2a56: Difference between revisions
New page: left|200px<br /><applet load="2a56" size="450" color="white" frame="true" align="right" spinBox="true" caption="2a56, resolution 1.90Å" /> '''fluorescent protein ... |
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[[Image:2a56.gif|left|200px]]<br /><applet load="2a56" size=" | [[Image:2a56.gif|left|200px]]<br /><applet load="2a56" size="350" color="white" frame="true" align="right" spinBox="true" | ||
caption="2a56, resolution 1.90Å" /> | caption="2a56, resolution 1.90Å" /> | ||
'''fluorescent protein asFP595, A143S, on-state, 5min irradiation'''<br /> | '''fluorescent protein asFP595, A143S, on-state, 5min irradiation'''<br /> | ||
==Overview== | ==Overview== | ||
Proteins that can be reversibly photoswitched between a fluorescent and a | 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 Structure== | ==About this Structure== | ||
2A56 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Anemonia_sulcata Anemonia sulcata]. Full crystallographic information is available from [http:// | 2A56 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Anemonia_sulcata Anemonia sulcata]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2A56 OCA]. | ||
==Reference== | ==Reference== | ||
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[[Category: Graeter, F.]] | [[Category: Graeter, F.]] | ||
[[Category: Grubmueller, H.]] | [[Category: Grubmueller, H.]] | ||
[[Category: Hell, S | [[Category: Hell, S W.]] | ||
[[Category: Jakobs, S.]] | [[Category: Jakobs, S.]] | ||
[[Category: Schaefer, L.]] | [[Category: Schaefer, L.]] | ||
[[Category: Stiel, A | [[Category: Stiel, A C.]] | ||
[[Category: Trowitzsch, S.]] | [[Category: Trowitzsch, S.]] | ||
[[Category: Wahl, M | [[Category: Wahl, M C.]] | ||
[[Category: Weber, G.]] | [[Category: Weber, G.]] | ||
[[Category: ascp]] | [[Category: ascp]] | ||
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[[Category: reversible photoswitch]] | [[Category: reversible photoswitch]] | ||
''Page seeded by [http:// | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:23:56 2008'' | ||
Revision as of 17:23, 21 February 2008
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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
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