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5 protocols using sep pak c18 spe column

1

Quantitative Proteomic Analysis of Post-Translational Modifications

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Media and heavy lysine ([2H4]-L-lysine and [13C6, 15N2]-L-lysine) were purchased from Cambridge Isotope Laboratories (Andover, MA). The reagents of trichloroacetic acid (TCA), dithiothreitol (DTT), iodoacetamide (IAA), trifluoroacetic acid (TFA), ammonium bicarbonate (NH4HCO3) and ammonium formate were all purchased from Sigma-Aldrich (St. Louis, MO, USA). Acetonitrile (ACN) and pure water were obtained from Thermofisher (Waltham, MA, USA). 2-D Quant kit was obtained from GE Healthcare (Buckinghamshire, United Kingdom). Trypsin was from Promega (Fitchburg, WI, USA). Protease inhibitor cocktail set III was obtained from Millipore (Billerica, MA, USA). Anti-acetyllysine antibody agarose beads were purchased from PTM Biolabs (Cat. No. 104, PTM Biolabs, Hangzhou, China). Sep-Pak C18 SPE columns were purchased from Waters (Framingham, USA).
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2

Quantitative Proteome-wide Succinylation Analysis

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The reagents, namely trichloroacetic acid (TCA), dithiothreitol (DTT), iodoacetamide (IAA), trifluoroacetic acid (TFA), ammonium bicarbonate (NH4HCO3) and ammonium formate, were all purchased from Sigma-Aldrich (St. Louis, MO, USA). Acetonitrile (ACN) and pure water were obtained from Thermofisher (Waltham, MA, USA), while 2-D Quant kit was obtained from GE Healthcare (Buckinghamshire, United Kingdom). Trypsin was purchased from Promega (Fitchburg, WI, USA) and the protease inhibitor cocktail set IV was obtained from Millipore (Billerica, MA, USA). The anti-succinyllysine antibody agarose conjugated beads were obtained from PTM Biolabs (Hangzhou, China) and Sep-Pak C18 SPE columns were purchased from Waters (Framingham, USA).
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3

Alzheimer's Disease Brain Proteome Analysis

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Human tissues of prefrontal cortical
regions were provided by the
Brain and Body Donation Program at Banner Sun Health Research Institute.
The AD case with short post-mortem interval (<3 h) was clinically
and pathologically characterized in accordance with established criteria.32 (link) This study was approved by Banner Sun Health
Research Institute. Adult rat brains were purchased from Pel Freez
Biologicals, and rat brain peptides were prepared as previously described.33 (link) The cerebral cortex of AD brain was homogenized
in 100 μL of lysis buffer (0.1 M Tris, pH 8.5, 8 M urea, 0.15%
sodium deoxycholate) at 4 °C using 0.5 mm glass beads for 5 min
in a Bullet Blender instrument (Next Advance).34 (link),35 (link) The entire cell lysate without clarification of the insoluble materials
was digested with Lys-C (Wako, 200:1 by weight) at room temperature
for 0.5 h in the lysis buffer, followed by trypsin digestion (Promega,
200:1 by weight) in 2 M urea, 0.1 M Tris-HCl, pH 8.5 at room temperature
overnight. The peptides were then acidified with 0.15% TFA, precleared
by centrifugation, desalted with Sep-Pak C18 SPE column (Waters),
and eluted with 40% acetonitrile (ACN) plus 0.1%TFA. The eluent was
dried and stored at −80 °C for further usage.15 (link) Protein quantification was carried out by short
SDS-gel-based staining and BCA method.31 (link)
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4

Protein Quantification and Digestion

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The protein concentration of the supernatants was estimated by the bicinchoninic acid protein assay. One hundred microgram of protein of each sample was adjusted to a final volume of 100 μL with 100 mM triethylammonium bicarbonate (TEAB), followed by adding 5 μL of 200 mM DTT and incubating at 55°C for 1 h. Afterwards, 5 μL of iodoacetamide (375 mM) was added to each sample, followed by 30 min incubation in dark at room temperature. Then the protein was precipitated with ice-cold acetone and redissolved in TEAB (20 μL). Proteins were digested with sequence-grade modified trypsin (Promega, Madison, WI) and labeled using the iTRAQ reagents kit. The labeled samples were combined, desalted (Sep-Pak C18 SPE column, Waters, Milford, MA), and vacuum dried.
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5

Chiral Analysis of Amino Acids

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The chirality of each amino acid of 14 was analyzed by HPLC as described previously in the literature [6 (link)]. Compounds 14 (each 1.5 mg) were subjected to hydrolysis with 6N HCl (0.5 mL) in a sealed tube at 110 °C for 20 h. Upon cooling, the acid in the hydrolysate was removed by Sep-Pak C18 SPE column (0.5 g, Waters), and the analyte eluted by aqueous methanol was subjected to chiral analysis on a Chirex 3126 (d)-penicillamine column, 4.6 i.d. × 250 mm, with an eluent system containing 2 mM CuSO4aq at a flow rate of 1 mL/min in an either isocratic or gradient mode. The detector was set at UV 254 nm. All the analytical conditions and data of the hydrolysates and authentic standards were supplemented in Tables S1–S4.
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