisition and data review software</td><td>Varian Inc.</td><td></td><td>The software is a part of the Varian 320L package</td></tr><tr><td>Burrell Scientific Wrist-action shaker, Model 75 DD</td><td>Fisher Scientific International Inc.</td><td>14-400-126</td><td></td></tr><tr><td>Hermle Centrifuge, Model Z 206 A</td><td>Hermle Labortechnik GmbH</td><td></td><td></td></tr><tr><td>Solid phase reaction vessel, 10 mL</td><td>Torviq</td><td>SF-1000</td><td></td></tr><tr><td>Pressure caps for reaction vessels</td><td>Torviq</td><td>PC-SF</td><td></td></tr><tr><td>Syringe filters, pore size 0.2 &amp;mu;m</td><td>Fisher Scientific Inc.</td><td>03-391-3B</td><td></td></tr><tr><td>Syringe filters, pore size 0.45 &amp;mu;m</td><td>Fisher Scientific Inc.</td><td>03-391-3A</td><td></td></tr><tr><td>Polypropylene centrifuge tuges, 50 mL</td><td>VWR International, LLC.</td><td>490001-626</td><td></td></tr><tr><td>Polypropylene centrifuge tuges, 15 mL</td><td>VWR International, LLC.</td><td>490001-620</td><td></td></tr><tr><td>ChemBioDraw, Ultra, Version 12.0</td><td>CambridgeSoft Corporation</td><td></td><td>CambridgeSoft is now part of PerkinElmer Inc.</td></tr><tr><td>Styrofoam cup, 12 Oz</td><td>Common Supermarket</td><td></td><td></td></tr><tr><td>Rink amide resin</td><td>Chem-Impex International, Inc.</td><td>10619</td><td></td></tr><tr><td>Piperidine</td><td>Chem-Impex International, Inc.</td><td>02351</td><td>Highly toxic</td></tr><tr><td>N, N&amp;rsquo;-diisopropylcarbodiimide</td><td>Chem-Impex International, Inc.</td><td>00110</td><td>Highly toxic</td></tr><tr><td>Bromoacetic acid</td><td>Chem-Impex International, Inc.</td><td>26843</td><td>Highly toxic</td></tr><tr><td>2-Phenylethylamine</td><td>VWR International, LLC.</td><td>EM8.07334.0250</td><td></td></tr><tr><td>2-Methyoxyethylamine</td><td>Sigma-Aldrich Co. LLC.</td><td>241067</td><td></td></tr><tr><td>N-Boc-ethylenediamine</td><td>VWR International, LLC.</td><td>AAAL19947-06</td><td></td></tr><tr><td>Acetic anhydride</td><td>Sigma-Aldrich Co. LLC.</td><td>252845</td><td></td></tr><tr><td>N, N-dimethylformamide</td><td>VWR International, LLC.</td><td>BDH1117-4LG</td><td>Further distillation before use</td></tr><tr><td>N, N-diisopropylethylamine</td><td>Chem-Impex International, Inc.</td><td>00141</td><td></td></tr><tr><td>Triisopropylsilane</td><td>Chem-Impex International, Inc.</td><td>01966</td><td></td></tr><tr><td>Trifluoroacetic acid</td><td>Chem-Impex International, Inc.</td><td>00289</td><td>Highly toxic</td></tr><tr><td>Millipore MILLI-Q Academic Water Purification System</td><td>Millipore Corporation</td><td>ZMQP60001</td><td>For generating HPLC grade water</td></tr><tr><td>HPLC-grade Water</td><td></td><td></td><td>Produced from Millipore MILLI-Q&amp;reg; Academic Water Purification System</td></tr><tr><td>Methanol</td><td>Pharmco-Aaper</td><td>339USP/NF</td><td>HPLC grade</td></tr><tr><td>Acetonitrile</td><td>Fisher Scientific International, Inc.</td><td>A998-4</td><td>HPLC grade</td></tr><tr><td>Diethyl ether</td><td>VWR International, LLC.</td><td>BDH1121-19L</td><td>Further distillation before use</td></tr><tr><td>Dichloromethane</td><td>VWR International, LLC.</td><td>BDH1113-19L</td><td>Further distillation before use</td></tr><tr><td>Nitrogen gas</td><td>Fresno Oxygen/Barnes Supply</td><td>NIT 50-C-F</td><td>Ultra high purity, 99.9995%</td></tr><tr><td>Argon gas</td><td>Fresno Oxygen/Barnes Supply</td><td>ARG 50-C-F</td><td>Ultra high purity, 99.9995%</td></tr></tbody></table>

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.

