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. Author manuscript; available in PMC: 2016 Feb 16.
Published in final edited form as: J Am Chem Soc. 2015 Aug 25;137(35):11303–11311. doi: 10.1021/jacs.5b04366

Figure 9.

Figure 9

The RAm1-P1 fluorescent conjugate is a cellular client-based thermo-labile sensor of proteostasis network capacity in E. coli. (a) P1 selectively binds to and reacts with RA in E. coli affording the RAm1-P1 conjugate. Thus, only cells transformed with RA exhibit conjugate fluorescence in the confocal image. (b) The pre-formed RAm1-P1 conjugate formed granular aggregate structures as observed by confocal fluorescence imaging (white arrows) after heating at 45 °C for 10 min, serving as a sensor of proteostasis network capacity insufficiency. (c) Transcriptional reprogramming of E. coli by over-expressing the σ32-I54N heat shock response transcription factor enhances the proteostasis network capacity of the cytosol protecting the preformed RAm1-P1 conjugate from aggregating upon application of thermal stress, as reflected by the lack of granular structures in rightmost confocal image in comparison to the image on the left where aggregation is observed because cytosolic proteostasis network capacity was not preemptively enhanced. Sample preparation and imaging details are described in experimental section of the supporting information. NT: Non-transformed. Images were taken using a Zeiss LSM710 confocal microscope.