Method for visualizing the base sequence of nucleic acid polymers

• US 5,106,729 A
• Filed: 07/24/1989
• Issued: 04/21/1992
• Est. Priority Date: 07/24/1989
• Status: Expired due to Fees

• Current Assignee: City College of New York
• Original Assignee: Arizona Board of Regents (University of Arizona)
• Inventors: Philipp, Manfred, Lindsay, Stuart M.
• Primary Examiner(s): Burgess Yarbrough, Amelia
• Assistant Examiner(s): Marschel, Ardin H.
• Application Number:
  US07/384,412
• Time in Patent Office: 1,002 Days
• Field of Search: 435/6, 435/810, 435/91, 536/27, 436/501, 935/77, 935/88, 935/86, 935/87, 250/306, 250/307, 250/311
• US Class Current: 435/6.11
• CPC Class Codes: C07H 19/10 with the saccharide radical esterified by phosphoric or polyphosphoric acids
• CPC Class Codes: C07H 19/20 with the saccharide radical esterified by phosphoric or polyphosphoric acids
• CPC Class Codes: C07H 23/00 Compounds containing boron, silicon, or a metal, e.g. chelates, vitamin B12 esters with inorganic acids C07H11/00; metal salts, see parent compounds
• CPC Class Codes: G01Q 60/10 STM [Scanning Tunnelling Microscopy] or apparatus therefor, e.g. STM probes
• CPC Class Codes: Y10S 435/81 Packaged device or kit
• CPC Class Codes: Y10S 977/853 Biological sample

Abstract

A method for determining and visualizing the base sequence of nucleic acidolymers, especially DNA and RNA, with a scanning probe microscope having a tip, the method including replacing the oxygen in the nucleic acid polymer with sulfur, complexing the sulfur with a metal such as mercury, and passing the tip over the complexed polymer in a scanning path to measure the potential and record the difference in electrical conductivity at preselected increments along the scanning path.

Claims

1. A method for the determination of the nucleotide sequence of DNA and RNA with a scanning probe microscope having a tip, said method comprising:

(a) contacting a DNA or RNA sample with a polymerase in the presence of a sulfur-containing nucleoside 5'"'"'-triphosphate to form an amplified DNA or RNA polymer containing a sulfur-containing nucleotide;

(b) contacting said amplified polymer with a nonchelated soluble organometallic compound to form a metal-complexed nucleic acid polymer;

(c) disposing said metal-complexed nucleic acid polymer on a substrate which is flat to within a few atoms across an area of several square microns;

(d) passing said tip of said scanning microscope in a probe path over the surface of said polymer to measure electrical conductivity or potential therebetween; and

(e) recording the difference in electrical conductivity or potential so measured at preselected increments along said scanning probe path to identify the location of nucleoside bases to determine the sequence of said DNA nucleoside bases.

2. A method according to claim 1 in which said soluble organometallic compound contains a metal selected from the group consisting of mercury, silver, bismuth, cadmium, cerium, cobalt, copper, iron, lanthanum, manganese, nickel, lead, platinum, tin, titanium and zinc.

3. A method according to claim 1 in which said microscope is a scanning-tunnel microscope.

4. A method according to claim 1 in which said microscope is atomic-force microscope.

5. A method for visualizing the base sequence of nucleic acid polymers with a scanning probe microscope having a tip, said method comprising forming a sulfur-containing polynucleotide;

placing said sulfur-containing polynucleotide into a solution containing a soluble mercury compound to complex said mercury-containing compound with the sulfur-containing polynucleotide;

depositing said mercury-complexed nucleic acid polymer on a gold substrate which is flat to within a few atoms over an area of several square microns;

passing the tip of said scanning microscope in a path over the surface of said deposited polymer to measure conductivity or potential therebetween; and

recording the difference in electrical conductivity or electrical potential so measured at preselected increments along said scanning probe path.

6. A method according to claim 5 in which said nucleic acid polymer is selected from the group consisting of DNA and RNA.

7. A method according to claim 6 in which said microscope is a scanning-tunnel microscope.

8. A method according to claim 6 in which said microscope is atomic-force microscope.

9. A method according to claim 5 in which said substrate is prepared by depositing Angstrom amounts of gold epitaxially on freshly cleaned scratch-free mica in an ultra high vacuum system.

10. A method according to claim 9 in which said gold-bearing mica is preheated to about 300°

C. in a oil-free system at least 10^-9 torr, removed from said system, and stored under argon until needed.

11. A method according to claim 5 in which said tip is formed of Pt-Ir wire.

12. A method according to claim 11 in which said tip is pretreated by immersing said tip into a solution of 3M NaCN and 1M NaOH, applying 20 volts of a c to said immersed tip until 0.5 Amperes rms. flows therethrough;

stopping the current flow;

applying small bursts of current to said tip until the lower region thereof parts;

pressing said tip through a film of hard wax preheated to a temperature of from 100°

C. to about 200°

C. to deposit wax on said tip; and

removing said wax-coated tip from said wax.

13. A method for visualizing the base sequence of a nucleic acid polymer selected from the group consisting of DNA and RNA with a scanning tunneling microscope having a tip operatively associated therewith, said method comprising placing said nucleic acid polymer into a solution containing a compound having a sulfur atom capable of replacing the oxygen atom in said polymer;

dissolving said oxygen-reduced polymer in a buffer solution;

depositing said polymer-containing buffer solution in a cell having a gold substrate;

introducing sodium 4-hydroxymercuribenzoate into said cell;

inserting a Pt-Ir wire counter electrode into said cell under a 2 V bias to cause hydrogen to evolve therefrom;

lowering said tip toward said substrate to measure the difference in electrical conductivity at preselected increments thereof along a predefined path; and

translating said differences in electrical conductivity or electrical potential into a visual pattern representing the base sequence of said nucleic acid polymer.

14. A method according to claim 13 in which said compound is a thiophosphate.

15. A method according to claim 14 in which said thiophosphate is alpha 2'"'"'-thio-deoxynucleoside 5'"'"'-triphosphate.

17. A method according to claim 14 in which said cation is mercury.

18. A method according to claim 17 in which said mercury is contained in a soluble mercury salt.

19. A method according to claim 17 in which said mercury is contained in a soluble alkyl mercury compound.

20. A method according to claim 17 in which said mercury is contained in a soluble aryl mercury compound.

16. A method for visualizing the base sequence of nucleic acid polymers with a scanning probe microscope having a tip, the method comprising:

forming a sulfur-containing polynucleotide;

placing said sulfur-containing polynucleotide into a solution containing a soluble cation-containing compound, said cation being selected from the group consisting of mercury, silver, bismuth, cadmium, cerium, cobalt, copper, iron, lanthanum, manganese, nickel, lead, platinum, tin, titanium and zinc, to complex said cation-containing compound with said sulfur-containing polynucleotide;

depositing said cation-complexed nucleic acid polymer on a gold substrate flat to within a few atoms;

passing the tip of said scanning microscope in a path over the surface of said polymer to measure electrical conductivity or electrical potential therebetween; and

recording the difference in electrical conductivity or electrical potential so measured at preselected increments along said scanning probe path.