The structure of a 9-mer peptoid with N-terminal acetylation, Ac-Nae-(Npe-Nme)4-NH2, is shown in Figure 1. The peptoid was synthesized manually in a fritted polypropylene reaction vessel via solid phase approach. Rink amide resin (0.047 mmol, 84 mg with loading 0.56 mmol/g) is used as the solid support to yield the peptoid with an amidated C-terminus. The peptoid chain is built by multiple cycles of monomer addition. Each monomer additio...

Watch this Scientific Journal Video about Synthesis and Mass Spectrometry Analysis of Oligo-peptoids at JoVE.com

Synthesis and Mass Spectrometry Analysis of Oligo-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 ...

synthesis-and-mass-spectrometry-analysis-of-oligo-peptoids

Research

JoVE Journal

Chemistry

10.6K Views.  University of the Pacific. A protocol is described for the manual synthesis of oligo-peptoids followed by sequence analysis by mass spectrometry.

Video: Synthesis and Mass Spectrometry Analysis of Oligo-peptoids

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 ...

Detection of Protein Ubiquitination Sites by Peptide Enrichment and Mass Spectrometry

The posttranslational modification of proteins by the small protein ubiquitin is involved in many cellular events. After tryptic digestion of ubiquitinated proteins, peptides with a diglycine remnant conjugated to the epsilon amino group of lysine (&#39;K-&#949;-diglycine&#39; or simply &#39;diGly&#39;) can be used to track back the original modification site. Efficient immunopurification of diGly peptides combined with sensitive detection by mass spectrometry has resulted in a huge increase in the number of ubiquitination sites identified up to date. We have made several improvements to this workflow, including offline high pH reverse-phase fractionation of peptides prior to the enrichment procedure, and the inclusion of more advanced peptide fragmentation settings in the ion routing multipole. Also, more efficient cleanup of the sample using a filter-based plug in order to retain the antibody beads results in a greater specificity for diGly peptides. These improvements result in the routine detection of more than 23,000 diGly peptides from human cervical cancer cells (HeLa) cell lysates upon proteasome inhibition in the cell. We show the efficacy of this strategy for in-depth analysis of the ubiquitinome profiles of several different cell types and of in vivo samples, such as brain tissue. This study presents an original addition to the toolbox for protein ubiquitination analysis to uncover the deep cellular ubiquitinome.

We present a method for the purification, detection, and identification of diGly peptides that originate from ubiquitinated proteins from complex biological samples. The presented method is reproducible, robust, and outperforms published methods with respect to the level of depth of the ubiquitinome analysis.

The posttranslational modification of proteins by the small protein ubiquitin is involved in many cellular events. After tryptic digestion of ...

Biochemistry

Synthesis and Structure Determination of &#181;-Conotoxin PIIIA Isomers with Different Disulfide Connectivities

Peptides with a high number of cysteines are usually influenced regarding the three-dimensional structure by their disulfide connectivity. It is thus highly important to avoid undesired disulfide bond formation during peptide synthesis, because it may result in a completely different peptide structure, and consequently altered bioactivity. However, the correct formation of multiple disulfide bonds in a peptide is difficult to obtain by using standard self-folding methods such as conventional buffer oxidation protocols, because several disulfide connectivities can be formed. This protocol represents an advanced strategy required for the targeted synthesis of multiple disulfide-bridged peptides which cannot be synthesized via buffer oxidation in high quality and quantity. The study demonstrates the application of a distinct protecting group strategy for the synthesis of all possible 3-disulfide-bonded peptide isomers of &#181;-conotoxin PIIIA in a targeted way. The peptides are prepared by Fmoc-based solid phase peptide synthesis using a protecting group strategy for defined disulfide bond formation. The respective pairs of cysteines are protected with trityl (Trt), acetamidomethyl (Acm), and tert-butyl (tBu) protecting groups to make sure that during every oxidation step only the required cysteines are deprotected and linked. In addition to the targeted synthesis, a combination of several analytical methods is used to clarify the correct folding and generation of the desired peptide structures. The comparison of the different 3-disulfide-bonded isomers indicates the importance of accurate determination and knowledge of the disulfide connectivity for the calculation of the three-dimensional structure and for interpretation of the biological activity of the peptide isomers. The analytical characterization includes the exact disulfide bond elucidation via tandem mass spectrometry (MS/MS) analysis which is performed with partially reduced and alkylated derivatives of the intact peptide isomer produced by an adapted protocol. Furthermore, the peptide structures are determined using 2D nuclear magnetic resonance (NMR) experiments and the knowledge obtained from MS/MS analysis.

