Details of research
A Modular Strategy for Tailoring Functional Ribonucleopeptides
A stable complex of a peptide and RNA, ribonucleopeptide (RNP), provides a new framework to construct a macromolecular receptor for small molecules. The RRE (Rev Responsive Element) RNA and the Rev peptide form a structurally well-characterized stable RNP complex that is suitable for molding of a ligand-binding pocket of the RNP in a step-wise manner.
The first step involves molding of the RNA subunit by in vitro selection of an RNP pool originating from an RNA library and the Rev peptide. The second step involves selection from an RNP library consisting of Rev peptides with randomized amino-acid residues and the RNA subunit selected in the first molding. Together, these steps afford an expanded ligand-binding surface consisting of both RNA and peptide subunits. We report here a step-wise molding strategy to tailor an ATP-binding pocket in the RNP. The ATP-binding pocket produced by sequential molding of RNA and peptide subunits shows higher affinity and specificity to ATP than the ATP-binding RNP receptor in which only the RNA subunit was molded. In vitro selection of the RNP pool originating from an RRE-based RNA library and the Rev peptide affords RNP receptors specific for nucleotide triphosphates or the phosphotyrosine residue.
The peptide-based molding of the ATP-binding RNP was carried out next by using a peptide-derived RNP library constructed by the phage display technique along with an RNA subunit of the ATP-binding RNP obtained from the first RNA-based library selection. An LpRev peptide was designed to possess seven randomized amino-acids (Cys-X7-Cys) at the N-terminus of Rev to facilitate efficient formation of a binding surface. The random LpRev peptides were expressed at the amino terminus of the pIII protein of the filamentous bacteriophage, and expected to form a loop structure upon disulfide bond formation. Phages from the LpRev library were pooled and mixed with the RNA obtained in the first molding step to form a library of RNPs before starting selection against ATP-agarose resin. One of the RNP bearing the LpRev peptide shows higher affinity and selectivity to ATP over dATP than the parent ATP-binding RNP.
A schematic illustration shows the step-wise molding strategy to generate ribonucleopeptide (RNP) receptors for ATP. The first molding step utilizes in vitro selection of an RNP library originating from a randomized RNA nucleotide pool (RRE30N). Combination of the RNA subunit of RNP selected in the first molding and a phage peptide library of the Rev peptide containing seven randomized amino-acid residues affords a peptide-diverged RNP library, which enables the selection in the second molding step of improved ATP-binding RNPs.
The RNP receptor functionalized by a fluorophore-labeled Rev peptide exerts optical signals associated with the ligand binding events. Replacing the Rev peptide of the ATP-binding RNP with a fluorophore-modified Rev peptide affords a series of fluorescent ATP sensors. This strategy to generate tailor-made fluorescent sensors is applied for a selective detection of a specific phosphorylated tyrosine residue within a defined amino acid sequence.
A new strategy for tailoring fluorescent biosensors. Fluorescent biosensors that facilitate reagentless sensitive detection of small molecules are crucial tools in the areas of therapeutics and diagnostics. However, construction of fluorescent biosensors with desired characteristics, i.e., detection wavelengths and concentration ranges for ligand detection, from macromolecular receptors is not a straightforward task. An ATP-binding RNP receptor was converted to a fluorescent ATP sensor without chemically modifying the nucleotide in the ATP-binding RNA. The RNA subunit of the ATP-binding RNP and a peptide modified with a pyrenyl group formed a stable fluorescent RNP complex that showed an increase in the fluorescence intensity upon binding to ATP.
A scheme illustrates a direct conversion of a ribonucleopeptide (RNP) receptor to a fluorescent RNP sensor. A complex of the Rev peptide and RRE RNA was used as a framework for the RNP receptor and RNP sensor.
A simple screening scheme based on the relative changes in emission intensities
of fluorescent RNPs with or without the ligand ATP (I/I0) is quite useful
for the screen of RNP sensors with desired emission wavelength and with high
I/I0 ratio with emission wavelengths varying from 390 to 670 nm. Screening
of the fluorescence emission intensity changes in the presence of increasing
concentrations of ATP allowed titration analysis of the fluorescent RNP library,
which provided ATP sensors responding at wide concentration ranges of ATP.
