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Biology subjects

Mohanan, G.

Publications and source records attributed to Mohanan, G..

5 recordsLinked to original sources

Fluorescence cross-correlation spectroscopy quantifies affinity, cooperativity, and kinetic stability in ternary protein complexes

Many biological processes and emerging therapeutic modalities rely on higher-order protein complexes whose properties cannot be predicted from their constituent binary interactions. However, methods for directly quantifying affinity, cooperativity, and kinetic stability within such assemblies remain limited. Here, we establish fluorescence cross-correlation spectroscopy (FCCS) as a solution-phase approach for characterizing multicomponent protein interactions and apply it to the clinically important HER2-targeting antibodies trastuzumab and pertuzumab. Using fluorescently labelled HER2, trastuzumab, and pertuzumab, we quantified binary binding affinities, directly measured ternary complex formation, and characterized the dissociation kinetics of binary and ternary complexes. FCCS measurements revealed positive cooperativity in the formation of the HER2-trastuzumab-pertuzumab ternary complex, while dissociation experiments demonstrated that the ternary complex is kinetically more stable than the corresponding binary interactions. Together, these findings provide direct solution-phase evidence that cooperative interactions stabilize the HER2-trastuzumab-pertuzumab complex, offering a molecular explanation for the enhanced efficacy of dual HER2 targeting in cancer therapy. More broadly, this work demonstrates that FCCS can robustly quantify affinity, cooperativity, and kinetic stability of multicomponent protein complexes using a commercially available platform. We provide a broadly accessible framework for studying higher-order protein interactions and supporting the development of next-generation multispecific and combination therapeutics. Significance StatementMany proteins function as part of multicomponent complexes, yet most experimental methods characterize interactions only one pair at a time, or indirectly through secondary reporters, or necessitating saturation of binary interactions first. We show that fluorescence cross-correlation spectroscopy can directly quantify how multiple binding partners interact simultaneously by measuring affinity, cooperativity, and kinetic stability in solution. Applying this approach to the clinically important HER2-targeting antibodies trastuzumab and pertuzumab reveals cooperative stabilization of their ternary complex. Because the measurements are performed on a commercially available instrument and require no surface immobilization, this broadly accessible method should facilitate mechanistic studies of complex biomolecular interactions and aid the development of multispecific and combination therapeutics.

biophysics↗

Translation control of autophagy genes upon hydroxyurea-induced genotoxic stress

The fine balance between cellular homeostasis and stress response is crucial for cell survival. In this study, we identify translation regulation of specific autophagy (ATGs) genes by translation repressor Sbp1 upon hydroxyurea-mediated genotoxic stress. Sbp1 localizes to reversible, mRNA-containing granules specifically upon HU stress in RNA recognition motif 1 (RRM1) and RGG motif-dependent manner. Granule localization is independent of eIF4G1 binding despite increased arginine methylation. Deletion of SBP1 increased the tolerance to HU. RNA sequencing of polysome fractions identified ATG1, 2, 9 mRNAs being translationally upregulated in{Delta} sbp1 upon HU stress. Translation of TEL1 and MEC1, the upstream activators of autophagy, also increased in{Delta} sbp1. Concomitantly, increased autophagy and decreased NHEJ repair in{Delta} sbp1 cells was observed. Together, these findings identify Sbp1 as a regulator of the autophagy pathway in response to genotoxic stress by modulating autophagy at two levels, possibly mediated by its ability to localize to granules.

cell biology↗

Automated Purification of DNA Origami with SPRI Beads

DNA origami synthesis is a well-established technique and has been employed in various applications. The synthesised origami must be purified to eliminate the excess materials such as DNA oligos and other molecules. While several purification techniques are routinely used, they all have limitations, and none can be automated to simultaneously handle large numbers and quantities of samples. Here we introduce the use of solid-phase immobilisation (SPRI) beads as an easy-to-adopt, scalable, high-throughput and automation-compatible method to purify DNA origami. Not only can this method remove excess oligos and biomolecules with comparable yield to existing methods while maintaining high structural integrity of the origami, but it also allows an automated workflow to simultaneously purify large numbers of samples within a limited time. We envision that the SPRI beads purification approach will improve the scalability of DNA nanostructures synthesis both for research and commercial applications.

biophysics↗

RGG-motif proteins regulate mRNA translation upon genotoxic stress

Genotoxic stress response (GSR) mediated by mRNA translation and decay regulation remains poorly explored. Here, we identify a unique role of yeast RGG-motif protein Scd6 and its human ortholog LSM14A in mRNA translation control upon hydroxyurea (HU)-mediated GSR. Scd6/LSM14A, but not all tested RGG-containing proteins, localize to HU-induced cytoplasmic puncta in an RGG-dependent manner. The absence of Scd6 increases HU tolerance but sensitizes the cells to HU upon overexpression of SRS2, a known dampener of the DNA- damage response. Scd6 binds SRS2 mRNA to repress its translation in cytoplasmic granules upon HU stress. Scd6-SRS2 interaction is modulated by arginine methylation (AM) and the LSm-domain, which acts as a cis-regulator of Scd6 AM. Polysome-profiling experiments indicate that LSM14A regulates the translation of NHEJ factor mRNAs such as LIG4 (DNL4 homolog) and RTEL1 (SRS2 functional homolog), and the NHEJ activity in response to HU. Overall, this report unveils the role of AM and Scd6/LSM14A in the GSR by determining the translation status of specific mRNAs.

cell biology↗

Nanopore Fingerprinting of Supramolecular DNA Nanostructures

DNA nanotechnology has paved the way for new generations of programmable nanomaterials. Utilising the DNA origami technique, various DNA constructs can be designed, ranging from single tiles to the self-assembly of large-scale complex multi-tile arrays. These DNA nanostructures have enabled new applications in biosensing, drug delivery and other multifunctional materials. In this study, we demonstrate real-time, non-destructive and label-free fingerprinting of higher-order assemblies of DNA origami nanostructures using solid-state nanopores. Using this approach, we quantify the assembly yields for each DNA origami nanostructure with single-entity resolution using the nanostructure-induced charge introduced in the nanopore as a discriminant. We compare the assembly yield of the supramolecular DNA nanostructures obtained with the nanopore with agarose gel electrophoresis and AFM imaging and demonstrate that the nanopore system can provide enhanced information about the nanostructures. We envision that this nanopore detection platform can be applied to a range of nanomaterial designs and enable the analysis and manipulation of large DNA assemblies in real-time with single-molecule resolution. STATEMENT OF SIGNIFICANCEWe demonstrate a single molecule high-throughput approach for the analysis of higher-order DNA origami assemblies with a crowded nanopore. The technique enables the characterisation of DNA origami nanostructures at statistically relevant numbers in real-time and at single-molecule resolution while being non-destructive and label-free, and without the requirement of lengthy sample preparations or use of expensive reagents. We exemplify the technique by demonstrating the quantification of the assembly yield of DNA origami nanostructures based on their equivalent charge surplus computed from the ion current signals recorded. Compared to the standard analysis methods of AFM and agarose gel electrophoresis, the nanopore measurements provides enhanced information about the nanostructures.

biophysics↗