Cysteine-rich peptides fold into distinct three-dimensional structures depending on their disulfide connectivity. Targeted synthesis of individual disulfide isomers is required when buffer oxidation does not lead to the desired disulfide connectivity. The protocol deals with the selective synthesis of 3-disulfide-bonded peptides and their structural analysis using NMR and MS/MS studies.

Peptides with a high number of cysteines are usually influenced regarding the three-dimensional structure by their disulfide connectivity. It is thus ...

Semi-Quantitative Analysis of Peptidoglycan by Liquid Chromatography Mass Spectrometry and Bioinformatics

Peptidoglycan is an important component of bacterial cell walls and a common cellular target for antimicrobials. Although aspects of peptidoglycan structure are fairly conserved across all bacteria, there is also considerable variation between Gram-positives/negatives and between species. In addition, there are numerous known variations, modifications, or adaptations to the peptidoglycan that can occur within a bacterial species in response to growth phase and/or environmental stimuli. These variations produce a highly dynamic structure that is known to participate in many cellular functions, including growth/division, antibiotic resistance, and host defense avoidance. To understand the variation within peptidoglycan, the overall structure must be broken down into its constitutive parts (known as muropeptides) and assessed for overall cellular composition. Peptidoglycomics uses advanced mass spectrometry combined with high-powered bioinformatic data analysis to examine peptidoglycan composition in fine detail. The following protocol describes the purification of peptidoglycan from bacterial cultures, the acquisition of muropeptide intensity data through a liquid chromatograph&#8212;mass spectrometer, and the differential analysis of peptidoglycan composition using bioinformatics.

This protocol covers a detailed analysis of peptidoglycan composition using liquid chromatography mass spectrometry coupled with advanced feature extraction and bioinformatic analysis software.

Peptidoglycan is an important component of bacterial cell walls and a common cellular target for antimicrobials. Although aspects of peptidoglycan ...

Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly

This protocol presents the use of Lewis acidic multi-role reagents to circumvent kinetic trapping observed during the self-assembly of information-encoded oligomeric strands mediated by paired dynamic covalent interactions in a manner mimicking the thermal cycling commonly employed for the self-assembly of complementary nucleic acid sequences. Primary amine monomers bearing aldehyde and amine pendant moieties are functionalized with orthogonal protecting groups for use as dynamic covalent reactant pairs. Using a modified automated peptide synthesizer, the primary amine monomers are encoded into oligo(peptoid) strands through solid-phase submonomer synthesis. Upon purification by high-performance liquid chromatography (HPLC) and characterization by electrospray ionization mass spectrometry (ESI-MS), sequence-specific oligomers are subjected to high-loading of a Lewis acidic rare-earth metal triflate which both deprotects the aldehyde moieties and affects the reactant pair equilibrium such that strands completely dissociate. Subsequently, a fraction of the Lewis acid is extracted, enabling annealing of complementary sequence-specific strands to form information-encoded molecular ladders characterized by matrix assisted laser desorption/ionization mass spectrometry (MALDI-MS). The simple procedure outlined in this report circumvents kinetic traps commonly experienced in the field of dynamic covalent assembly and serves as a platform for the future design of robust, complex architectures.

