Crysalis: an integrated server for computational analysis and design of protein crystallization

• Published in: Scientific reports Vol. 6; no. 1; p. 21383
• Main Authors: Wang, Huilin, Feng, Liubin, Zhang, Ziding, Webb, Geoffrey I., Lin, Donghai, Song, Jiangning
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 24-02-2016; Nature Publishing Group
• Subjects: 42/70; 631/114/1305; 631/114/2410; 631/114/2784; 631/114/663/2009; 82/80; 82/83; Amino Acid Sequence; Bioinformatics; Computational Biology; Computer applications; Crystallization; Crystallography, X-Ray; Crystals; Databases, Protein; Design; Diffraction; Humanities and Social Sciences; Machine Learning; Molecular Sequence Annotation; multidisciplinary; Physicochemical properties; Protein structure; Proteins; Proteins - chemistry; Proteomes; Regression analysis; Science; Software
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/srep21383

The failure of multi-step experimental procedures to yield diffraction-quality crystals is a major bottleneck in protein structure determination. Accordingly, several bioinformatics methods have been successfully developed and employed to select crystallizable proteins. Unfortunately, the majority of existing
in silico
methods only allow the prediction of crystallization propensity, seldom enabling computational design of protein mutants that can be targeted for enhancing protein crystallizability. Here, we present Crysalis, an integrated crystallization analysis tool that builds on support-vector regression (SVR) models to facilitate computational protein crystallization prediction, analysis, and design. More specifically, the functionality of this new tool includes: (1) rapid selection of target crystallizable proteins at the proteome level, (2) identification of site non-optimality for protein crystallization and systematic analysis of all potential single-point mutations that might enhance protein crystallization propensity, and (3) annotation of target protein based on predicted structural properties. We applied the design mode of Crysalis to identify site non-optimality for protein crystallization on a proteome-scale, focusing on proteins currently classified as non-crystallizable. Our results revealed that site non-optimality is based on biases related to residues, predicted structures, physicochemical properties, and sequence loci, which provides in-depth understanding of the features influencing protein crystallization. Crysalis is freely available at
http://nmrcen.xmu.edu.cn/crysalis/
.