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Cell Rheology Using Atomic Force Microscopy

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dc.contributor.advisor PATIL, SHIVPRASAD
dc.contributor.author JAIMINI, ANSH
dc.date.accessioned 2025-12-17T03:58:04Z
dc.date.available 2025-12-17T03:58:04Z
dc.date.issued 2025-12
dc.identifier.citation 69 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/10579
dc.description MS Thesis en_US
dc.description.abstract This thesis develops and validates a reproducible workflow for AFM cell rheology that adapts the open-source PyFMLab suite to JPK NanoWizard 2 force–indentation datasets and bench- marks it against a vetted MATLAB implementation. A central contrast is methodological: PyFMLab uses an analytical (closed-form) Ting contact solution, whereas the MATLAB workflow evaluates Ting’s model numerically on the same curves. Four predefined MEF cohorts—wild type, Dyna- sore (dynamin inhibition), Y–27632 (ROCK inhibition), and the dual treatment—are analyzed exactly as provided; wet-lab execution is out of scope, and biology is included only for naming and interpretation. Raw deflection and base-piezo signals are converted to force and indentation using a stan- dardized calibration. Curves then pass objective goodness-of-fit screens and quick visual checks before full-cycle linear viscoelastic fitting with power-law relaxation to estimate two compact parameters: the instantaneous modulus E0 and a fluidity exponent. Three candidate inclusion criteria were tested across sessions; after reviewing edge cases, a stringent rule was fixed for primary MATLAB reporting to prioritize high-reliability curves. Results are summarized at curve and cell levels using descriptive statistics, box-and-whisker plots, and omnibus nonparametric tests with corrected post hoc contrasts, enabling transparent cross-tool comparison of E0 and the exponent. Both pipelines support the same qualitative bi- ology: ROCK inhibition shows the largest increase in fluidity, the dual treatment is elevated, and Dynasore remains near WT; stiffness trends are consistent with softening under ROCK inhibition within the probed window. Rather than exact numerical parity, the side-by-side anal- ysis reveals systematic offsets attributable to implementation choices, including the solution method for Ting’s model (analytical vs. numerical), the PLR kernel form, the fitting domain (force–indentation vs. force–time), contact detection/initialization, residual weighting and win- dowing, optimizer settings, and QC retention. In practice, PyFMLab delivers markedly faster throughput and, beyond quasi-static indentation, supports in-contact dynamic microrheology, whereas the MATLAB workflow used here focuses on quasi-static cycles. The study motivates harmonized preprocessing, explicit configuration reporting, and clear QC criteria for repro- ducible, interpretable AFM viscoelastic readouts. en_US
dc.language.iso en en_US
dc.subject Research Subject Categories::NATURAL SCIENCES en_US
dc.subject Research Subject Categories::TECHNOLOGY en_US
dc.subject Research Subject Categories::INTERDISCIPLINARY RESEARCH AREAS en_US
dc.title Cell Rheology Using Atomic Force Microscopy en_US
dc.type Thesis en_US
dc.description.embargo One Year en_US
dc.type.degree BS-MS en_US
dc.contributor.department Dept. of Physics en_US
dc.contributor.registration 20201126 en_US


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  • MS THESES [1980]
    Thesis submitted to IISER Pune in partial fulfilment of the requirements for the BS-MS Dual Degree Programme/MSc. Programme/MS-Exit Programme

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