Nanopore-based single DNA molecule characterization, identification and isolation using speed bumps
View Patent ↗The present invention relates to a method of using nanopores to obtain sequence information of sample DNAs in ss test DNAs. The method comprises using speed bumps to stall the ss test DNAs in the nanopores at random positions of the ss test DNAs to obtain sequence information of each and every nucleotides of the sample DNAs, and to construct the whole sequences of the sample DNAs. The present invention also relates to identification and/or isolation of test DNAs having desired sequence(s) using nanopore detectors facilitated by speed bump.
1. A method for sequencing a nucleic acid molecule, the method comprising:
applying a first electric potential having a first polarity across an array of nanopore detectors, each nanopore detector comprising a pair of electrodes, a membrane disposed between the pair of electrodes, and a nanopore disposed in the membrane;
threading a plurality of single stranded nucleic acid molecules through the array of nanopore detectors in a first direction based on the first polarity of the applied first electric potential;
measuring a first electrical signal in each nanopore detector as the single stranded nucleic acid molecule is threaded through the nanopore in the first direction;
applying a second electric potential having a second polarity across the array of nanopore detectors, wherein the second polarity is opposite the first polarity;
threading the plurality of single stranded nucleic acid molecules through the array of nanopore detectors in a second direction based on the second polarity of the applied second electrical potential, wherein the second direction is opposite the first direction, wherein each single stranded nucleic acid molecule has a first end comprising a first bulky structure, wherein each single stranded nucleic acid molecule has a second end comprising a second bulky structure, wherein the second end is the leading end of the single stranded nucleic acid molecule and the second bulky structure is configured to prevent the nucleic acid from passing completely through the nanopore when the single stranded nucleic acid is threaded through the nanopore in the second direction, wherein the first bulky structure and the second bulky structures are configured to be converted to non-bulky structures at different working temperatures that will allow the single stranded nucleic acid molecule to pass through the nanopore;
measuring a second electrical signal in each nanopore detector as the single stranded nucleic acid molecule is threaded through the nanopore in the second direction; and
determining a sequence for each single stranded nucleic acid molecule based on the first electrical signal and the second electrical signal.
2. The method of claim 1 , wherein the first end is a trailing end of the single stranded nucleic acid molecule and the first bulky structure is configured to prevent the nucleic acid from passing completely through the nanopore when the single stranded nucleic acid is threaded through the nanopore in the first direction.
3. The method of claim 1 , wherein each single stranded nucleic acid molecule comprises a plurality of speed bumps located along a length of the single stranded nucleic acid molecule, wherein the plurality of speed bumps are configured to slow the threading of the single stranded nucleic acid molecule through the nanopore.
4. A method for sequencing a nucleic acid, the method comprising:
applying a first electric potential having a first polarity across an array of nanopore detectors, each nanopore detector comprising a pair of electrodes, a membrane disposed between the pair of electrodes, and a nanopore disposed in the membrane;
threading a plurality of single stranded nucleic acid molecules through the array of nanopore detectors in a first direction based on the first polarity of the applied first electric potential;
measuring a first electrical signal in each nanopore detector as the single stranded nucleic acid molecule is threaded through the nanopore in the first direction;
applying a second electric potential having a second polarity across the array of nanopore detectors, wherein the second polarity is opposite the first polarity;
threading the plurality of single stranded nucleic acid molecules through the array of nanopore detectors in a second direction based on the second polarity of the applied second electrical potential, wherein the second direction is opposite the first direction, wherein each single stranded nucleic acid molecule has a first end comprising a first bulky structure, wherein each single stranded nucleic acid molecule has a second end comprising a second bulky structure, wherein the second end is the leading end of the single stranded nucleic acid molecule and the second bulky structure is configured to prevent the nucleic acid from passing completely through the nanopore when the single stranded nucleic acid is threaded through the nanopore in the second direction, wherein the first bulky structure and the second bulky structures are configured to be converted to non-bulky structures at different working temperatures that will allow the single stranded nucleic acid molecule to pass through the nanopore;
measuring a second electrical signal in each nanopore detector as the single stranded nucleic acid molecule is threaded through the nanopore in the second direction;
applying a third electrical potential across the array of nanopore detectors, wherein the third electrical potential has a polarity that is the same as the polarity of the first electrical potential;
threading the plurality of single stranded nucleic acid molecules through the array of nanopore detectors in the first direction based on the polarity of the third electrical potential;
measuring a third electrical signal in each nanopore detector as the single stranded nucleic acid molecule is threaded through the nanopore in the first direction as a result of the application of the third electrical potential;
determining a sequence for each single stranded nucleic acid molecule based on any combination of the first electrical signal, the second electrical signal, and the third electrical signal.