A protocol is presented for the synthesis of information-encoded peptoid oligomers and for the sequence-directed self-assembly of these peptoids into molecular ladders using amines and aldehydes as dynamic covalent reactant pairs and Lewis acidic rare-earth metal triflates as multi-role reagents.

This protocol presents the use of Lewis acidic multi-role reagents to circumvent kinetic trapping observed during the self-assembly of information-encoded ...

Sample Preparation and Relative Quantitation using Reductive Methylation of Amines for Peptidomics Studies

Peptidomics can be defined as the qualitative and quantitative analysis of peptides in a biological sample. Its main applications include identifying the peptide biomarkers of disease or environmental stress, identifying neuropeptides, hormones, and bioactive intracellular peptides, discovering antimicrobial and nutraceutical peptides from protein hydrolysates, and can be used in studies to understand the proteolytic processes. The recent advance in sample preparation, separation methods, mass spectrometry techniques, and computational tools related to protein sequencing has contributed to the increase of the identified peptides number and peptidomes characterized. Peptidomic studies frequently analyze peptides that are naturally generated in cells. Here, a sample preparation protocol based on heat-inactivation is described, which eliminates protease activity, and extraction with mild conditions, so there is no peptide bonds cleavage. In addition, the relative quantitation of peptides using stable isotope labeling by reductive methylation of amines is also shown. This labeling method has some advantages as the reagents are commercially available, inexpensive compared to others, chemically stable, and allows the analysis of up to five samples in a single LC-MS run.

This article describes a sample preparation method based on heat-inactivation to preserve endogenous peptides avoiding degradation post-mortem, followed by relative quantitation using isotopic labeling plus LC-MS.

Peptidomics can be defined as the qualitative and quantitative analysis of peptides in a biological sample. Its main applications include identifying the ...

Mass-Sensitive Particle Tracking to Characterize Membrane-Associated Macromolecule Dynamics

Short-lived or transient interactions of macromolecules at and with lipid membranes, an interface where a multitude of essential biological reactions take place, are inherently difficult to assess with standard biophysical methods. The introduction of mass-sensitive particle tracking (MSPT) constitutes an important step toward a thorough quantitative characterization of such processes. Technically, this was made possible through the advent of interferometric scattering microscopy (iSCAT)-based mass photometry (MP). When the background removal strategy is optimized to reveal the two-dimensional motion of membrane-associated particles, this technique allows the real-time analysis of both diffusion and molecular mass of unlabeled macromolecules on biological membranes. Here, a detailed protocol to perform and analyze mass-sensitive particle tracking of membrane-associated systems is described. Measurements performed on a commercial mass photometer achieve time resolution in the millisecond regime and, depending on the MP system, a mass detection limit down to 50 kDa. To showcase the potential of MSPT for the in-depth analysis of membrane-catalyzed macromolecule dynamics in general, results obtained for exemplary protein systems such as the native membrane interactor annexin V are presented.

This protocol describes an iSCAT-based image processing and single-particle tracking approach that enables the simultaneous investigation of the molecular mass and the diffusive behavior of macromolecules interacting with lipid membranes. Step-by-step instructions for sample preparation, mass-to-contrast conversion, movie acquisition, and post-processing are provided alongside directions to prevent potential pitfalls.

Short-lived or transient interactions of macromolecules at and with lipid membranes, an interface where a multitude of essential biological reactions take ...

