Materials and Reagents

Purified protein with chitin binding affinity
Note: We used histidine-tagged chitin binding protein CbpD. The protein was purified by affinity chromatography onto a 5-ml HisTrap nickel column (Pharmacia) on an Äkta system (Amersham Biosciences). The complete purification protocol is described in details in Cadoret et al. (2014).
Chitin beads (New England Biolabs, catalog number: S6651 )
Tris Base
EDTA
NaCl
Tween 100
Freshly made solution of chitin binding buffer (see Recipes)

Equipment

Laboratory vortex adapted to Eppendorf tubes
Laboratory rotating wheel adapted to Eppendorf tubes
Cold room or refrigerated incubator (4 °C)

Procedure

Wash the chitin beads as follows
1. Vortex the chitin beads before pipetting.
2. Wash the desired amount of beads solution (100 µl per experiment) twice with 5 volumes of chitin binding buffer. This washing step is performed by gravity flow by leaving the sample 5 min at room temperature.
Binding assay
1. Prepare a 200 µl solution of chitin-binding buffer containing the purified CbpD protein at 60 µg/ml (total fraction). For that, 1.5 µl of purified CbpD at 8 mg/ml in 50 mM Tris pH 8, 300 mM NaCl, 250 mM imidazole was mixed with 198. 5 µl of chitin binding buffer.
2. Add 100 µl of pre-washed chitin beads in chitin-binding buffer to the purified protein solution.
3. Incubate the sample on a laboratory rotating wheel for 90 min at 4 °C.
4. After gravity flow separation, collect the supernatant (unbound fraction).
5. Wash the beads (bound fraction) twice with 200 µl of chitin binding buffer by gravity flow.
6. Analyse 15 μl of Total (equivalent to 0.9 μg), Unbound and Bound fractions by SDS-PAGE followed by Coomassie blue staining and/or immunoblotting (see Figure 1).

Representative data

Figure 1. Chitin-binding affinity of CbpD. To test the chitin-binding affinity of CbpD, a solution of purified CbpD at 200 μg/ml in chitin binding buffer (Total) was incubated with chitin beads according to the present protocol. 15 μl samples of Total, Unbound and Bound fractions were analyzed by SDS-PAGE followed by Coomassie blue staining. Molecular mass markers (in kDa) are indicated on the left.

Notes

The chitin binding buffer and the protein solution in chitin binding buffer must be freshly prepared.
A negative control can consist of the same experiment where the chitin beads solution is replaced by chitin binding buffer.
Additionally, purified proteins without chitin binding affinity such as Elastase (LasB) and exotoxin A (ToxA) can be used as negative control [see Figure 5B in Cadoret et al. (2014)].

Recipes

Freshly made solution of chitin binding buffer
Chitin binding buffer:
50 mM Tris HCl (pH 8)
1 mM EDTA (pH 8)
500 mM NaCl
0.1% Tween 100
The chitin binding buffer is prepared from stock solutions:
Tris HCl 1 M (pH 8)
EDTA 0.5 M (pH 8)
NaCl 5 M

Acknowledgments

This protocol adapted from Shutinoski et al. (2010) was used in Cadoret et al. (2014). The work is funded by a Ph.D. grant from the French government.

References

Cadoret, F., Ball, G., Douzi, B. and Voulhoux, R. (2014). Txc, a new type II secretion system of Pseudomonas aeruginosa strain PA7, is regulated by the TtsS/TtsR two-component system and directs specific secretion of the CbpE chitin-binding protein. J Bacteriol 196(13): 2376-2386.
Shutinoski, B., Schmidt, M. A. and Heusipp, G. (2010). Transcriptional regulation of the Yts1 type II secretion system of Yersinia enterocolitica and identification of secretion substrates. Mol Microbiol 75(3): 676-691.