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Polarization-resolved second-harmonic generation microscopy as a method to visualize protein-crystal domains.


ABSTRACT: Polarization-resolved second-harmonic generation (PR-SHG) microscopy is described and applied to identify the presence of multiple crystallographic domains within protein-crystal conglomerates, which was confirmed by synchrotron X-ray diffraction. Principal component analysis (PCA) of PR-SHG images resulted in principal component 2 (PC2) images with areas of contrasting negative and positive values for conglomerated crystals and PC2 images exhibiting uniformly positive or uniformly negative values for single crystals. Qualitative assessment of PC2 images allowed the identification of domains of different internal ordering within protein-crystal samples as well as differentiation between multi-domain conglomerated crystals and single crystals. PR-SHG assessments of crystalline domains were in good agreement with spatially resolved synchrotron X-ray diffraction measurements. These results have implications for improving the productive throughput of protein structure determination through early identification of multi-domain crystals.

SUBMITTER: DeWalt EL 

PROVIDER: S-EPMC3532131 | biostudies-literature | 2013 Jan

REPOSITORIES: biostudies-literature

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Polarization-resolved second-harmonic generation microscopy as a method to visualize protein-crystal domains.

DeWalt Emma L EL   Begue Victoria J VJ   Ronau Judith A JA   Sullivan Shane Z SZ   Das Chittaranjan C   Simpson Garth J GJ  

Acta crystallographica. Section D, Biological crystallography 20121220 Pt 1


Polarization-resolved second-harmonic generation (PR-SHG) microscopy is described and applied to identify the presence of multiple crystallographic domains within protein-crystal conglomerates, which was confirmed by synchrotron X-ray diffraction. Principal component analysis (PCA) of PR-SHG images resulted in principal component 2 (PC2) images with areas of contrasting negative and positive values for conglomerated crystals and PC2 images exhibiting uniformly positive or uniformly negative valu  ...[more]

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