Use of polysaccharides to control protein adsorption to the air–water interface

2006 ◽  
Vol 20 (6) ◽  
pp. 872-878 ◽  
Author(s):  
Renate A. Ganzevles ◽  
Martien A. Cohen Stuart ◽  
Ton van Vliet ◽  
Harmen H.J. de Jongh
2006 ◽  
Vol 398 (3) ◽  
pp. 569-576 ◽  
Author(s):  
Silvia Belem-Gonçalves ◽  
Pascale Tsan ◽  
Jean-Marc Lancelin ◽  
Tito L. M. Alves ◽  
Vera M. Salim ◽  
...  

The interfacial properties of bovine testicular hyaluronidase were investigated by demonstrating the association of hyaluronidase activity with membranes prepared from bovine testis. Protein adsorption to the air/water interface was investigated using surface pressure-area isotherms. In whichever way the interfacial films were obtained (protein injection or deposition), the hyaluronidase exhibited a significant affinity for the air/water interface. The isotherm obtained 180 min after protein injection into a pH 5.3 subphase was similar to the isotherm obtained after spreading the same amount of protein onto the same subphase, indicating that bovine testicular hyaluronidase molecules adopted a similar arrangement and/or conformation at the interface. Increasing the subphase pH from 5.3 to 8 resulted in changes of the protein isotherms. These modifications, which could correspond to the small pH-induced conformational changes observed by Fourier-transform IR spectroscopy, were discussed in relation to the pH influence on the hyaluronidase activity. Adding hyaluronic acid, the enzyme substrate, to the subphase tested the stability of the interfacial properties of hyaluronidase. The presence of hyaluronic acid in the subphase did not modify the protein adsorption and allowed substrate binding to a preformed film of hyaluronidase at pH 5.3, the optimal pH for the enzyme activity. Such effects of hyaluronic acid were not observed when the subphase was constituted of pure water, a medium where the enzyme activity was negligible. These influences of hyaluronic acid were discussed in relation to the modelled structure of bovine testis hyaluronidase where a hydrophobic region was proposed to be opposite of the catalytic site.


2009 ◽  
Vol 23 (1) ◽  
pp. 221-224 ◽  
Author(s):  
Dmitry O. Grigoriev ◽  
Eric Kolodziejczyk ◽  
Martin E. Leser ◽  
Martin Michel ◽  
Reinhard Miller

Langmuir ◽  
2019 ◽  
Vol 35 (49) ◽  
pp. 16087-16100
Author(s):  
Paola Brocca ◽  
Andrea Saponaro ◽  
Bianca Introini ◽  
Valeria Rondelli ◽  
Martina Pannuzzo ◽  
...  

Langmuir ◽  
2016 ◽  
Vol 32 (38) ◽  
pp. 9892-9898 ◽  
Author(s):  
Yohko F. Yano ◽  
Yuki Kobayashi ◽  
Toshiaki Ina ◽  
Kiyofumi Nitta ◽  
Tomoya Uruga

Langmuir ◽  
2012 ◽  
Vol 28 (20) ◽  
pp. 7780-7787 ◽  
Author(s):  
Kathrin Engelhardt ◽  
Armin Rumpel ◽  
Johannes Walter ◽  
Jannika Dombrowski ◽  
Ulrich Kulozik ◽  
...  

Author(s):  
Randall W. Smith ◽  
John Dash

The structure of the air-water interface forms a boundary layer that involves biological ,chemical geological and physical processes in its formation. Freshwater and sea surface microlayers form at the air-water interface and include a diverse assemblage of organic matter, detritus, microorganisms, plankton and heavy metals. The sampling of microlayers and the examination of components is presently a significant area of study because of the input of anthropogenic materials and their accumulation at the air-water interface. The neustonic organisms present in this environment may be sensitive to the toxic components of these inputs. Hardy reports that over 20 different methods have been developed for sampling of microlayers, primarily for bulk chemical analysis. We report here the examination of microlayer films for the documentation of structure and composition.Baier and Gucinski reported the use of Langmuir-Blogett films obtained on germanium prisms for infrared spectroscopic analysis (IR-ATR) of components. The sampling of microlayers has been done by collecting fi1ms on glass plates and teflon drums, We found that microlayers could be collected on 11 mm glass cover slips by pulling a Langmuir-Blogett film from a surface microlayer. Comparative collections were made on methylcel1ulose filter pads. The films could be air-dried or preserved in Lugol's Iodine Several slicks or surface films were sampled in September, 1987 in Chesapeake Bay, Maryland and in August, 1988 in Sequim Bay, Washington, For glass coverslips the films were air-dried, mounted on SEM pegs, ringed with colloidal silver, and sputter coated with Au-Pd, The Langmuir-Blogett film technique maintained the structure of the microlayer intact for examination, SEM observation and EDS analysis were then used to determine organisms and relative concentrations of heavy metals, using a Link AN 10000 EDS system with an ISI SS40 SEM unit. Typical heavy microlayer films are shown in Figure 3.


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