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Capillary Electrophoresis with Glycerol as an Additive

2025-05-09 生物化学 加入收藏
Two kinds of semi-liquid separation media are frequently used for the separation

Two kinds of semi-liquid separation media are frequently used for the separation of DNA by high performance capillary electrophoresis (CE), namely dynamic or entangled free solution polymer sieving matrix, and dilute liquid-gel solutions. Polymer solutions may be defined in three different functional concentrations: dilute, semidilute, and entangled. In dilute solutions, the polymer molecules are physically separate; as the concentration of polymer increases the molecules begin to interact, and at a critical concentration the polymers begin to physically interact to form an entangled physical network (1 –3 ). These media have the ability to act as size selective sieving agents that partition DNA molecules, but since the media are liquid the injection of fresh media and the removal of expended media are facilitated. The media are typically neutral high molecular weight polymers and polymer sugars, which provide a high uniformity of electrophoretic medium if capillary electroosmotic flow (EOF) effects are suppressed. For the purpose of this review, particular attention will be drawn to entangled free solution capillary electrophoresis (ESCE) using Tris-borate-EDTA (TBE) buffers, with glycerol as an additive. For DNA separations, many different ESCE sieving media and dilute liquid-gel solutions have been used (Table 1 ): polysaccharide polymers such as, hydroxypropyl cellulose (HPC) (2 –4 ), hydroxypropyl methyl cellulose (HPMC) (5 –7 ), methyl cellulose (8 ,9 ), hydroxyethyl cellulose (HEC) (3 ,7 ,10 –15 ), dextran (16 ,17 ), TreviSol (18 ), semi-liquid agarose (19 ,20 ), and galactomannans (1 ). Nonsaccharide polymers such as linear polyacrylamides and substituted polyacrylamides (3 ,7 ,10 –26 ), linear and branched poly(ethylene oxides), and poly vinyl polymers (27 ) are also employed for a wide variety of separations purposes. Table 1  Application of Glycerol Containing Buffers for DNA Analysis by CE a

Assay

Matrix

Buffer

Detector

Comment

Ref.

dsDNA PCR-RFLP

HPMC

TBE/glycerol�ethidium

UV, LIF

Glycerol improves resolution

5,6,46,47,49

dsDNA PCR-RFLP

0.2–1% HEC

TBE

UV

Good resolution

2,4,10,11

STR-PCR PCR-RFLP

0.5% MC

0.5–2.5X TBE TAE

YoPro, LIF, no dye, UV

Better resolution in TBE

8,9,15

STR-PCR PCR-RFLP

1.25% HEC

TBE 7 M urea

no dye, UV

Good resolution of several STR

14

Supercoil plasmid

0.1–0.3% HEC

0.5–2.5X TBE

UV

Good resolution

54

dsDNA LCR

HPMC

TBE/glycerol

LIF

Good resolution 25 and 50 bp

48

dsDNA PCR-RFLP

0.5% PEO

TBE/dyes

LIF

Good resolution

27,55

dsDNA PCR-RFLP

Liquid

TBE


Better resolution in TBE

20,39


Aragose

TAE




dsDNA PCR-RFLP

Trevisol

TAPS

UV

Good resolution

18

HPA

HPMC

TBE/glycerol�ethidium

UV, LIF

Glycerol improves resolution

50

SSCP

HPMC

TBE/glycerol�ethidium

UV. LIF

Glycerol stablizes confomers

51

SSCP

LPA

TBE�glycerol

UV

Good resolution

17,22,52,57

dsDNA PCR-RFLP

LPA

TBE�ethidium

UV

Good resolution

21,24,44

RNA

HPMC

TBE 7 M urea

UV

Glycerol diminishes resolution

45

a Some comments on the effects of glycerol and borate on DNA resolution are noted.


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