Soluble fibrin (SF) in blood consists of monomers lacking both fibrinopeptides A with a minor population in multimeric clusters. It is a substantial component of isolated fibrinogen (fg), which spontaneously self-assembles into protofibrils progressing to fibers at sub-physiologic temperatures, a process enhanced by adsorption to hydrophobic and some metal surfaces. *
In their article “Novel characteristics of soluble fibrin: hypercoagulability and acceleration of blood sedimentation rate mediated by its generation of erythrocyte-linked fibers” Dennis K. Galanakis, Anna Protopopova, Kao Li, Yingjie Yu, Tahmeena Ahmed, Lisa Senzel, Ryan Heslin, Mohamed Gouda, Jaseung Koo, John Weisel, Marilyn Manco-Johnson and Miriam Rafailovich mention how they employed topographic and lateral atomic force microscopy (AFM) scanning for imaging fg monomers and soluble polymers. Adsorption to polystyrene (PS) and to trioctylmethylamine (TOMA) coated silica wafers was used.
NANOSENSORS™ SuperSharpSilicon™ SSS-SEIHR high resolution AFM probes (typical AFM tip radius of 2 nm, typical force constant 15 N/m, typical resonance frequency 130 kHz) were used for the atomic force microscopy (AFM) in tapping mode. *
*Dennis K. Galanakis, Anna Protopopova, Kao Li, Yingjie Yu, Tahmeena Ahmed, Lisa Senzel, Ryan Heslin, Mohamed Gouda, Jaseung Koo, John Weisel, Marilyn Manco-Johnson and Miriam Rafailovich
Novel characteristics of soluble fibrin: hypercoagulability and acceleration of blood sedimentation rate mediated by its generation of erythrocyte-linked fibers
Cell and Tissue Research 387, pages 479–491 (2022)
DOI: https://doi.org/10.1007/s00441-022-03599-9
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