2a56: Difference between revisions
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'''fluorescent protein asFP595, A143S, on-state, 5min irradiation''' | '''fluorescent protein asFP595, A143S, on-state, 5min irradiation''' | ||
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[[Category: Wahl, M C.]] | [[Category: Wahl, M C.]] | ||
[[Category: Weber, G.]] | [[Category: Weber, G.]] | ||
[[Category: | [[Category: Ascp]] | ||
[[Category: | [[Category: Chromoprotein]] | ||
[[Category: | [[Category: Fluorescent protein]] | ||
[[Category: | [[Category: Photochromic protein]] | ||
[[Category: | [[Category: Reversible photoswitch]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 18:37:09 2008'' | |||
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Revision as of 18:37, 3 May 2008
fluorescent protein asFP595, A143S, on-state, 5min irradiation
OverviewOverview
Proteins that can be reversibly photoswitched between a fluorescent and a nonfluorescent state bear enormous potential in diverse fields, such as data storage, in vivo protein tracking, and subdiffraction resolution light microscopy. However, these proteins could hitherto not live up to their full potential because the molecular switching mechanism is not resolved. Here, we clarify the molecular photoswitching mechanism of asFP595, a green fluorescent protein (GFP)-like protein that can be transferred from a nonfluorescent "off" to a fluorescent "on" state and back again, by green and blue light, respectively. To this end, we establish reversible photoswitching of fluorescence in whole protein crystals and show that the switching kinetics in the crystal is identical with that in solution. Subsequent x-ray analysis demonstrated that upon the absorption of a green photon, the chromophore isomerizes from a trans (off) to a cis (on) state. Molecular dynamics calculations suggest that isomerization occurs through a bottom hula twist mechanism with concomitant rotation of both bonds of the chromophoric methine ring bridge. This insight into the switching mechanism should facilitate the targeted design of photoswitchable proteins. Reversible photoswitching of the protein chromophore system within intact crystals also constitutes a step toward the use of fluorescent proteins in three-dimensional data recording.
About this StructureAbout this Structure
2A56 is a Protein complex structure of sequences from Anemonia sulcata. Full crystallographic information is available from OCA.
ReferenceReference
Structure and mechanism of the reversible photoswitch of a fluorescent protein., Andresen M, Wahl MC, Stiel AC, Grater F, Schafer LV, Trowitzsch S, Weber G, Eggeling C, Grubmuller H, Hell SW, Jakobs S, Proc Natl Acad Sci U S A. 2005 Sep 13;102(37):13070-4. Epub 2005 Aug 31. PMID:16135569 Page seeded by OCA on Sat May 3 18:37:09 2008