Team:ESBS-Strasbourg/Labeling

From 2008.igem.org

Fluorescence labeling

If one wants to work with multiple fluorescent proteins one has a great variety of XFPs to chose from. This choice is even more difficult if more than one XFP is needed.
The main issue is the overlapping of the different extinction/emission curves. Therefore one has to pay attention to the particular maxima. For example for our system already for the first bit it is crucial to work with suitable fluorescent markers.

Thus the purpose of this site is to give an overview for working with multiple fluorescence markers and to ease the decision which to take.

Multiple labeling

Recommended filter sets (Shaner C. et al)
Propose cyan,yellow,orange and red => minimal crosstalk
Said to be suitable for multiple labeling but forming tetramers (toxicity)




Features

DNA binding domains
Name Excitation (nm) Emission (nm) taken from reference sequence available work experimentally remarks
GFPmut3b 501 511 biobrick registry BBa E0040 yes yes
EYFP 515 528 biobrick registry BBa Jb3001 yes yes
ECFP 439 476 biobrick registry BBa E0022 yes  ? sequence without IRES
Highly RFP 584 607 biobrick registry BBa E1010 yes  ?
BFP 456/467/448 PDB yes  ?
OFP PDB AY678265 yes  ?
BFP 382 440 Lab yes  ? plasmid
RFP 561 583 Lab yes  ? plasmid


  • List from Clontech => Overview of available fluorescent proteins and their specifications

Biobricks

FPs that are available from the registry in standardized Biobrick-form

Yeast specific:

  • BBa_J63001, BBa_E2030 -enhanced version of EYFP, yeast-optimized YFP
  • BBa_E2020 -enhanced version of ECFP, yeast-optimized (works?)
  • BBa_E2050 -derivative of mRFP1, yeast-optimized (works?) => mOrange
  • BBa_E2060 -derivative of mRFP1, yeast-optimized (works?) => mCherry


Notes:

  • Contains N- and C-terminal linker sequences (with homology to biobrick parts BBa_E2060 (mCherry), BBa_E2050 (mOrange), and BBa_E2020 (Cerulean CFP) to facilitate color swapping in yeast.
  • Adds N-"MATSG" and "GSGTA"-C. to published amino acid sequence.
  • Inserts a "V" after normal start M.
  • Double TAATAA stop codon.
  • Missing EcoRI, HindIII, NotI, NdeI, XhoI, RsrII, BamHI, NcoI, BglI, SpeI, XbaI, and PstI.
  • Except for 5' and 3' ends no significant sequence identity runs with Cerulean CFP (BBa_E2020) or to GFP S65T as found in O'Shea deletion strain collection (originally from plasmid pFA6-GFP(S65T)-His3MX6).