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- W2004222794 abstract "The compression process of a single human serum albumin (HSA) molecule by an atomic force microscope (AFM) tip in ultra high vacuum (UHV) condition is studied by the molecular dynamics (MD) simulations with the all-atom empirical force field model. The temperature is assumed to be 0 and 300 K, and the force curves are calculated assuming that both the tip and surface are rigid. At T = 300 K the thermal motion is found to promote the relaxation inside the protein and reduce the normal force observed. Furthermore, the saw-tooth peaks observed in the force curves are found to originate from abrupt structural changes in the sidechains at the atomic level." @default.
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- W2004222794 date "2007-04-01" @default.
- W2004222794 modified "2023-10-14" @default.
- W2004222794 title "Atomistic simulation of compression of single human serum albumin molecule by AFM tip" @default.
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- W2004222794 doi "https://doi.org/10.1088/1742-6596/61/1/222" @default.
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