4q7t

Crystal structure of photoswitchable fluorescent protein PSmOrange

spinqualitylabelsall models 4q7t, resolution 1.94Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 4q7t is a 2 chain structure. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. NonStd Res: OFM Related: 2h5o, 4q7r, 4q7u Resources: FirstGlance, OCA, RCSB, PDBsum Publication Abstract from PubMed A structural analysis of the recently developed orange fluorescent proteins with novel phenotypes, LSSmOrange (lambdaex/lambdaem at 437/572 nm), PSmOrange (lambdaex/lambdaem at 548/565 nm and for photoconverted form at 636/662 nm) and PSmOrange2 (lambdaex/lambdaem at 546/561 nm and for photoconverted form at 619/651 nm), is presented. The obtained crystallographic structures provide an understanding of how the ensemble of a few key mutations enabled special properties of the orange FPs. While only a single Ile161Asp mutation, enabling excited state proton transfer, is critical for LSSmOrange, other substitutions provide refinement of its special properties and an exceptional 120 nm large Stokes shift. Similarly, a single Gln64Leu mutation was sufficient to cause structural changes resulting in photoswitchability of PSmOrange, and only one additional substitution (Phe65Ile), yielding PSmOrange2, was enough to greatly decrease the energy of photoconversion and increase its efficiency of photoswitching. Fluorescence of photoconverted PSmOrange and PSmOrange2 demonstrated an unexpected bathochromic shift relative to the fluorescence of classic red FPs, such as DsRed, eqFP578 and zFP574. The structural changes associated with this fluorescence shift are of considerable value for the design of advanced far-red FPs. For this reason the chromophore transformations accompanying photoconversion of the orange FPs are discussed. Orange Fluorescent Proteins: Structural Studies of LSSmOrange, PSmOrange and PSmOrange2.,Pletnev S, Shcherbakova DM, Subach OM, Pletneva NV, Malashkevich VN, Almo SC, Dauter Z, Verkhusha VV PLoS One. 2014 Jun 24;9(6):e99136. doi: 10.1371/journal.pone.0099136. eCollection, 2014. PMID:24960050 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

Proteopedia Page Contributors and Editors (what is this?)

OCA