Supramolecular chemistry of cyclodextrins in enzyme technology

被引:336
作者
Villalonga, Reynaldo
Cao, Roberto [1 ]
Fragoso, Alex
机构
[1] Univ Havana, Lab Bioinorgan Chem, Fac Chem, Havana 10400, Cuba
[2] Univ Matanzas, Ctr Enzyme Technol, Matanzas 44740, Cuba
[3] Univ Rovira & Virgili, Nanobiotechnol & Bioanal Grp, Dept Chem Engn, Tarragona 43007, Spain
关键词
D O I
10.1021/cr050253g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cyclodextrins (CDs) and their derivatives has been used in a range of applications related to enzymes specifically in the preparation of biosensors. The dynamic nature of host-guest interactions between CD derivatives and enzymes is exploited to increase the sensitivity of biosensing devices through signal amplification. Similarly, recycling of modified surfaces is also possible in devices containing complementary pairs of host/guest molecules due the reversible nature of the supramolecular interactions. Consequently, the use of molecular imprinting technology in CD-containing polymers should lead to improved results. One approach consists of formation of self-assembled monolayers of CDs using microcontact printing or nanoprint lithography. Currently, nanodevices for use as smart carriers is being developed that is able to target cells. In this sense, polymeric CD-containing nanocapsules with photoactive metal complexes included in the cavities can be used or the use of CdSe or CdS quantum dots capped with CDs which are able to supramolecularly associate drugs and target biomolecules while the semiconductor emits its intense fluorescent signal. The CD-enzyme interactions will also benefit biotechnological processes specifically downstream processes favoring easy recovery of valuable proteins produced by fermentation and cell culture technology.
引用
收藏
页码:3088 / 3116
页数:29
相关论文
共 321 条
  • [1] AESCHLIMANN D, 1994, THROMB HAEMOSTASIS, V71, P402
  • [2] Molecular chaperone-like activity of hydrogel nanoparticles of hydrophobized pullulan: Thermal stabilization with refolding of carbonic anhydrase B
    Akiyoshi, K
    Sasaki, Y
    Sunamoto, J
    [J]. BIOCONJUGATE CHEMISTRY, 1999, 10 (03) : 321 - 324
  • [3] Akkara J. A., 2000, U.S. Patent, Patent No. [6063916, 6,063,916]
  • [4] A CONVENIENT SYNTHESIS OF 7-ALPHA-HYDROXYCHOLEST-4-EN-3-ONE BY THE HYDROXYPROPYL-BETA-CYCLODEXTRIN-FACILITATED CHOLESTEROL OXIDASE OXIDATION OF 3-BETA,7-ALPHA-CHOLEST-5-ENE-3,7-DIOL
    ALEXANDER, DL
    FISHER, JF
    [J]. STEROIDS, 1995, 60 (03) : 290 - 294
  • [5] Water-soluble platinum and palladium nanoparticles modified with thiolated β-cyclodextrin
    Alvarez, J
    Liu, J
    Román, E
    Kaifer, AE
    [J]. CHEMICAL COMMUNICATIONS, 2000, (13) : 1151 - 1152
  • [6] Dendrimeric micelles for controlled drug release and targeted delivery
    Ambade, Ashootosh V.
    Savariar, Elamprakash N.
    Thayumanavan, S.
    [J]. MOLECULAR PHARMACEUTICS, 2005, 2 (04) : 264 - 272
  • [7] AMSTRONG FA, 2000, ELECTROCHIM ACTA, V45, P2623
  • [8] Persubstituted cyclodextrin-based glycoclusters as inhibitors of protein-carbohydrate recognition using purified plant and mammalian lectins and wild-type and lectin-gene-transfected tumor cells as targets
    André, S
    Kaltner, H
    Furuike, T
    Nishimura, SI
    Gabius, HJ
    [J]. BIOCONJUGATE CHEMISTRY, 2004, 15 (01) : 87 - 98
  • [9] [Anonymous], 1996, CYCLODEXTRINS, DOI [DOI 10.1016/B978-0-12-804307-3.00004-1, DOI 10.13140/RG.2.2.35859.68642]
  • [10] Growth of gold nanoparticles in human cells
    Anshup
    Venkataraman, JS
    Subramaniam, C
    Kumar, RR
    Priya, S
    Kumar, TRS
    Omkumar, RV
    John, A
    Pradeep, T
    [J]. LANGMUIR, 2005, 21 (25) : 11562 - 11567