Method Article

Isolation of Small Regulatory RNA–Bound Bacterial Target RNA Using Affinity Purification

August 29th, 2025

In This Article

Abstract

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Source: Mercier, N., et. al., MS2-Affinity Purification Coupled with RNA Sequencing in Gram-Positive Bacteria. J. Vis. Exp. (2021)

This video demonstrates the isolation of MS2-tagged small regulatory RNA (sRNA) bound to its bacterial target RNA using affinity purification with a maltose-binding protein (MBP)–MS2 coat protein fusion immobilized on amylose resin.

Protocol

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Buffers and media

For MAPS experiments, prepare the following buffers and media:- Buffer A (150 mM KCl, 20 mM Tris-HCl pH 8, 1 mM MgCl2 and 1 mM DTT)- Buffer E (250 mM KCl, 20 mM Tris-HCl pH 8, 12 mM maltose, 0.1% Triton, 1 mM MgCl2 and 1 mM DTT)

Column preparation

CAUTION: Be careful not to allow the amylose resin to dry. If needed, seal the column with an end-cap. Prepare all the solutions before starting the affinity purification.

  1. Put a chromatography column in a column rack.
  2. Remove the column tip and wash the column with ultrapure water.
  3. Add 300 µL of amylose resin.
  4. Wash the column with 10 mL of Buffer A.
  5. Dilute 1,200 pmol of MBP (Maltose-binding protein)-MS2 protein in 6 mL of Buffer A and load it into the column.
  6. Wash the column with 10 mL of Buffer A.

MS2-affinity purification (Figure 1)

  1. Load the cell lysate into the column.
    NOTE: Keep 1 mL of the cell lysate (Crude extract, CE) to extract total RNA and perform Northern blot and transcriptomic analysis.
  2. Collect the flow-through fraction (FT) in a clean collection tube.
  3. Wash the column 3 times with 10 mL of Buffer A. Collect the wash fraction (W).
  4. Elute the column with 1 mL of Buffer E and collect the elution fraction (E) in a 2 mL microtube.
  5. Keep all collected fractions on ice until RNA extraction or freeze them at -20 °C for later use.

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Results

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Plasmid construction, bacterial transformations, RNA extraction; diagram with Northern Blot results.

Figure 1. Schematic illustration of the MAPS protocol adapted to Staphylococcus aureu...

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
1.5 mL microcentrifuge tubeSarstedt72.690.001
15 mL centrifuge tubesFalcon352070
2 mL microcentrifuge tubeStarstedt72.691
250 mL culture flaskDominique Dutscher2515074Bacterial cultures
50 mL centrifuge tubesFalcon352051Culture centrifugation
Amylose resinNew England BioLabsE8021SMS2-affinity purification
pMBP-MS2Addgene65104MS2-MBP production
Poly-Prep chromatography columnBioRad7311550MS2-affinity purification

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Tags

MS2 Affinity PurificationRNA SequencingMaltose Binding ProteinAmylose ResinMS2 Coat ProteinCell LysateFlow Through FractionElution Buffer

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