Our reporting standards for fluorescent proteins – Feedback wanted

Several years ago, based on informal input from various members of the community, Nature Methods established some internal minimum reporting standards for manuscripts describing new or improved fluorescent proteins. These were never formally reported but were often communicated to authors of submitted manuscripts when the characterization data provided didn’t meet these standards.

Recently we were fortunate enough to be able to meet with a substantial number of fluorescent protein developers to informally endorse and revise these standards. Our revised reporting requirements for fluorescent proteins are listed below.

Minimum reporting requirements for fluorescent proteins

  1. Full absorption and excitation (250nm to 750nm) and emission curves (350nm to 950nm) under single-photon excitation and at least some data under 2-photon excitation
  2. Values for quantum yield, extinction coefficient, brightness and pKa
  3. Gel filtration data to show that the protein is monomeric or acknowledgement that it isn’t monomeric
  4. Data on fluorophore maturation time including the final maturation percentage. Detailed protocol must be provided
  5. Image data on several representative protein fusions to show that it does not disrupt protein function. This should include tubulin since it is pretty universally used for this purpose
  6. In vitro photostability data compared to other representative proteins. At a minimum this should be decay curves under widefield and confocal illumination to test two different irradiation intensity regimes. Ideally, graphs of the decay time constant versus power should be provided
  7. Cytotoxicity measured in mammalian cells by flow cytometry and compared to EGFP and at least one established fluorescent protein in the spectral range of the reported protein

We also used this opportunity to set some standards for photoswitchable fluorescent proteins. These proteins display quite complicated behaviors and the desired characteristics can vary depending on the application. An example of this is the different characteristics desired for (f)PALM/STORM vs RESOLFT or SSIM super-resolution imaging. These new reporting standards are listed below and supplement the ones above which would also apply to photoswitchable fluorescent proteins.

Additional minimum reporting requirements for photoswitchable FPs

  1. Graphs of 20+ cycles at different powers to observe decay with full details on power and methods
  2. Absorption spectra before and after photoconversion
  3. Optimal parameters for the best power and also for another power
  4. Measurement of how complete the switching is

We encourage developers and users of fluorescent proteins to comment on these minimal reporting standards. But more than that… we’d like your help in moving forward from here.

Are additional standards needed due to new developments?

Do we need standards similar to these in other areas?

We have found that enforcing common standards on highly related tools can greatly improve the efficiency and objectivity of the peer review process and help avoid holding similar developments to different standards. Of course, this requires flexibility in enforcement and we will always allow editor’s some discretion in enforcing these requirements when there is a legitimate reason for doing so.

Fluorescent Proteins and Sensors Webinar – Questions & Answers

Our very first webinar is now live. The topic is “Fluorescent protein and sensors: A practical discussion” and you can register to view it at www.nature.com/webcasts/fluorescent_proteins. Update: Registration link inactivated. Please go here to listen to the archived discussion in .mp3 format.

Nature Methods was joined by Robert Campbell, David Piston and Thomas Knopfel who have been developing and using fluorescent proteins and sensors for years. We had a nice discussion that provided good practical information for users of these tools. If you haven’t watched it, I encourage you to do so. If you watch the webcast within the first month it is live you have the opportunity to submit questions for our participants. Please use the form on the webcast viewing page to submit questions. There will be a delay in providing answers here on our blog while we consult with the participants.

Participants in fluorescent proteins and sensors webinar

Our participants: Robert Campbell, David Piston and Thomas Knopfel

Here we will be posting the questions we receive and answers from our participants. Readers may also comment directly on the blog below but we can not guarantee that any questions asked there will be answered. We do encourage anyone in the community to chime in with their response to any questions that are posed, even if they don’t agree with our participants.