Literature DB >> 22098697

Homogeneous single-label biochemical Ras activation assay using time-resolved luminescence.

Eija Martikkala, Stefan Veltel, Jonna Kirjavainen, Anita Rozwandowicz-Jansen, Urpo Lamminmäki, Pekka Hänninen, Harri Härmä.   

Abstract

Mutations of the small GTP-binding protein Ras have been commonly found in tumors, and Ras oncogenes have been established to be involved in the early steps of cancerogenesis. The detection of Ras activity is critical in the determination of the cell signaling events controlling cell growth and differentiation. Therefore, development of improved methods for primary screening of novel potential drugs that target small GTPase or their regulators and their signaling pathways is important. Several assays have been developed for small GTPases studies, but all these methods have limitations for a high-throughput screening (HTS) use. Multiple steps including separation, use of radioactive labels or time-consuming immunoblotting, and a need of large quantities of purified proteins are decreasing the user-friendliness of these methods. Here, we have developed a homogeneous H-Ras activity assay based on a single-label utilizing the homogeneous quenching resonance energy transfer technique (QRET). In the QRET method, the binding of a terbium-labeled GTP (Tb-GTP) to small GTPase protein H-Ras protects the signal of the label from quenching, whereas the signal of the nonbound fraction of Tb-GTP is quenched by a soluble quencher. This enables a rapid determination of the changes in the activity status of Ras. The assay optimization showed that only 60 nM concentration of purified H-Ras protein was needed. The functionality of the assay was proved by detecting the effect of H-Ras guanine nucleotide exchange factor, Son of Sevenless. The signal-to-background ratio up to 7.7 was achieved with an average assay coefficient of variation of 9.1%. The use of a low concentration of purified protein is desirable and the signal-to-background ratio of 3.4 was achieved in the assay at a concentration of 60 nM for H-Ras and SOS proteins. The need of only one labeled molecule and the ability to decrease the quantities of purified proteins used in the experiments are valuable qualities in HTS showing the potential of the QRET method.

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Year:  2011        PMID: 22098697     DOI: 10.1021/ac202723h

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  2 in total

1.  Homogeneous single-label cGMP detection platform for the functional study of nitric oxide-sensitive (soluble) guanylyl cyclases and cGMP-specific phosphodiesterases.

Authors:  Kari Kopra; Iraida Sharina; Emil Martin; Harri Härmä
Journal:  Sci Rep       Date:  2020-10-15       Impact factor: 4.379

2.  Label-Free Time-Gated Luminescent Detection Method for the Nucleotides with Varying Phosphate Content.

Authors:  Kari Kopra; Tanja Seppälä; Dana Rabara; Maria Abreu-Blanco; Sakari Kulmala; Matthew Holderfield; Harri Härmä
Journal:  Sensors (Basel)       Date:  2018-11-16       Impact factor: 3.576

  2 in total

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