Transition and Regulation of MicroRNA Let-7a Conformation at the Membrane Interface by Different Ionic Solutions.

J Phys Chem B

School of Optoelectronic Materials and Technology, & Key Laboratory of Optoelectronic Chemical Materials and Devices, Ministry of Education, Jianghan University, Wuhan 430056, China.

Published: August 2025


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Article Abstract

The Lethal 7 (Let-7) miRNA family is attracting more and more attention in recent decades due to its capability in post-transcriptional regulation and the modulation of various physiological and pathological processes. Yet, the underlying mechanism that controls the conformation and biofunctions of Let-7 molecules during their translocation in and out of the cell membrane is still elusive. In the present study, the sum frequency generation vibrational spectroscopy (SFG-VS), a second-order nonlinear spectroscopic technique, was applied to examine the interfacial behavior of Let-7a at the lipid membrane interface. By creating the lamellar membrane environment with different ionic solutions, we were able to capture conformational changes in the Let-7a molecule based on the SFG spectra collected from the membrane interface after the miRNA-membrane interaction. Our results indicate that the ribose guanosine (rG) residues and ribose uridine (rU) residues of the Let-7a molecule show versatile changes as the concentration of ionic solutions increases. The analysis results also indicate that the hydrogen-bonding networks around the Let-7a molecules are greatly changed by the salt as the concentration of the NaCl and CaCl solutions increases. As NaCl and CaCl solution concentrations rose during experiments, we noted a marked reconfiguration of the hydrogen-bonding network around Let-7a molecules, driven by strengthened interactions between salt ions, water molecules, and Let-7a's functional groups, disrupting the original network and altering its connectivity/stability. This research offers valuable molecular-level insights into the salt-dependent conformation and behavior changes of miRNA at the lamellar lipid membrane interface. These findings also provide new perspectives for miRNA-related therapy and may help researchers in the improvement of innovative and pertinent drug delivery systems.

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http://dx.doi.org/10.1021/acs.jpcb.5c01379DOI Listing

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