IP Library Granted Patent US 11,016,057
Granted Patent B2
US 11,016,057 · App. 15/634,846 · Granted May 25, 2021

Pulse-field multiplex capillary electrophoresis system

Inventors: Mark R. Ver Meer (Des Moines, IA); Jolita J. Uthe (Ames, IA); Wei Wei (Ames, IA); Martin Chris Foster (Nevada, IA); Bruce R. Boeke (Ames, IA)
Assignee: Agilent Technologies, Inc.
G01N27/44713C12N15/1093C12Q1/6806G01N27/44704G01N27/44721G01N27/44743G01N27/44782G01N27/44791
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Quick Facts
Patent No.
US 11,016,057
App. No.
15/634,846
Granted
May 25, 2021
Kind
B2
Abstract

The invention is a multiplex, pulsed-field capillary electrophoresis instrument with the ability to analyze DNA fragments with sizes greater than 150,000 base pairs. The parallel capillary electrophoresis system allows for the simultaneous analysis of at least 12 samples while applying a pulse or varying electric field for separation. Sequences of pulse-field electric fields are iterated to achieve accurate separation of DNA smears.

Claims (45)

1. A method for multiplex capillary electrophoresis, the method comprising:

applying a sequence of waveforms by:

applying a first pulse-field waveform at a first frequency across each of two capillaries for a first period of time, each of the two capillaries containing molecular species in a medium; and

applying at least a second, different shape pulse-field waveform at a second frequency across each of the two capillaries for a second period of time immediately following the first period of time;

repeating the applying of the sequence of waveforms at least twice; and

detecting and identifying the molecular species in each of the two capillaries from molecular species migration within each of the two capillaries.

2. The method of claim 1 , wherein said first frequency varies with time within said first period of time and said second frequency varies with time within said second period of time.

3. The method of claim 1 , wherein the first pulse-field waveform and the second pulse-field waveform are selected from the group consisting of: a square wave; a triangle wave; a sine wave; and a sawtooth wave.

4. The method of claim 1 , wherein the first period of time and the second period of time are selected from the group consisting of: less than 10 minutes each; less than 5 minutes each; and less than 1 minute each.

5. The method of claim 1 , comprising detecting a sample in windows of said capillaries by fluorescence or absorption detection.

6. The method of claim 1 , wherein the first frequency and the second frequency vary in a range selected from the group consisting of: 0.5 Hz to 100 Hz; 0.5 Hz to 15 Hz; 0.5 Hz to 30 Hz; 2 Hz to 20 Hz; and 2 Hz to 15 Hz.

7. The method of claim 1 , wherein the first pulse-field waveform and the second pulse-field waveform are effective to electrophoretically separate nucleic acids of the sample having fragment sizes greater than 150,000 base pairs (bp) in the capillary array.

8. The method of claim 1 , comprising a feature selected from the group consisting of:

the first pulse-field waveform and the second pulse-field waveform are applied across each of twelve capillaries containing molecular species, wherein the molecular species in each of the twelve capillaries are detected and identified; and

the first pulse-field waveform and the second pulse-field waveform are applied across each of twenty-four capillaries containing molecular species, wherein the molecular species in each of the twenty-four capillaries are detected and identified.

9. A method of multiplex capillary electrophoresis, comprising:

applying a sequence of waveforms by:

applying a first pulse-field waveform at a first frequency across each of two capillaries for a first period of time, each of the two capillaries containing molecular species in a medium;

applying a second, different shape pulse-field waveform across each of the two capillaries at a second frequency for a second period of time immediately following the first period of time; and

applying at least a third pulse-field waveform across each of the two capillaries at a third frequency for a third period of time, the third pulse-field waveform having a shape different from at least one of the first pulse-field waveform or the second pulse-field waveform;

repeating the applying of the sequence of waveforms at least twice; and

detecting and identifying the molecular species in each of the two capillaries from molecular species migration within each of the two capillaries.

10. The method of claim 9 , wherein said first frequency varies with time within said first period of time, said second frequency varies with time within said second period of time, and said third frequency varies with time within said third period of time.

