System and method for presenting large dna molecules for analysis

Abstract

Systems and methods for presenting nucleic acid molecules for analysis are provided. The nucleic acid molecules have a central portion that is contained within a nanoslit. The nanoslit contains an ionic buffer. The nucleic acid molecule has a contour length that is greater than a nanoslit length of the nanoslit. An ionic strength of the ionic buffer and electrostatic or hydrodynamic properties of the nanoslit and the nucleic acid molecule combining to provide a summed Debye length that is greater than or equal to the smallest physical dimension of the nanoslit.

1 . A micro-fluidic device comprising:
 a first microchannel;   a second microchannel;   a nanoslit extending between the first and second micro channels, the nanoslit providing a fluid path between the first and the second microchannels;   a nucleic acid molecule having a first end portion, a second end portion, and a central portion positioned between the first end portion and the second end portion; and   an ionic buffer within the nanoslit and the first and second microchannel;   the first microchannel including a first cluster region adjacent to a first end of the nanoslit and the second microchannel including a second cluster region adjacent to a second end of the nanoslit, the first cluster region containing the first end portion, the second cluster region containing the second end portion, and the nanoslit containing the central portion,   the nucleic acid molecule having a contour length that is greater than a nanoslit length of the nanoslit, and   an ionic strength of the ionic buffer and electrostatic or hydrodynamic properties of the nanoslit and the nucleic acid molecule combining to provide a summed Debye length that is greater than or equal to a nanoslit height or a nanoslit width, wherein the nanoslit height or nanoslit width is the smallest physical dimension of the nanoslit.   
     
     
         2 . The micro-fluidic device of  claim 1 , wherein the nanoslit has a nanoslit width of less than or equal to 1 μm or a nanoslit height of less than or equal to 100 nm. 
     
     
         3 . The micro-fluidic device of  claim 1 , wherein the nanoslit length is less than or equal to half a contour length of the nucleic acid molecule. 
     
     
         4 . The micro-fluidic device of  claim 1 , wherein at least one of the microchannels has one or more of the following: a microchannel width of about 20 μm, a microchannel length of about 10 mm, and a microchannel height of about 1.66 μm. 
     
     
         5 . The micro-fluidic device of  claim 1 , the device further comprising a temperature adjustment module. 
     
     
         6 . The micro-fluidic device of  claim 1 , wherein the ionic buffer has a temperature of less than or equal to 20° C. 
     
     
         7 . The micro-fluidic device of  claim 1 , wherein the ionic buffer further comprises a viscosity modifier. 
     
     
         8 . The micro-fluidic device of  claim 1 , wherein the nucleic acid molecule has a relaxation time of at least about 30 seconds. 
     
     
         9 . The micro-fluidic device of  claim 1 , wherein the nucleic acid molecule is a DNA molecule. 
     
     
         10 . The micro-fluidic device of  claim 1 , wherein the nucleic acid molecule has a contour length that is at least two times greater than the nanoslit length of the nanoslit. 
     
     
         11 . A method of stretching a nucleic acid molecule in an ionic buffer, the method comprising:
 positioning the nucleic acid molecule such that a central portion of the nucleic acid molecule occupies a nanoslit, a first end portion of the nucleic acid molecule occupies a first cluster region adjacent to a first end of the nanoslit, and a second end portion of the nucleic acid molecule occupies a second cluster region adjacent to a second end of the nanoslit,   the nanoslit, the first cluster region, and the second cluster region including the ionic buffer,   the nucleic acid molecule having a contour length that is greater than a length of the nanoslit, and   an ionic strength of the ionic buffer and electrostatic or hydrodynamic properties of the nanoslit and the nucleic acid molecule combining to provide a summed Debye length that is greater than or equal to a nanoslit height or a nanoslit width, wherein the nanoslit height or nanoslit width is the smallest physical dimension of the nanoslit.   
     
     
         12 . The method of  claim 11 , wherein positioning the nucleic acid molecule includes threading the nucleic acid molecule through the nanoslit. 
     
     
         13 . The method of  claim 11 , wherein positioning the nucleic acid molecule includes electrokinetically driving the central portion of the nucleic acid molecule into the nanoslit. 
     
     
         14 . The method of  claim 11 , wherein the nanoslit has a nanoslit width of less than or equal to 1 μm or a nanoslit height of less than or equal to 100 nm. 
     
     
         15 . The method of  claim 11 , wherein the nanoslit length is less than or equal to half a contour length of the nucleic acid molecule. 
     
     
         16 . The method of  claim 11 , wherein at least one of the microchannels has one or more of the following: a microchannel width of about 20 μm, a microchannel length of about 10 mm, and a microchannel height of about 1.66 μm. 
     
     
         17 . The method of  claim 11 , wherein the ionic buffer has a temperature of less than or equal to 20° C. 
     
     
         18 . The method of  claim 11 , wherein the ionic buffer further comprises a viscosity modifier. 
     
     
         19 . The method of  claim 11 , wherein the nucleic acid molecule has a relaxation time of at least about 30 seconds. 
     
     
         20 . The method of  claim 11 , wherein the nucleic acid molecule is a DNA molecule. 
     
     
         21 . The method of  claim 11 , the method further comprising imaging at least a portion of the central portion.