Application of hybrid LRR technique to protein crystallization

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LRR family proteins play important roles in a variety of physiological processes. To facilitate their production and crystallization, we have invented a novel method termed "Hybrid LRR Technique". Using this technique, the first crystal structures of three TLR family proteins could be determined. In this review, design principles and application of the technique to protein crystallization will be summarized. For crystallization of TLRs, hagfish VLR receptors were chosen as the fusion partners and the TLR and the VLR fragments were fused at the conserved LxxLxLxxN motif to minimize local structural incompatibility. TLR-VLR hybridization did not disturb structures and functions of the target TLR proteins. The Hybrid LRR Technique is a general technique that can be applied to structural studies of other LRR proteins. It may also have broader application in biochemical and medical application of LRR proteins by modifying them without compromising their structural integrity.
Publisher
KOREAN SOCIETY BIOCHEMISTRY & MOLECULAR BIOLOGY
Issue Date
2008-05
Language
English
Article Type
Review
Keywords

LEUCINE-RICH REPEAT; TOLL-LIKE RECEPTORS; VARIABLE LYMPHOCYTE RECEPTORS; CRYSTAL-STRUCTURE; RIBONUCLEASE INHIBITOR; STRUCTURAL DIVERSITY; ADAPTIVE IMMUNITY; RECOGNITION; LIPOPOLYSACCHARIDE; COMPLEX

Citation

BMB REPORTS, v.41, no.5, pp.353 - 357

ISSN
1976-6696
URI
http://hdl.handle.net/10203/11073
Appears in Collection
CH-Journal Papers(저널논문)
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