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| Natura: | Preprint |
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2025
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| Accesso online: | https://arxiv.org/abs/2506.08323 |
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| _version_ | 1866909645055983616 |
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| author | Wang, Hanyang. Slater, Gary W |
| author_facet | Wang, Hanyang. Slater, Gary W |
| contents | Long DNA molecules can be mapped by cutting them with restriction enzymes inside a narrow channel. Once cut, the individual fragments thus produced move away from each other due to diffusion and entropic effects. We investigate how long it takes for these fragments to travel distances large enough for an experimental device to distinguish them and (possibly) estimate their size. In essence, this is a single-file diffusion process in which molecules of different sizes and hence different diffusion coefficients spread out from an initially dense configuration. We use Monte Carlo methods to investigate this class of problems and define the time taken to reach the required final state as a first-passage \textit{spreading time}. Our results demonstrate that the stochastic nature of the diffusion process is as significant as the specifics of the molecular size distribution in determining the spreading time. We examine the relationship between the spreading time and the final space occupied by the fragments as a function of the experimental parameters and determine the fundamental length scale governing this process. We introduce a molecular sequence randomness parameter, $Z$, which is linearly correlated with the final spreading time. Finally, we show that the distribution function of spreading times follows a well-known form for first-passage time problems, and that its variance decreases linearly with the number of fragments. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2506_08323 |
| institution | arXiv |
| publishDate | 2025 |
| record_format | arxiv |
| spellingShingle | Diffusive spreading of a polydisperse polymer solution in a channel Wang, Hanyang. Slater, Gary W Soft Condensed Matter Biological Physics Long DNA molecules can be mapped by cutting them with restriction enzymes inside a narrow channel. Once cut, the individual fragments thus produced move away from each other due to diffusion and entropic effects. We investigate how long it takes for these fragments to travel distances large enough for an experimental device to distinguish them and (possibly) estimate their size. In essence, this is a single-file diffusion process in which molecules of different sizes and hence different diffusion coefficients spread out from an initially dense configuration. We use Monte Carlo methods to investigate this class of problems and define the time taken to reach the required final state as a first-passage \textit{spreading time}. Our results demonstrate that the stochastic nature of the diffusion process is as significant as the specifics of the molecular size distribution in determining the spreading time. We examine the relationship between the spreading time and the final space occupied by the fragments as a function of the experimental parameters and determine the fundamental length scale governing this process. We introduce a molecular sequence randomness parameter, $Z$, which is linearly correlated with the final spreading time. Finally, we show that the distribution function of spreading times follows a well-known form for first-passage time problems, and that its variance decreases linearly with the number of fragments. |
| title | Diffusive spreading of a polydisperse polymer solution in a channel |
| topic | Soft Condensed Matter Biological Physics |
| url | https://arxiv.org/abs/2506.08323 |