FRET evidence that an isoform of caspase-7 binds but does not cleave its substrate.

A caspase-7 biosensor (vDEVDc) based on FRET (fluorescence resonance energy transfer) was used to study the proteolytic properties of caspase-7, an executioner protease in cellular apoptosis. An active isoform of caspase-7 with the 56 N-terminal residues truncated (57casp7) cleaved vDEVDc at the recognition sequence, resulting in a FRET efficiency decrease of 61%. In contrast, an isoform with the 23 N-terminal residues truncated (24casp7) bound to vDEVDc but did not cleave the substrate, resulting in a FRET increase of 15%. Kinetic results showed an exponential substrate cleavage and binding curve for the 57casp7 and 24casp7 isoforms, respectively. FRET changes of the vDEVDc biosensor were also monitored in cos-7 cells upon STS-induced apoptosis. Finally, we modeled caspase-7 binding to vDEVDc and estimated a FRET emission ratio increase of 31.7%, which agrees with the 15% experimental result. We showed that two differently truncated isoforms of caspase-7 exhibit different enzymatic properties, namely binding by 24casp7 and hydrolysis by 57casp7.

Computational modeling of a new fluorescent biosensor for caspase proteolytic activity improves dynamic range.

The class of fluorescence resonance energy transfer (FRET) protein biosensors that are useful for measuring protease activity is composed of a tandem fusion of yellow fluorescent protein (YFP), a cleavage recognition sequence, and cyan fluorescent protein (CFP). The dynamic range of these FRET-based protein biosensors is often weak, but applications such as high throughput drug screening require stronger dynamic ranges. Using the biosensor for the caspase-3 protease as an example, here we showed a computational approach to improve the FRET dynamic range based on the atomic structure of caspase-3 bound to its inhibitor. This result was verified from our experiments where the FRET dynamic range improved by at least 60% on average in both in vitro and in vivo contexts. In concept, the same strategy can be applied to improve dynamic range of other FRET-based protein biosensors for protease activity where there exist solved atomic structures for protein complexes.

FRET evidence that an isoform of caspase-7 binds but does not cleave its substrate.

Caspase-7 is one of the executioner proteases in cellular apoptosis. Its kinetics has been monitored using biosensors based on the principle of fluorescence resonance energy transfer (FRET). Here, a caspase-7 biosensor (named vDEVDc) using fluorescent proteins as the donor and acceptor of FRET was used to study the biochemical properties of caspase-7. An active isoform of caspase-7 with the 56 N-terminal residues truncated (named 57casp7) cleaved the vDEVDc biosensor at the recognition sequence, resulting in a FRET efficiency decrease of 61%. In contrast, another caspase-7 isoform with the 23 N-terminal residues truncated (named 24casp7) bound the vDEVDc biosensor without cleaving the substrate, resulting in a FRET increase of 15%. The kinetics of the two caspase-7 isoforms were studied by monitoring the FRET change of the vDEVDc biosensor over time, which showed an exponential substrate cleavage and binding curve for the 57casp7 and 24casp7 isoform, respectively. Lastly, we modeled caspase-7 binding to the vDEVDc biosensor and estimated a FRET emission ratio increase of 16.2% after binding to caspase-7, which agrees with the 15% experimental result. We showed that two isoforms of caspase-7 with differently truncated prodomain exhibit different enzymatic properties, namely binding by the 24casp7 isoform and hydrolysis by 57casp7. We also demonstrated that our FRET biosensor (vDEVDc) can be used to detect not only the substrate cleavage event, but also the substrate binding event.

Creation of circularly permutated yellow fluorescent proteins using fluorescence screening and a tandem fusion template.

By experimenting with many different circularly permutated yellow fluorescent protein (cpYFP) variants as acceptors in fluorescence resonance energy transfer based biosensors, the optimal dynamic range can be discovered by sampling the possibilities of relative fluorophore orientations before and after bioactivity. Hence, to facilitate the sampling process, we introduced a new approach to construct a library of cpYFP variants using fluorescence screening and a tandem fusion template. This new approach is rapid because it does not require creating intermediate N- and C-terminal fragments and it allows quick screening for positive colonies by fluorescence. As a demonstration, eleven cpYFP variants were created and eight showed fluorescence. The emission and excitation spectra of these cpYFP variants showed strong similarity to YFP and therefore can be used in replacement.

Using co-cultures expressing fluorescence resonance energy transfer based protein biosensors to simultaneously image caspase-3 and Ca2+ signaling.

Fluorescence resonance energy transfer (FRET)-based protein biosensors allow the spatial and temporal imaging of signaling events in living cells. However, the simultaneous correlation of multiple events of a signaling pathway is hindered by the spectral cross-talk between fluorescent proteins. Here, we show, for signaling pathways that progress synchronously, multiple events can be correlated by using co-cultures expressing different FRET-based protein biosensors. As a demonstration, we investigated the simultaneous caspase-3 and Ca2+ signaling events involved in cell death of COS-7 cells induced by 10 mM H2O2. Interestingly, this H2O2 stimulus induced synchronous caspase-3 activation and Ca2+ signaling. In parallel to caspase-3 activation, cytosolic Ca2+ concentration, [Ca2+]c, gradually rises to its peak and then slowly drops. As cell shrinkage and rounding ensues, [Ca2+]c again gradually rises to its peak and then reaches a plateau. These observations reveal the relative timing and location of these signaling events in cell death induced by this stimulus of H2O2. Finally, our approach offers an exciting opportunity for spatial and temporal imaging of multiple events in a signaling pathway in living cells.