Quantitative determination of fluorescence labeling implemented in cell cultures

Abstract

Abstract Background Labeling efficiency is a crucial parameter in fluorescence applications, especially when studying biomolecular interactions. Current approaches for estimating the yield of fluorescent labeling have critical drawbacks that usually lead them to be inaccurate or not quantitative. Results We present a method to quantify fluorescent-labeling efficiency that addresses the critical issues marring existing approaches. The method operates in the same conditions of the target experiments by exploiting a ratiometric evaluation with two fluorophores used in sequential reactions. We show the ability of the protocol to extract reliable quantification for different fluorescent probes, reagents concentrations, and reaction timing and to optimize labeling performance. As paradigm, we consider the labeling of the membrane-receptor TrkA through 4′-phosphopantetheinyl transferase Sfp in living cells, visualizing the results by TIRF microscopy. This investigation allows us to find conditions for demanding single and multi-color single-molecule studies requiring high degrees of labeling. Conclusions The developed method allows the quantitative determination and the optimization of staining efficiency in any labeling strategy based on stable reactions.

Keywords

• Fluorescent labeling
• Fluorescence microscopy
• Single-molecule imaging
• Single-particle tracking
• Membrane receptors
• Sfp phosphopantetheinyl transferase