11. A multiplex capillary electrophoresis system for multiplex pulse-field electrophoresis, the multiplex capillary electrophoresis system comprising:

a console configured to house a replaceable capillary array comprising two capillaries;

a pulse-field alternating current power supply disposed in the console; and

a control device configured to control the pulse-field alternating current power supply to:

apply a sequence of waveforms by:

applying a first pulse-field waveform at a first frequency across each of at least two capillaries for a first period of time; and

applying at least a second, different shape pulse-field waveform at a second frequency across each of the two capillaries for a second period of time immediately following the first period of time, and

repeat the applying of the sequence of waveforms at least twice; and

a detector disposed in the console, and configured to detect molecular species in each of the two capillaries from molecular species migration within each of the two capillaries.

12. The multiplex capillary electrophoresis system of claim 11 , wherein the console comprises an injection position under which the capillary array is received, and the console is configured to receive a sample plate at the injection position, the sample plate configured to contain a sample that comprises the molecular species, wherein:

the console is configured to, at the injection position, inject a sample into the capillary array; and

the pulse-field alternating current power supply is configured to, after injection of the sample, apply the first pulse-field waveform and the second pulse-field waveform to effect electrophoretic separation of the sample.

13. The multiplex capillary electrophoresis system of claim 12 , wherein, at the injection position, the pulse-field alternating current power supply is configured to, before applying the first pulse-field waveform and the second pulse-field waveform, apply an electric field effective to inject the sample into the capillary array.

14. The multiplex capillary electrophoresis system of claim 12 , wherein the console is configured to inject the sample hydrodynamically.

15. The multiplex capillary electrophoresis system of claim 11 , comprising:

at least two drawers disposed in the console, and configured to contain separately at least a buffer plate and a sample plate; and

a motion control system disposed in the console, and configured to move at least one of the sample plate or the buffer plate from at least one of the at least two drawers to an injection position of the multiplex capillary electrophoresis system.

16. The multiplex capillary electrophoresis system of claim 11 , wherein the pulse-field alternating current power supply is configured to apply at least a third pulse-field waveform across each of the two capillaries at a third frequency for a third period of time.

17. The multiplex capillary electrophoresis system of claim 11 , comprising a waveform generator communicating with the pulse-field alternating current power supply, and configured to generate the first pulse-field waveform and the second pulse-field waveform.

18. The multiplex capillary electrophoresis system of claim 11 , comprising a capillary array circuit board communicating with the pulse-field alternating current power supply, wherein the pulse-field alternating current power supply is configured to apply the first pulse-field waveform and the second pulse-field waveform via the capillary array circuit board.

19. The multiplex capillary electrophoresis system of claim 18 , further comprising an electrode array communicating with the capillary array circuit board, wherein the pulse-field alternating current power supply is configured to apply the first pulse-field waveform and the second pulse-field waveform further via the electrode array.

20. The multiplex capillary electrophoresis system of claim 19 , wherein the capillaries comprise respective capillary tips, and the electrode array comprises electrodes disposed adjacent to the respective capillary tips.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 30, 2019
From: ADVANCED ANALYTICAL TECHNOLOGIES, INC.
To: AGILENT TECHNOLOGIES, INC.
Reel/Frame 049317/0593 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 28, 2017
From: VER MEER, MARK R.; UTHE, JOLITA J.; WEI, WEI; FOSTER, MARTIN CHRIS; BOEKE, BRUCE R.
To: ADVANCED ANALYTICAL TECHNOLOGIES, INC.
Reel/Frame 043688/0545 →
Continuity (7)
Continuation In Part 14984039 · Dec 30, 2015
Continuation In Part 14983985 · Dec 30, 2015
Continuation In Part 14822956 · Aug 11, 2015
Continuation 13470870 · May 14, 2012
Continuation In Part 29421549 · Mar 15, 2012
Provisional Application 61643411 · May 7, 2012
Related Publication 20180038827A1 · Feb 8, 2018
Cited By (1)
US 12,366,551