Simultaneous application of these four sensors covers ATP concentration ranges
from ~10-7 to ~10-2 M.
(A) A scanned image showing the microplate assay for the combinatorial screening of the fluorescent RNP library. Fluorescence intensities of 7mC-Rev derived RNPs (1 μM) were evaluated in the absence or presence of 1 mM of ATP with excitation at 355 nm and emission 390 nm with intensities being weak in blue color and strong in red..
(B) Relative fluorescence intensity changes (I/I0) of RNPs upon ATP binding are shown in the bar graphs for (a) 7mC-Rev RNP, (b) Pyr-Rev RNP, (c) NBD-Rev RNP, and (d) Cy5-Rev RNP.
Saturation curves of 7mC-Rev RNPs A02/7mC-Rev (filles circles), A35/7mC-Rev (filled squares), and A26/7mC-Rev (filled triangles) in the presence of 10 nM to 10 mM ATP were determined by titrations of fluorescence intensity changes.
Context-Dependent Fluorescence Detection of a Phosphorylated Tyrosine Residue by a Ribonucleopeptide
Tools for selective recognition and sensing of specific phosphorylated tyrosine residues on the protein surface are essential for understanding signal transduction cascades in the cell. In vitro selection of an RNA-derived pool of RNP afforded RNP receptors specific for a phosphotyrosine residue within a defined amino-acid sequence Gly-Tyr-Ser-Arg. The RNP receptor for the specific phosphotyrosine residue was successfully converted to a fluorescent RNP sensor for sequence-specific recognition of a phosphorylated tyrosine. The fluorescent RNP sensor has an ability to function as a specific fluorescent sensor for the phosphorylated tyrosine residue within a defined amino-acid sequence in HeLa cell extracts.
Strategy to obtain RNP fluorescent sensors specific for a phosphotyrosine-containing amino acid sequence GpYSR. Combination of the RNA subunit of the GpYSR-binding RNP and a fluorophore-modified Rev peptide provided a GpYSR RNP fluorescent sensor.
Development of Fluorescent Ribonucleopeptide Sensors for Histamine
Biologically active amines, such as dopamine, histamine, and serotonin, play major roles in the regulation of movement and are implicated in the pathophysiology of Parkinson’s and Huntington’s diseases, psychosis, and drug addiction. We developed fluorescent RNP sensors for histamine with a variety of binding and signal-transducing characteristics. The fluorescent histamine sensor showed distinct selectivity for histamine over structurally related histamine analogs, such as imidazole, ethylamine and L-histidine.
A strategy to obtain RNP fluorescent sensors specific for histamine. Combination of the RNA subunits of the histamine-binding RNP receptor and a fluorophore-modified Rev peptide provided a histamine RNP fluorescent sensor.
These researches were supported by a Grant-in-aid for Scientific Research from Ministry of Education, Science, Sports and Culture, Japan to T.M. (No. 19021023, and No. 20241051).
Structual Aspects for the Recognition of ATP by Ribonucleopeptide Receptors
Rational design of the functional RNPs would be possible by understanding the structural aspects for the function of RNP receptor. A combination of NMR measurements, enzymatic and chemical mapping, and nucleotide mutation studies of the RNP-adenosine complex show that RNP interacts with the adenine ring of adenosine by forming a U:A:U triple with two invariant U nucleotides (Figure 1b). The observed recognition mode for the adenine ring is very different from those of RNA aptamers for ATP derivatives reported by others previously. The RNP-adenosine complex is folded into a particular structure by formation of the U:A:U triple and a Hoogsteen type A:U base pair (Figure 1b). This recognition mechanism was successfully utilized to convert the substrate-binding specificity of RNP from ATP- to GTP-binding with a C+:G:C triple recognition mode.
(a) A scheme shows the stepwise construction of RNP receptors and fluorescent RNP sensors.
(b) An illustration shows the proposed recognition mode of ATP-binding RNP receptor clarified in this study.