5. The method of claim 4 , wherein the first end is a trailing end of the single stranded nucleic acid molecule and the first bulky structure is configured to prevent the nucleic acid from passing completely through the nanopore when the single stranded nucleic acid is threaded through the nanopore in the first direction.
6. The method of claim 4 , wherein each single stranded nucleic acid molecule comprises a plurality of speed bumps located along a length of the single stranded nucleic acid molecule, wherein the plurality of speed bumps are configured to slow the threading of the single stranded nucleic acid molecule through the nanopore.
7. A system for sequencing a nucleic acid molecule, the system comprising:
an array of nanpore detectors, each nanopore detector comprising a pair of electrodes, a membrane disposed between the pair of electrodes, and a nanopore disposed in the membrane;
a controller configured to:
apply a first electric potential having a first polarity across the array of nanopore detectors;
thread a plurality of single stranded nucleic acid molecules through the array of nanopore detectors in a first direction based on the first polarity of the applied first electric potential;
measure a first electrical signal in each nanopore detector as the single stranded nucleic acid molecule is threaded through the nanopore in the first direction;
apply a second electric potential having a second polarity across the array of nanopore detectors, wherein the second polarity is opposite the first polarity;
thread the plurality of single stranded nucleic acid molecules through the array of nanopore detectors in a second direction based on the second polarity of the applied second electrical potential, wherein the second direction is opposite the first direction; and
measure a second electrical signal in each nanopore detector as the single stranded nucleic acid molecule is threaded through the nanopore in the second direction, wherein each single stranded nucleic acid molecule has a first end comprising a first bulky structure, wherein each single stranded nucleic acid molecule has a second end comprising a second bulky structure, wherein the second end is the leading end of the single stranded nucleic acid molecule and the second bulky structure is configured to prevent the nucleic acid from passing completely through the nanopore when the single stranded nucleic acid is threaded through the nanopore in the second direction, wherein the first bulky structure and the second bulky structures are configured to be converted to non-bulky structures at different working temperatures that will allow the single stranded nucleic acid molecule to pass through the nanopore; and
a processor configured to determine a sequence for each single stranded nucleic acid molecule based on the first electrical signal and the second electrical signal.
8. A system for sequencing a nucleic acid molecule, the system comprising:
an array of nanpore detectors, each nanopore detector comprising a pair of electrodes, a membrane disposed between the pair of electrodes, and a nanopore disposed in the membrane;
a controller configured to:
apply a first electric potential having a first polarity across the array of nanopore detectors;
thread a plurality of single stranded nucleic acid molecules through the array of nanopore detectors in a first direction based on the first polarity of the applied first electric potential;
measure a first electrical signal in each nanopore detector as the single stranded nucleic acid molecule is threaded through the nanopore in the first direction;
apply a second electric potential having a second polarity across the array of nanopore detectors, wherein the second polarity is opposite the first polarity;
thread the plurality of single stranded nucleic acid molecules through the array of nanopore detectors in a second direction based on the second polarity of the applied second electrical potential, wherein the second direction is opposite the first direction;
measure a second electrical signal in each nanopore detector as the single stranded nucleic acid molecule is threaded through the nanopore in the second direction, wherein each single stranded nucleic acid molecule has a first end comprising a first bulky structure, wherein each single stranded nucleic acid molecule has a second end comprising a second bulky structure, wherein the second end is the leading end of the single stranded nucleic acid molecule and the second bulky structure is configured to prevent the nucleic acid from passing completely through the nanopore when the single stranded nucleic acid is threaded through the nanopore in the second direction, wherein the first bulky structure and the second bulky structures are configured to be converted to non-bulky structures at different working temperatures that will allow the single stranded nucleic acid molecule to pass through the nanopore;
apply a third electrical potential across the array of nanopore detectors, wherein the third electrical potential has a polarity that is the same as the polarity of the first electrical potential;
thread the plurality of single stranded nucleic acid molecules through the array of nanopore detectors in the first direction based on the polarity of the third electrical potential;
measure a third electrical signal in each nanopore detector as the single stranded nucleic acid molecule is threaded through the nanopore in the first direction as a result of the application of the third electrical potential; and
a processor configured to determine a sequence for each single stranded nucleic acid molecule based on any combination of the first electrical signal, the second electrical signal, and the third electrical signal.