THE AFFINITY TECHNOLOGY IN DOWNSTREAM PROCESSING

被引:89
作者
LABROU, N [1 ]
CLONIS, YD [1 ]
机构
[1] AGR UNIV ATHENS,DEPT AGR BIOL & BIOTECHNOL,TECHNOL ENZYMAT LAB,GR-11855 ATHENS,GREECE
关键词
DOWNSTREAM PROCESSING; BIOSEPARATION; ENZYME PURIFICATION; BIOCATALYST PURIFICATION; AFFINITY TECHNOLOGY; AFFINITY CHROMATOGRAPHY; AFFINITY LIGAND; AFFINITY ADSORBENT; DYE LIGAND;
D O I
10.1016/0168-1656(94)90047-7
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The quality criteria imposed on several biochemicals are stringent, thus, high-separation purification technology is important to downstream processing. Affinity-based purification technologies are regarded as the finest available, and each one differs in its purifying ability, economy, processing speed and capacity. The most widely used affinity technology is classical affinity chromatography, however, other chromatography-based approaches have also been developed, for example, perfusion affinity chromatography, hyperdiffusionTM affinity chromatography, high-perfor mance affinity chromatography, centrifugal affinity chromatography, affinity repulsion chromatography, heterobifunctional ligand affinity chromatography and the various chromatographic applications of 'affinity tails'. On the other hand, non-chromatographic affinity technologies aim at high throughput and seek to circumvent problems associated with diffusion limitations experienced with most chromatographic packings. Continuous affinity recycle extraction, aqueous two-phase affinity partitioning, membrane affinity filtration, affinity cross-flow ultrafiltration, reversible soluble affinity polymer separation and affinity precipitation are all non-chromatographic technologies. Several types of affinity ligands are used to different extents; antibodies and their fragments, receptors and their binding substances, avidin/biotin systems, textile and biomimetic dyes, (oligo)peptides, antisense peptides, cheIated metal cations, lectins and phenylboronates, protein A and G, calmodulin, DNA, sequence-specific DNA, (oligo)nudeotides and heparin. Likewise, there are several support types developed and used; natural, synthetic, inorganic and composite materials.
引用
收藏
页码:95 / 119
页数:25
相关论文
共 158 条
[51]  
Dean P.D.G., 1985, AFFINITY CHROMATOGRA
[52]   PARTIAL-PURIFICATION OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE AND PHOSPHOFRUCTOKINASE FROM RAT ERYTHROCYTE HEMOLYSATE BY PARTITIONING IN AQUEOUS 2-PHASE SYSTEMS [J].
DELGADO, C ;
TEJEDOR, MC ;
LUQUE, J .
JOURNAL OF CHROMATOGRAPHY, 1990, 498 (01) :159-168
[53]   LIGAND RECEPTOR INTERACTIONS IN AFFINITY CELL PARTITIONING - STUDIES WITH TRANSFERRIN COVALENTLY LINKED TO MONOMETHOXYPOLY(ETHYLENE GLYCOL) AND RAT RETICULOCYTES [J].
DELGADO, C ;
SANCHO, P ;
MENDIETA, J ;
LUQUE, J .
JOURNAL OF CHROMATOGRAPHY, 1992, 594 (1-2) :97-103
[54]   PROTEIN-PURIFICATION USING COMBINED STREPTAVIDIN (OR AVIDIN)-SEPHAROSE AND THIOPROPYL-SEPHAROSE AFFINITY-CHROMATOGRAPHY [J].
DESARNAUD, F ;
MARIE, J ;
LARGUIER, R ;
LOMBARD, C ;
JARD, S ;
BONNAFOUS, JC .
JOURNAL OF CHROMATOGRAPHY, 1992, 603 (1-2) :95-104
[55]   IDENTIFICATION, PURIFICATION AND RECONSTITUTION OF THIAMIN METABOLIZING ENZYMES IN HUMAN RED-BLOOD-CELLS [J].
EGI, Y ;
KOYAMA, SY ;
SHIODA, T ;
YAMADA, K ;
KAWASAKI, T .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1160 (02) :171-178
[56]  
EHLE H, 1990, BIOSEPARATIONS, V3, P47
[57]  
ELKAK A, 1990, BIOSEPARATION, V3, P47
[58]   SILICA SORBENTS WITH ONE-SITE AND 2-SITE ATTACHED BACITRACIN IN AFFINITY-CHROMATOGRAPHY [J].
FADEEV, AY ;
MINGALYOV, PG ;
STAROVEROV, SM ;
LUNINA, EV ;
LISICHKIN, GV ;
GAIDA, AV ;
MONASTYRSKY, VA .
JOURNAL OF CHROMATOGRAPHY, 1992, 596 (01) :114-117
[59]   SELECTIVE PURIFICATION OF MICROTUBULE-ASSOCIATED PROTEIN-1 AND PROTEIN-2 FROM RAT-BRAIN USING POLY(L-ASPARTIC ACID) [J].
FUJII, T ;
NAKAMURA, A ;
OGOMA, Y ;
KONDO, Y ;
ARAI, T .
ANALYTICAL BIOCHEMISTRY, 1990, 184 (02) :268-273
[60]  
GALAEV IY, 1993, 6TH EUR C BIOT FLOR, V1