Abstract

This study presents an adenosine (A)-based molecular beacon (MB) for selective detection of Naja atra cardiotoxin (CTX) that functions by utilizing the competitive binding between CTX and the poly(A) stem of MB to coralyne. The 5′- and 3′-end of MB were labeled with a reporter fluorophore and a non-fluorescent quencher, respectively. Coralyne induced formation of the stem-loop MB structure through A2-coralyne-A2 coordination, causing fluorescence signal turn-off due to fluorescence resonance energy transfer between the fluorophore and quencher. CTX3 could bind to coralyne. Moreover, CTX3 alone induced the folding of MB structure and quenching of MB fluorescence. Unlike that of snake venom α-neurotoxins, the fluorescence signal of coralyne-MB complexes produced a bell-shaped concentration-dependent curve in the presence of CTX3 and CTX isotoxins; a turn-on fluorescence signal was noted when CTX concentration was ≤80 nM, while a turn-off fluorescence signal was noted with a further increase in toxin concentrations. The fluorescence signal of coralyne-MB complexes yielded a bell-shaped curve in response to varying concentrations of N. atra crude venom but not those of Bungarus multicinctus and Protobothrops mucrosquamatus venoms. Moreover, N. nigricollis venom also functioned as N. atra venom to yield a bell-shaped concentration-dependent curve of MB fluorescence signal, again supporting that the hairpin-shaped MB could detect crude venoms containing CTXs. Taken together, our data validate that a platform composed of coralyne-induced stem-loop MB structure selectively detects CTXs.

Highlights

  • Molecular beacons (MBs) have been widely used as an analytical platform for detecting small biological molecules [1,2]

  • N. nigricollis venom functioned as N. atra venom to yield a bell-shaped concentration-dependent curve of MB fluorescence signal, again supporting that the hairpin-shaped

  • Our data validate that a platform composed of coralyne-induced stem-loop MB structure selectively detects CTXs

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Summary

Introduction

Molecular beacons (MBs) have been widely used as an analytical platform for detecting small biological molecules [1,2]. The on-off fluorescence system could rapidly detect molecules interacting with MB [1,2]. If snake venom proteins could induce ‘turn-on’ or ‘turn-off’ fluorescence signal transduction of MBs, the beacons might be employed for rapid detection of snake venom proteins. Has been thatcould coralyne could (A)‐rich oligonucleotide chain. CTXs could with coralyne for binding the A12with nucleotide insegment the MB in DNA proximity [6].compete. If CTXs could compete with coralynewith for binding the A12 segment nucleotide the probe, separation of FAMofand units units might restore. To test test this hypothesis,the thepresent presentstudy study investigated effect of CTXs onFRET the FRET the MB probe.

Discussion
Fluorescence
Effect fluorescence intensity intensity at at 520
Fluorescence of A
Materials and Methods
Competitive
Binding of Rhodamine-Labeled CTX3 with Coralyne
Molecular Docking
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