Dataset Information

High-yield production of human Dicer by transfection of human HEK293-EBNA1 cells grown in suspension.

ABSTRACT:

Background

Dicer is a 219-kDa protein that plays key roles in gene regulation, particularly as the ribonuclease III enzyme responsible for cleaving precursor miRNA substrates. Its enzymatic activity is highly regulated by protein factors, and this regulation can impact on the levels of miRNAs and modulate the behavior of a cell. To better understand the underlying mechanisms of regulation, detailed enzymatic and structural characterization of Dicer are needed. However, these types of studies generally require several milligrams of recombinant protein, and efficient preparation of such quantities of pure human Dicer remains a challenge. To prepare large quantities of human Dicer, we have optimized transfection in HEK293-6E cells grown in suspension and streamlined a purification procedure.

Results

Transfection conditions were first optimized to achieve expression levels between 10 and 18?mg of recombinant Dicer per liter of culture. A three-step purification protocol was then developed that yields 4-9?mg of purified Dicer per liter of culture in a single day. From SEC-MALS/RI analysis and negative stain TEM, we confirmed that the purified protein is monomerically pure ( ? 98%) and folds with the characteristic L-shape geometry. Using an electrophoretic mobility shift assay, a dissociation constant (K_d) of 5?nM was measured for Dicer binding to pre-let-7a-1, in agreement with previous reports. However, when probing the cleavage activity of Dicer for pre-let-7a-1, we measured k_cat (7.2?±?0.5?min^-?1) and K_M (1.2?±?0.3??M) values that are much higher than previously reported due to experimental conditions that better respect the steady-state assumption.

Conclusions

The expression and purification protocols described here provide high yields of monomerically pure and active human Dicer. Cleavage studies of a pre-let-7 substrate with this purified Dicer reveal higher k_cat and K_M values than previously reported and support the current view that conformational changes are associated with substrate binding. Large quantities of highly pure Dicer will be valuable for future biochemical, biophysical and structural investigations of this key protein of the miRNA pathway.

SUBMITTER: Bouvette J

PROVIDER: S-EPMC6282390 | biostudies-literature | 2018 Dec

REPOSITORIES: biostudies-literature

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Publications

High-yield production of human Dicer by transfection of human HEK293-EBNA1 cells grown in suspension.

Bouvette Jonathan J Korkut Dursun Nizam DN Fouillen Aurélien A Amellah Soumiya S Nanci Antonio A Durocher Yves Y Omichinski James G JG Legault Pascale P

BMC biotechnology 20181206 1

<h4>Background</h4>Dicer is a 219-kDa protein that plays key roles in gene regulation, particularly as the ribonuclease III enzyme responsible for cleaving precursor miRNA substrates. Its enzymatic activity is highly regulated by protein factors, and this regulation can impact on the levels of miRNAs and modulate the behavior of a cell. To better understand the underlying mechanisms of regulation, detailed enzymatic and structural characterization of Dicer are needed. However, these types of stu ...[more]

PMID: 30522464

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Dataset Information

High-yield production of human Dicer by transfection of human HEK293-EBNA1 cells grown in suspension.

Background

Results

Conclusions

Publications

High-yield production of human Dicer by transfection of human HEK293-EBNA1 cells grown in suspension.

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