High-throughput Hisx6-tagged protein purification

doi:10.1038/nprot.2007.544

Method Article

High-throughput Hisx6-tagged protein purification

https://doi.org/10.1038/nprot.2007.544

This protocol has been posted on Protocol Exchange, an open repository of community-contributed protocols sponsored by Nature Portfolio. These protocols are posted directly on the Protocol Exchange by authors and are made freely available to the scientific community for use and comment.

Version 1

posted 19 Dec, 2007

You are reading this latest protocol version

high-throughput

protein purification

We have developed a high-throughput protein purification protocol that allows us to purify ~4,000 proteins within 10 hours from prepared culture. By combining steps of cell lysis and protein capture on affinity resins in sealed filter plates, we reduced the number of pipetting steps and thus, human errors.

Q-Fill2

Re-suspend cell pellets at 4 °C in 80 µL of lysis buffer, containing 50 mM NaH₂PO₄ at pH 8 with 300 mM NaCl, 20 mM imidazole, CelLytic B (Sigma), Lysozyme (1 mg/mL), Benzonase (50 units/mL), proteinase inhibitor cocktail (Sigma), and PMSF (1 mM/mL).
Wash Ni-NTA Superflow (QIAGEN) twice with water and twice with 50 mM NaH₂PO₄ at pH 8 with 300 mM NaCl, 20 mM imidazole using centrifugation.
Add 25 μL pre-washed Ni-NTA Superflow (QIAGEN) to each well
Transfer the mixtures into bottom-sealed filter plates (Multiscreen Nylon Mesh)
Seal the filter plates
Incubated for 1.5 hr at 4 °C with vigorously shaking
Remove seals
Wash the resin-protein complexes 3 times with 250 µL/well of wash buffer I (50 mM NaH₂PO₄ with 300 mM NaCl, 10% glycerol, 20 mM imidazole, 0.01% Triton X-100, at pH 8) and 3 times with Wash buffer II (50 mM NaH₂PO₄ with 150 mM NaCl, 25% glycerol, 20 mM imidazole, 0.01% Triton X-100, at pH 8) using a Q-fill2 (Gentix, UK).
Spin the filter plates
Add 25 μL of elution buffer (50 mM NaH₂PO₄/150 mM NaCl/25% glycerol/250 mM imidazole/0.01% Triton X-100, pH 7.5)
Incubate 15 min at 4 °C
Elute proteins into 96-well receiver plates by centrifugation.
Repeat 10-12
Store the proteins in 96-well plates at -80 °C

10 hours

This work is supported in part by the National Institute of Health (GM071440 to C.H.; U54 RR020839 to H.Z.), W. M. Keck Foundation (to C.H.), the Arnold and Mabel Beckman Foundation (to C.H.), and the Research Corporation (to C.H.).

PDF

Version 1

posted 19 Dec, 2007

You are reading this latest protocol version

High-throughput Hisx6-tagged protein purification

Status:

Version 1

Introduction

Equipment

Procedure

Timing

Acknowledgements

Associated Publications

Status:

Version 1

Privacy Policy

Terms of Service