OLIgo Mass Profiling (OLIMP) of Extracellular Polysaccharides

The direct contact of cells to the environment is mediated in many organisms by an extracellular matrix. One common aspect of extracellular matrices is that they contain complex sugar moieties in form of glycoproteins, proteoglycans, and/or polysaccharides. Examples include the extracellular matrix of humans and animal cells consisting mainly of fibrillar proteins and proteoglycans or the polysaccharide based cell walls of plants and fungi, and the proteoglycan/glycolipid based cell walls of bacteria. All these glycostructures play vital roles in cell-to-cell and cell-to-environment communication and signalling.
An extraordinary complex example of an extracellular matrix is present in the walls of higher plant cells. Their wall is made almost entirely of sugars, up to 75% dry weight, and consists of the most abundant biopolymers present on this planet. Therefore, research is conducted how to utilize these materials best as a carbon-neutral renewable resource to replace petrochemicals derived from fossil fuel. The main challenge for fuel conversion remains the recalcitrance of walls to enzymatic or chemical degradation due to the unique glycostructures present in this unique biocomposite.
Here, we present a method for the rapid and sensitive analysis of plant cell wall glycostructures. This method OLIgo Mass Profiling (OLIMP) is based the enzymatic release of oligosaccharides from wall materials facilitating specific glycosylhydrolases and subsequent analysis of the solubilized oligosaccharide mixtures using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF/MS)1 (Figure 1). OLIMP requires walls of only 5000 cells for a complete analysis, can be performed on the tissue itself2, and is amenable to high-throughput analyses3. While the absolute amount of the solubilized oligosaccharides cannot be determined by OLIMP the relative abundance of the various oligosaccharide ions can be delineated from the mass spectra giving insights about the substitution-pattern of the native polysaccharide present in the wall.
OLIMP can be used to analyze a wide variety of wall polymers, limited only by the availability of specific enzymes4. For example, for the analysis of polymers present in the plant cell wall enzymes are available to analyse the hemicelluloses xyloglucan using a xyloglucanase5, 11, 12, 13, xylan using an endo-&beta;-(1-4)-xylanase 6,7, or for pectic polysaccharides using a combination of a polygalacturonase and a methylesterase 8. Furthermore, using the same principles of OLIMP glycosylhydrolase and even glycosyltransferase activities can be monitored and determined 9.

OLIgo Mass Profiling OLIMP of Extracellular Polysaccharides

A rapid way is described to gain insights into the structure of polysaccharides in an extracellular matrix. The method takes advantage of the specificity of glycosylhydrolases and the sensitivity of mass spectrometry allowing minute amounts of materials to be analyzed. This technique is adaptable to be used directly on tissue itself.

The direct contact of cells to the environment is mediated in many organisms by an extracellular matrix. One common aspect of extracellular matrices is ...

Biology

Quantification of Proteins Using Peptide Immunoaffinity Enrichment Coupled with Mass Spectrometry

There is a great need for quantitative assays in measuring proteins. Traditional sandwich immunoassays, largely considered the gold standard in quantitation, are associated with a high cost, long lead time, and are fraught with drawbacks (e.g. heterophilic antibodies, autoantibody interference, 'hook-effect').1 An alternative technique is affinity enrichment of peptides coupled with quantitative mass spectrometry, commonly referred to as SISCAPA (Stable Isotope Standards and Capture by Anti-Peptide Antibodies).2 In this technique, affinity enrichment of peptides with stable isotope dilution and detection by selected/multiple reaction monitoring mass spectrometry (SRM/MRM-MS) provides quantitative measurement of peptides as surrogates for their respective proteins. SRM/MRM-MS is well established for accurate quantitation of small molecules 3, 4 and more recently has been adapted to measure the concentrations of proteins in plasma and cell lysates.5-7 To achieve quantitation of proteins, these larger molecules are digested to component peptides using an enzyme such as trypsin. One or more selected peptides whose sequence is unique to the target protein in that species (i.e. "proteotypic" peptides) are then enriched from the sample using anti-peptide antibodies and measured as quantitative stoichiometric surrogates for protein concentration in the sample. Hence, coupled to stable isotope dilution (SID) methods (i.e. a spiked-in stable isotope labeled peptide standard), SRM/MRM can be used to measure concentrations of proteotypic peptides as surrogates for quantification of proteins in complex biological matrices. The assays have several advantages compared to traditional immunoassays. The reagents are relatively less expensive to generate, the specificity for the analyte is excellent, the assays can be highly multiplexed, enrichment can be performed from neat plasma (no depletion required), and the technique is amenable to a wide array of proteins or modifications of interest.8-13 In this video we demonstrate the basic protocol as adapted to a magnetic bead platform.

Stable Isotope Standards and Capture by Anti-Peptide Antibodies (SISCAPA) couples affinity enrichment of peptides with stable isotope dilution mass spectrometry (MRM-MS) to provide quantitative measurement of peptides as surrogates for their respective proteins. Here we describe the protocol using magnetic particles in a partially automated format.