4.8 Article

Combing of Genomic DNA from Droplets Containing Picograms of Material

期刊

ACS NANO
卷 9, 期 1, 页码 809-816

出版社

AMER CHEMICAL SOC
DOI: 10.1021/nn5063497

关键词

molecular combing; DNA mapping; fiber-FISH; DNA deposition; rolling droplet; coffee ring effect; single-molecule imaging

资金

  1. Department of Chemistry (KU Leuven) the 'Agentschap voor Innovatie door wetenschap en Technologie'
  2. Fonds Wetenschappelijk Onderzoek
  3. European Research Council under the European Union [291593 FLUOROCODE]
  4. Flemish government [METH/08/04 CASAS]
  5. 'Fonds voor Wetenschappelijk Onderzoek Vlaanderen' (FWO) [G.0197.11, G0484.12]
  6. Hercules Foundation [HER/08/021]
  7. FWO [G.0697.11]

向作者/读者索取更多资源

Deposition of linear DNA molecules is a critical step in many single-molecule genomic approaches including DNA mapping, fiber-FISH, and several emerging sequencing technologies. In the ideal situation, the DNA that is deposited for these experiments is absolutely linear and uniformly stretched, thereby enabling accurate distance measurements. However, this is rarely the case, and furthermore, current approaches for the capture and linearization of DNA on a surface tend to require complex surface preparation and large amounts of starting material to achieve genomic-scale mapping. This makes them technically demanding and prevents their application in emerging fields of genomics, such as single-cell based analyses. Here we describe a simple and extremely efficient approach to the deposition and linearization of genomic DNA molecules. We employ droplets containing as little as tens of picograms of material and simply drag them, using a pipet tip, over a polymer-coated coverslip. In this report we highlight one particular polymer, Zeonex, which is remarkably efficient at capturing DNA. We characterize the method of DNA capture on the Zeonex surface and find that the use of droplets greatly facilitates the efficient deposition of DNA. This is the result of a circulating flow in the droplet that maintains a high DNA concentration at the interface of the surface/solution. Overall, our approach provides an accessible route to the study of genomic structural variation from samples containing no more than a handful of cells.

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