Methods and arrays for controlled manipulation of DNA and chromatin fragments for genetic and epigenetic analysis

Patent metadata

Field	Value
Publication number	US-9856513-B2
Application number	US-201314374819-A
Country	US
Kind code	B2
Filing date	Jan 28, 2013
Priority date	Jan 27, 2012
Publication date	Jan 2, 2018
Grant date	Jan 2, 2018

Abstract

The present invention relates to methods and arrays for use in high resolution imaging of individual nucleic acid molecules and chromatin fragments, including native chromatin fragments. In one aspect, the present invention relates to a chromatin array that includes a transfer platform having a support and a transfer surface layered on the support. The chromatin array also includes a plurality of elongated individual native chromatin fragments coupled to the transfer surface in an orderly pattern suitable for high resolution imaging of the plurality of native chromatin fragments. The native chromatin fragments of the chromatin array include both DNA and histones.

First claim

What is claimed is:

1. A method of high resolution imaging and analysis of native chromatin, said method comprising:
(a) providing a plurality of native chromatin fragments;
(b) immobilizing the plurality of native chromatin fragments to a transfer platform in an orderly pattern suitable for high resolution imaging of the plurality of native chromatin fragments, wherein said native chromatin fragments comprise both DNA and histones; and
(c) conducting high resolution imaging and analysis of the native chromatin fragments,
wherein the step (b) of immobilizing the plurality of native chromatin fragments to the transfer platform comprises the steps of:
(i) providing a plurality of elongated individual native chromatin fragments removably coupled to a hydrophobic component in an orderly pattern suitable for high resolution imaging of the plurality of native chromatin fragments, wherein said native chromatin fragments comprise both DNA and histones; and
(ii) transferring the plurality of elongated individual native chromatin fragments to a transfer platform, thereby yielding a chromatin array comprising the plurality of elongated individual chromatin fragments attached to the transfer platform in said orderly pattern,
wherein said transfer platform comprises a support and a transfer surface layered on the support;
wherein said transfer platform is effective to receive and capture the plurality of elongated individual chromatin fragments in said orderly pattern from said hydrophobic component; and
wherein the native chromatin fragments are labeled with more than one different type of label for imaging or assaying purposes.

2. The method according to claim 1 , wherein said hydrophobic component comprises a micro/nanostructured capture array comprising a hydrophobic surface having topographical features effective to assist in capillary-based trapping and elongation of individual native chromatin fragments in an orderly pattern.

3. The method according to claim 1 , wherein the labeling comprises either bulk labeling of the native chromatin fragments prior to transferring them to the transfer platform or direct labeling of the native chromatin fragments after transferring them to the transfer platform.

4. The method according to claim 1 , wherein the DNA is labeled, the histones are labeled, or both the DNA and histones are labeled.

5. The method according to claim 1 , wherein said transfer surface is hydrophobic.

6. The method according to claim 5 , wherein the hydrophobic transfer surface is selected from the group consisting of graphene, a graphene blend, a graphene derivative, a graphene-like compound, a thermoplastic, polycarbonate, vinyl, a silanized surface, an elastomer such as polydimethylsiloxane, a metal, a plastic, molybdenum, silicon, silicon nitride, copper, gold, and carbon.

7. The method according to claim 5 , wherein the plurality of elongated individual native chromatin fragments are transferred to the transfer platform using solvent mediation.

8. The method according to claim 1 , wherein said transfer surface is hydrophilic or is functionalized to have a hydrophilic surface.

9. The method according to claim 8 , wherein the hydrophilic transfer surface or functionalized hydrophilic surface thereof is selected from the group consisting of silicon, silicon dioxide (SiO 2 ), glass, mica, a surface functionalized with hydrophilic functional groups, quartz, a silanized surface, and a surface functionalized with hydroxyl groups.

10. The method according to claim 1 , wherein said high resolution imaging comprises techniques selected from the group consisting of optical imaging, optical tweezers technology, fluorescence microscopy, scanning probe microscopy, transmission electron microscopy (TEM), scanning transmission electron microscopy (STEM), electron energy loss spectroscopy (EELS), scanning electron microscopy (SEM), electron tomography, energy-filtered transmission electron microscopy (EFTEM), X-ray spectroscopy, and Auger electron spectroscopy.

11. The method according to claim 1 , wherein said chromatin is from a source selected from the group consisting of a human, a non-human mammal, and a non-mammal.

12. The method according to claim 1 , wherein the elongated chromatin fragments have a length of between about 5 kbp and about 100 kbp and are extended to their contour lengths.

13. The method according to claim 1 , wherein the plurality of immobilized native chromatin fragments are labeled in bulk prior to being immobilized on the transfer platform or labeled individually after being immobilized on the transfer platform.

14. The array according to claim 1 , wherein said native chromatin fragments are coupled to the transfer surface in a beads-on-a-string conformation.

Assignees

• Univ Cornell

Inventors

• Cerf Aline
• Craighead Harold G
• Tian Harvey C

Classifications

• C12Q2522/101

  Single or double stranded nucleic acid binding proteins · CPC title

• G01N1/30

  Staining; Impregnating {; Fixation; Dehydration; Multistep processes for preparing samples of tissue, cell or nucleic acid material and the like for analysis} · CPC title

• C12Q1/6806 Primary

  Preparing nucleic acids for analysis, e.g. for polymerase chain reaction [PCR] assay (C12Q1/6804 takes precedence) · CPC title

• C12Q1/6837 Primary

  using probe arrays or probe chips (C12Q1/6874 takes precedence) · CPC title