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Selective detection of protein crystals by second harmonic microscopy.


ABSTRACT: The unique symmetry properties of second harmonic generation (SHG) microscopy enabled sensitive and selective imaging of protein microcrystals with negligible contributions from solvated proteins or amorphous protein aggregates. In studies of microcrystallites of green fluorescent protein (GFP) prepared in 500 pL droplets, the SHG intensities rivaled those of fluorescence, but with superb selectivity for crystalline regions. GFP in amorphous aggregates and in solution produced substantial background fluorescence, but no detectable SHG. The ratio of the forward-to-backward detected SHG provides a measure of the particle size, suggesting detection limits down to crystallites 100 nm in diameter under low magnification (10x). In addition to being sensitive and highly selective, second-order nonlinear optical imaging of chiral crystals (SONICC) is directly compatibility with virtually all common protein crystallization platforms.

SUBMITTER: Wampler RD 

PROVIDER: S-EPMC6905431 | biostudies-literature | 2008 Oct

REPOSITORIES: biostudies-literature

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Selective detection of protein crystals by second harmonic microscopy.

Wampler Ronald D RD   Kissick David J DJ   Dehen Christopher J CJ   Gualtieri Ellen J EJ   Grey Jessica L JL   Wang Hai-Feng HF   Thompson David H DH   Cheng Ji-Xin JX   Simpson Garth J GJ  

Journal of the American Chemical Society 20081003 43


The unique symmetry properties of second harmonic generation (SHG) microscopy enabled sensitive and selective imaging of protein microcrystals with negligible contributions from solvated proteins or amorphous protein aggregates. In studies of microcrystallites of green fluorescent protein (GFP) prepared in 500 pL droplets, the SHG intensities rivaled those of fluorescence, but with superb selectivity for crystalline regions. GFP in amorphous aggregates and in solution produced substantial backgr  ...[more]

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