Abstract

Molecular assembly in a complex cellular environment is vital for understanding underlying biological mechanisms. Biophysical parameters (such as single-molecule cluster density, cluster-area, pairwise distance, and number of molecules per cluster) related to molecular clusters directly associate with the physiological state (healthy/diseased) of a cell. Using super-resolution imaging along with powerful clustering methods (K-means, Gaussian mixture, and point clustering), we estimated these critical biophysical parameters associated with dense and sparse molecular clusters. We investigated Hemaglutinin (HA) molecules in an Influenza type A disease model. Subsequently, clustering parameters were estimated for transfected NIH3T3 cells. Investigations on test sample (randomly generated clusters) and NIH3T3 cells (expressing Dendra2-Hemaglutinin (Dendra2-HA) photoactivable molecules) show a significant disparity among the existing clustering techniques. It is observed that a single method is inadequate for estimating all relevant biophysical parameters accurately. Thus, a multimodel approach is necessary in order to characterize molecular clusters and determine critical parameters. The proposed study involving optical system development, photoactivable sample synthesis, and advanced clustering methods may facilitate a better understanding of single molecular clusters. Potential applications are in the emerging field of cell biology, biophysics, and fluorescence imaging.

Highlights

  • Single-molecule-based live-cell imaging is becoming an essential technique in applied physics, biophysics, and fluorescence microscopy [1,2,3,4,5,6,7,8,9,10,11,12]

  • The following years have observed a surge in several important variants of super-resolution imaging such as individual molecule localization–selective plane illumination microscopy (IML-SPIM) [20], ground state depletion microscopy (GSDIM) [21], super-resolution optical fluctuation imaging (SOFI) [22], points accumulation for imaging in nanoscale topography (PAINT) [23,24], simultaneous multiplane imaging-based localization encoded (SMILE) [9,25], MINFLUX [26], Probabilistic Optically Selective Single-molecule Imaging Based Localization Encoded (POSSIBLE) [6], and other techniques [27,28,29,30,31,32,33,34]

  • The resultant high-resolution images form the basis for understanding biophysical mechanisms and estimating critical statistical parameters related to single-molecule dynamics

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Summary

Introduction

Single-molecule-based live-cell imaging is becoming an essential technique in applied physics, biophysics, and fluorescence microscopy [1,2,3,4,5,6,7,8,9,10,11,12]. The field has grown by leaps and found new applications in diverse research disciplines ranging from single-molecule physics to cell biophysics [13,14,15,16,17,18,19]. The resultant high-resolution images form the basis for understanding biophysical mechanisms and estimating critical statistical parameters related to single-molecule dynamics. This calls for reliable clustering methods and for accurate parameter estimation. Employing an appropriate clustering method is central for understanding molecule clusters in the complex cellular environment

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