Detection of mismatched caspase-3 DNA oligonucleotides with an SPR biosensor following amplification by Taq polymerase

Zhang, Ying; Mu, Ying; Zhou, Chao; Song, Qi; Jin, Wei; Jin, Qinhan

doi:10.1007/s00604-012-0799-0

Cited by 6 publications

(1 citation statement)

References 24 publications

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“…The utility of this approach is evident in another study that employed an SPR imaging protein chip system to monitor the caspase-3 activation [98]. In addition, Zhang [106] and Li [107] explored using SPR biosensors and a nonconjugated gold nanoparticlequantum dot pair for detecting mismatched caspase-3 DNA oligonucleotides and caspase-3 activities, respectively.…”

Section: Breakthroughs In Homogeneous Caspase Activity Detectionmentioning

confidence: 99%

A Comprehensive Exploration of Caspase Detection Methods: From Classical Approaches to Cutting-Edge Innovations

Zhra,

Qasem,

Aldossari

et al. 2024

IJMS

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The activation of caspases is a crucial event and an indicator of programmed cell death, also known as apoptosis. These enzymes play a central role in cancer biology and are considered one promising target for current and future advancements in therapeutic interventions. Traditional methods of measuring caspase activity such as antibody-based methods provide fundamental insights into their biological functions, and are considered essential tools in the fields of cell and cancer biology, pharmacology and toxicology, and drug discovery. However, traditional methods, though extensively used, are now recognized as having various shortcomings. In addition, these methods fall short of providing solutions to and matching the needs of the rapid and expansive progress achieved in studying caspases. For these reasons, there has been a continuous improvement in detection methods for caspases and the network of pathways involved in their activation and downstream signaling. Over the past decade, newer methods based on cutting-edge state-of-the-art technologies have been introduced to the biomedical community. These methods enable both the temporal and spatial monitoring of the activity of caspases and their downstream substrates, and with enhanced accuracy and precision. These include fluorescent-labeled inhibitors (FLIs) for live imaging, single-cell live imaging, fluorescence resonance energy transfer (FRET) sensors, and activatable multifunctional probes for in vivo imaging. Recently, the recruitment of mass spectrometry (MS) techniques in the investigation of these enzymes expanded the repertoire of tools available for the identification and quantification of caspase substrates, cleavage products, and post-translational modifications in addition to unveiling the complex regulatory networks implicated. Collectively, these methods are enabling researchers to unravel much of the complex cellular processes involved in apoptosis, and are helping generate a clearer and comprehensive understanding of caspase-mediated proteolysis during apoptosis. Herein, we provide a comprehensive review of various assays and detection methods as they have evolved over the years, so to encourage further exploration of these enzymes, which should have direct implications for the advancement of therapeutics for cancer and other diseases.

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Section: Breakthroughs In Homogeneous Caspase Activity Detectionmentioning

confidence: 99%