Published July 20, 2022 | Version v1
Journal article Open

AFM-Based High-Throughput Nanomechanical Screening of Single Extracellular Vesicles

  • 1. Consorzio Interuniversitario per lo Sviluppo dei Sistemi a Grande Interfase, 50019 Firenze, Italy; Consiglio Nazionale delle Ricerche, Istituto per lo Studio dei Materiali Nanostrutturati, 40129 Bologna, Italy; Dipartimento di Chimica "Ugo Schiff", Università degli Studi di Firenze, 50019 Firenze, Italy
  • 2. Consorzio Interuniversitario per lo Sviluppo dei Sistemi a Grande Interfase, 50019 Firenze, Italy; Consiglio Nazionale delle Ricerche, Istituto per lo Studio dei Materiali Nanostrutturati, 40129 Bologna, Italy
  • 3. Consorzio Interuniversitario per lo Sviluppo dei Sistemi a Grande Interfase, 50019 Firenze, Italy; Dipartimento di Chimica "Ugo Schiff", Universitàdegli Studi di Firenze, 50019 Firenze, Italy
  • 4. Consorzio Interuniversitario per lo Sviluppo dei Sistemi a Grande Interfase, 50019 Firenze, Italy; Dipartimento di Medicina Molecolare e Traslazionale, Università degli Studi di Brescia, 25123 Brescia, Italy
  • 5. Department of Clinical Medicine, Faculty of Health, Aarhus University, 8200 Aarhus, Denmark
  • 6. HansaBiomed Life Sciences, 12618 Tallinn, Estonia
  • 7. Department of Biochemistry & Cell Biology, Faculty of Veterinary Medicine, Utrecht University, 3584 CM Utrecht, The Netherlands

Description

The mechanical properties of extracellular vesicles (EVs) are known to influence their biological function, in terms of, e.g., cellular adhesion, endo/ exocytosis, cellular uptake, and mechanosensing. EVs have a characteristic nanomechanical response which can be probed via force spectroscopy (FS) and exploited to single them out from nonvesicular contaminants or to discriminate between subtypes. However, measuring the nanomechanical characteristics of individual EVs via FS is a labor-intensive and time-consuming task, usually limiting this approach to specialists. Herein, we describe a simple atomic force microscopy based experimental procedure for the simultaneous nanomechanical and morphological analysis of several hundred individual nanosized EVs within the
hour time scale, using basic AFM equipment and skills and only needing freely available software for data analysis. This procedure yields a “nanomechanical snapshot” of an EV sample which can be used to discriminate between subpopulations of vesicular and nonvesicular objects in the same sample and between populations of vesicles
with similar sizes but different mechanical characteristics. We demonstrate the applicability of the proposed approach to EVs
obtained from three very different sources (human colorectal carcinoma cell culture, raw bovine milk, and Ascaris suum nematode
excretions), recovering size and stiffness distributions of individual vesicles in a sample. EV stiffness values measured with our highthroughput method are in very good quantitative accord with values obtained by FS techniques which measure EVs one at a time. We show how our procedure can detect EV samples contamination by nonvesicular aggregates and how it can quickly attest the presence of EVs even in samples for which no established assays and/or commercial kits are available (e.g., Ascaris EVs), thus making it a valuable tool for the rapid assessment of EV samples during the development of isolation/enrichment protocols by EV
researchers. As a side observation, we show that all measured EVs have a strikingly similar stiffness, further reinforcing the hypothesis that their mechanical characteristics could have a functional role.

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Additional details

Funding

European Commission
evFOUNDRY - The Extracellular Vesicle Foundry 801367