Métodos de Separación de Proteinas

Proteínas: métodos de estudio
Eliécer Jiménez Charris

Eliecer.jimenez@correounivalle.edu.co
Proteínas
• Son componentes abundantes en todas las
células.
• Casi todas son importantes para las funciones

biológicas y/o la estructura celular.
Métodos de homogenización
Mecánicos Sonicador
Homogenizador
Perlas de
vidrio
Químicos / Térmicos Lisis por Detergentes
Lisis por
lisozima
Nitrógeno liquido
Radio del tubo (r)
Masa (m)
Volúmen de la partícula (V) (Vp)
Velocidad angular (w- rad.s-1)
Densidad de la solución (p)

SEPARACIÓN DE LAS PROTEÍNAS
POR ELECTROFORESIS
SEPARACIÓN DE LAS PROTEÍNAS
POR CROMATOGRAFÍA
Tipos de cromatografía
Basics of Chromatography
Jony Mallik
Introductory Principles
Chromatography is a combination of two words;
* Chromo – Meaning color
* Graphy – representation of something on paper
History of Chromatography
Chromatography, literally "color writing", was first employed by Russian

scientist Mikhail Tswett in 1903/1906. He continued to work with
chromatography in the first decade of the 20th century, primarily for the
separation of plant pigments such as chlorophyll, carotenes, and xanthophylls.
Since these components have different colors (green, orange, and
yellow,respectively) they gave the technique its name.
It is a physical separation method of separation in which
the components of a mixture are separated by differences in
their distribution between two phases, one of which is
stationary (stationary phase) while the other (mobile
phase) moves through it in a definite direction. The
substances must interact with the stationary phase to be
retained and separated by it.
Definition of chromatography
IUPAC definition (International Union of pure and applied

Chemistry) (1993):
Chromatography is a physical method of separation in which the
components to be separated are distributed between two phases,
one of which is stationary while the other moves in a definite
direction.
The stationary phase may be a solid, or a liquid supported on a

solid or gel, the mobile phase may be either a gas or a liquid.
CHROMATOGRAPHY
 Analyze
Separate • Identify
• Purify
• Quantify
Mixture Components
 Chromatograph: Instrument employed for a chromatography.
 Eluent: Fluid entering a column.
 Eluate: Fluid exiting the column.
 Elution: The process of passing the mobile phase through the column.
 Flow rate: How much mobile phase passed / minute (ml/min).
 Linear velocity: Distance passed by mobile phase per 1 min in the

column (cm/min).
Mobile Phase – gas or liquid that carries the mixture of
components through the stationary phase.
Stationary Phase – the part of the apparatus that holds
the components as they move through it,
separating them.
Uses for Chromatography
Chromatography is used by scientists to:
•Analyze – examine a mixture, its components, and their
relations to one another
•Identify – determine the identity of a mixture or
components based on known components
•Purify – separate components in order to isolate one of
interest for further study
•Quantify – determine the amount of the a mixture
and/or the components present in the sample
Real-life examples of uses for chromatography:
Pharmaceutical Company
Hospital
Law Enforcement
Environmental Agency
Manufacturing Plant
Chromatogram:
It is the visual output of the chromatograph.
Chromatograph:
It is equipment that enables a sophisticated Separation.
Stationary phase (bounded phase):

It is a phase that is covalently bonded to the support particles or to the
inside wall of the column tubing.
Mobile phase:
It is the phase which moves in a definite direction.
Analyte (Sample):
It is the substance to be separated during chromatography.
Eluate:
It is the mobile phase leaving the column.
Retention time:
It is the characteristic time it takes for a particular analyte to pass
through the system (from the column inlet to the detector) under set
conditions.
Eluent:
It is the solvent that will carry the analyte.
Retardation factor (R):
Fraction of an analyte in the mobile phase of a chromatographic
system.
•Liquid Chromatography – separates liquid samples with a liquid solvent
(mobile phase) and a column composed of solid beads (stationary phase)
• Gas Chromatography – separates vaporized samples with a carrier gas

(mobile phase) and a column composed of a liquid or of solid beads
(stationary phase)
•Paper Chromatography – separates dried liquid samples with a liquid

solvent (mobile phase) and a paper strip (stationary phase)
•Thin-Layer Chromatography – separates dried liquid samples with a

liquid solvent (mobile phase) and a glass plate covered with a thin layer of
alumina or silica gel (stationary phase)
GEL FILTRATION
 Gel filtration separates molecules according to the differences

in size as they pass through the filtration medium packed in
the column.
 It is well suited for biomolecules that are sensitive to pH
,concentration and harsh environment.
 Parameters that affects gel filtration are, particle size, flow
rate, packaging density, porosity of the particle and viscosity
of the mobile phase.
MATERIALS REQUIRED
 Cross linked dextrans (sephadex)

 Agarose (sepharose)
 Polyacrylamide
 Porous glass gel.
APPLICATIONS
 Fractionation (purification of the desired protein using suitable gel)
 Molecular weight determination
ION EXCHANGE
Ion exchange
chromatography is used to
remove ions of one type
from a mixture and replace
them by ions of another
type.
The basic principle is
reversible competitive
binding
ION EXCHANGERS
• Cation exchangers (negative ions – stationary)
• Anion exchangers (positive ions - stationary)
Four types of polymers are commonly used. They are,
• Synthetic hydrophobic polymer resins crosslinked with
divinylbenzene.
• Naturally occuring as well as synthetic polymers(cellulose)
• Synthetic hydrophilic polymers
• Silica gel
AFFINITY CHROMATOGRAPHY
• Affinity chromatography includes

bioaffinity, dye-ligand affinity
and immobilized metal ion
afffinity techniques.
• It is based on the formation of
the specific and reversible
complexes between a pair of
biomolecules.
HPLC
HPLC is a physical separation technique in which a sample

dissolved in a liquid is injected into a column packed with
small particles and it is separated into its constituent
components
HPLC is probably the most important and widely used
analytical technique for quantitative analysis of organics and
biomolecules
HPLC is applicable to many kind of samples:
Most useful for pharmaceuticals, biomolecules, and labile
organics
HPLC Instrumentation Overview
Principle Pattern An Example
Solvent Reservoirs
Controller
Solvent Cabinet Vacuum Degasser
Binary Pump
Autosampler
Thermostatted
Column Compartment
Detector
37

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Proteínas: métodos de estudio

Eliécer Jiménez Charris

• Casi todas son importantes para las funciones

Volúmen de la partícula (V) (Vp)

Velocidad angular (w- rad.s-1)

Densidad de la solución (p)

Chromatography, literally "color writing", was first employed by Russian

IUPAC definition (International Union of pure and applied

The stationary phase may be a solid, or a liquid supported on a

 Eluent: Fluid entering a column.

 Eluate: Fluid exiting the column.

 Flow rate: How much mobile phase passed / minute (ml/min).

 Linear velocity: Distance passed by mobile phase per 1 min in the

Stationary phase (bounded phase):

• Gas Chromatography – separates vaporized samples with a carrier gas

•Paper Chromatography – separates dried liquid samples with a liquid

•Thin-Layer Chromatography – separates dried liquid samples with a

 Gel filtration separates molecules according to the differences

 Cross linked dextrans (sephadex)

• Affinity chromatography includes

HPLC is a physical separation technique in which a sample

Solvent Cabinet Vacuum Degasser

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