Literature DB >> 540124

Structural investigation of biological material in aqueous environment by means of infrared-ATR spectroscopy.

P Hofer, U P Fringeli.   

Abstract

Infrared attenuated total reflection (ATR) spectroscopy may be used to investigate biological material (e.g., membranes, proteins, erythrocytes etc.) under biological conditions provided that adhesion of the sample can be achieved in aqueous environment. Uncharged lipid multilayer model membranes can be attached by hydrophobic interaction when hydrophobic internal reflection plates (e.g., ZnSe, CdTe) are used. However, if an electric field is applied across the membrane, germanium reflection elements would be preferred because of their low electric resistance (approximately 50 omega cm). This material can also be used if cells or proteins are linked chemically to the ATR plate because of the hydrophilic surface which is similar to that of glass and, thus, enables chemical modification by silanization. It has turned out that good adhesion of uncharged and negatively charged model membranes to germanium plates is achieved when they are coated with a monomolecular layer of aminopropylsilane. There is some evidence that erythrocytes remain more stable when adsorbed to a polymerized aminosilane coating (organic silanization) rather than to the corresponding monolayer (aqueous silanization). Negatively charged germanium surfaces have been obtained by succinylation of the aminosilane coating. Furthermore it has been demonstrated that proteins can be bound to the aminosilane coating by means of carbodiimide. Immobilized acetylcholinesterase was still enzymatically active.

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Year:  1979        PMID: 540124     DOI: 10.1007/BF00537596

Source DB:  PubMed          Journal:  Biophys Struct Mech        ISSN: 0340-1057


  11 in total

1.  Covalent coupling methods for inorganic support materials.

Authors:  H H Weetall
Journal:  Methods Enzymol       Date:  1976       Impact factor: 1.600

2.  Stability, inhibition and reactivation of acetylcholinesterase covalently coupled to glass.

Authors:  G Baum; F B Ward; H H Weetall
Journal:  Biochim Biophys Acta       Date:  1972-05-12

3.  Molecular properties of acetylcholinesterase.

Authors:  W Leuzinger; M Goldberg; E Cauvin
Journal:  J Mol Biol       Date:  1969-03-14       Impact factor: 5.469

4.  Storage stability of water-insoluble enzymes convalently coupled to organic and inorganic carriers.

Authors:  H H Weetall
Journal:  Biochim Biophys Acta       Date:  1970-07-15

5.  Alkaline phosphatase insolubilized by covalent linkage to porous glass.

Authors:  H H Weetall
Journal:  Nature       Date:  1969-08-30       Impact factor: 49.962

6.  Trypsin and papain covalently coupled to porous glass: preparation and characterization.

Authors:  H H Weetall
Journal:  Science       Date:  1969-10-31       Impact factor: 47.728

7.  Coupling polylysine to glass beads for plasma membrane isolation.

Authors:  B S Jacobson; J Cronin; D Branton
Journal:  Biochim Biophys Acta       Date:  1978-01-04

8.  Porous glass as a solid support for immobilisation or affinity chromatography of enzymes.

Authors:  P J Robinson; P Dunnill; M D Lilly
Journal:  Biochim Biophys Acta       Date:  1971-09-22

9.  Instability of Langmuir-Blodgett layers of barium stearate, cadmium arachidate and tripalmitin, studied by means of electron microscopy and infrared spectroscopy.

Authors:  F Kopp; U P Fringeli; K Mühlethaler; H H Günthard
Journal:  Biophys Struct Mech       Date:  1975-02-19

10.  The structure of lipids and proteins studied by attenuated total reflection (ATR) infrared spectroscopy. II. Oriented layers of a homologous series: phosphatidylethanolamine to phosphatidylcholine.

Authors:  U P Fringeli
Journal:  Z Naturforsch C Biosci       Date:  1977 Jan-Feb
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  2 in total

1.  Structure-activity relationship in vinculin: an IR/attenuated total reflection spectroscopic and film balance study.

Authors:  U P Fringeli; P Leutert; H Thurnhofer; M Fringeli; M M Burger
Journal:  Proc Natl Acad Sci U S A       Date:  1986-03       Impact factor: 11.205

2.  Secondary structure and Pd(II) coordination in S-layer proteins from Bacillus sphaericus studied by infrared and X-ray absorption spectroscopy.

Authors:  Karim Fahmy; Mohamed Merroun; Katrin Pollmann; Johannes Raff; Olesya Savchuk; Christoph Hennig; Sonja Selenska-Pobell
Journal:  Biophys J       Date:  2006-05-12       Impact factor: 4.033

  2 in total

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