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Dive into the research topics where Susanne Wikman is active.

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Featured researches published by Susanne Wikman.


Biosensors and Bioelectronics | 2009

Theoretical and computational strategies for rational molecularly imprinted polymer design

Ian A. Nicholls; Håkan S. Andersson; Christy Charlton; Henning Henschel; Björn C. G. Karlsson; Jesper G Karlsson; John O'Mahony; Annika M. Rosengren; Susanne Wikman

The further evolution of molecularly imprinted polymer science and technology necessitates the development of robust predictive tools capable of handling the complexity of molecular imprinting systems. A combination of the rapid growth in computer power over the past decade and significant software developments have opened new possibilities for simulating aspects of the complex molecular imprinting process. We present here a survey of the current status of the use of in silico-based approaches to aspects of molecular imprinting. Finally, we highlight areas where ongoing and future efforts should yield information critical to our understanding of the underlying mechanisms sufficient to permit the rational design of molecularly imprinted polymers.


Analytica Chimica Acta | 2001

Can we rationally design molecularly imprinted polymers

Ian A. Nicholls; Karina Adbo; Håkan S. Andersson; Per Ola Andersson; Jonas Ankarloo; Jimmy Hedin-Dahlström; Päivi Jokela; Jesper G Karlsson; Linus Olofsson; Jenny P. Rosengren; Siamak Shoravi; Johan Svenson; Susanne Wikman

The nearly exponential growth in the molecular imprinting literature has to a large extent been fuelled by an increasing awareness of the potential of molecular imprinting based technologies. Despite the acceptance of the technique by cognate disciplines and the demonstration of its usefulness in a number of enabling technologies, relatively little is known about the molecular level events underlying the imprinting process and subsequent recognition events. What rules govern imprint formation? Can we use such rules to rationally design molecularly imprinted polymers?


Analytical and Bioanalytical Chemistry | 2011

Rational design of biomimetic molecularly imprinted materials: theoretical and computational strategies for guiding nanoscale structured polymer development

Ian A. Nicholls; Håkan S. Andersson; Kerstin Golker; Henning Henschel; Björn C. G. Karlsson; Gustaf D. Olsson; Annika M. Rosengren; Siamak Shoravi; Subramanian Suriyanarayanan; Jesper G. Wiklander; Susanne Wikman

In principle, molecularly imprinted polymer science and technology provides a means for ready access to nano-structured polymeric materials of predetermined selectivity. The versatility of the technique has brought it to the attention of many working with the development of nanomaterials with biological or biomimetic properties for use as therapeutics or in medical devices. Nonetheless, the further evolution of the field necessitates the development of robust predictive tools capable of handling the complexity of molecular imprinting systems. The rapid growth in computer power and software over the past decade has opened new possibilities for simulating aspects of the complex molecular imprinting process. We present here a survey of the current status of the use of in silico-based approaches to aspects of molecular imprinting. Finally, we highlight areas where ongoing and future efforts should yield information critical to our understanding of the underlying mechanisms sufficient to permit the rational design of molecularly imprinted polymers.


Organic and Biomolecular Chemistry | 2005

TBADH activity in water-miscible organic solvents: correlations between enzyme performance, enantioselectivity and protein structure through spectroscopic studies

Linus Olofsson; Ian A. Nicholls; Susanne Wikman

The enantioselective reduction of 2-pentanone to (R)- and (S)-2-pentanol by Thermoanaerobacter (formerly Thermoanaerobium) brockii alcohol dehydrogenase (TBADH) in mixtures of water and water-miscible organic solvents was investigated. Significant enzymatic activity was retained in up to 87% methanol, ethanol and acetonitrile. The changes in enzyme activity as a function of organic solvent were correlated to structural alterations of TBADH with a series of spectroscopic studies (fluorescence, fluorescence quenching and circular dichroism (CD)). Interestingly, this study shows that the tetrameric form of TBADH is not critical for catalytic performance.


International Journal of Molecular Sciences | 2010

Escherichia coli mar and acrAB Mutants Display No Tolerance to Simple Alcohols

Jonas Ankarloo; Susanne Wikman; Ian A. Nicholls

The inducible Mar phenotype of Escherichia coli is associated with increased tolerance to multiple hydrophobic antibiotics as well as some highly hydrophobic organic solvents such as cyclohexane, mediated mainly through the AcrAB/TolC efflux system. The influence of water miscible alcohols ethanol and 1-propanol on a Mar constitutive mutant and a mar deletion mutant of E. coli K-12, as well as the corresponding strains carrying the additional acrAB deletion, was investigated. In contrast to hydrophobic solvents, all strains were killed in exponential phase by 1-propanol and ethanol at rates comparable to the parent strain. Thus, the Mar phenotype does not protect E. coli from killing by these more polar solvents. Surprisingly, AcrAB does not contribute to an increased alcohol tolerance. In addition, sodium salicylate, at concentrations known to induce the mar operon, was unable to increase 1-propanol or ethanol tolerance. Rather, the toxicity of both solvents was increased in the presence of sodium salicylate. Collectively, the results imply that the resilience of E. coli to water miscible alcohols, in contrast to more hydrophobic solvents, does not depend upon the AcrAB/TolC efflux system, and suggests a lower limit for substrate molecular size and functionality. Implications for the application of microbiological systems in environments containing high contents of water miscible organic solvents, e.g., phage display screening, are discussed.


Nordic Studies in Science Education | 2015

University students' reflections on representations in genetics and stereochemistry revealed by a focus group approach

Inger Edfors; Susanne Wikman; Brita Johansson Cederblad; Cedric Linder

Genetics and organic chemistry are areas of science that students regard as difficult to learn. Part of this difficulty is derived from the disciplines having representations as part of their discourses. In order to optimally support students’ meaning-making, teachers need to use representations to structure the meaning-making experience in thoughtful ways that consider the variation in students’ prior knowledge. Using a focus group setting, we explored 43 university students’ reasoning on representations in introductory chemistry and genetics courses. Our analysis of eight focus group discussions revealed how students can construct somewhat bewildered relations with disciplinary-specific representations. The students stated that they preferred familiar representations, but without asserting the meaning-making affordances of those representations. Also, the students were highly aware of the affordances of certain representations, but nonetheless chose not to use those representations in their problem solving. We suggest that an effective representation is one that, to some degree, is familiar to the students, but at the same time is challenging and not too closely related to “the usual one”. The focus group discussions led the students to become more aware of their own and others ways of interpreting different representations. Furthermore, feedback from the students’ focus group discussions enhanced the teachers’ awareness of the students’ prior knowledge and limitations in students’ representational literacy. Consequently, we posit that a focus group setting can be used in a university context to promote both student meaning-making and teacher professional development in a fruitful way.


Journal of Organic Chemistry | 2006

A class II aldolase mimic

Jimmy Hedin-Dahlström; Jenny Rosengren-Holmberg; Sacha Legrand; Susanne Wikman; Ian A. Nicholls


Journal of Molecular Catalysis B-enzymatic | 2011

Effect of the cross-linker on the general performance and temperature dependent behaviour of a molecularly imprinted polymer catalyst of a Diels–Alder reaction

Henning Henschel; Nicole Kirsch; Jimmy Hedin-Dahlström; Michael J. Whitcombe; Susanne Wikman; Ian A. Nicholls


Tetrahedron-asymmetry | 2004

Stereoselective reduction of menthone by molecularly imprinted polymers

Jimmy Hedin-Dahlström; Siamak Shoravi; Susanne Wikman; Ian A. Nicholls


Archive | 2013

Rational molecularly imprinted polymer design : theoretical and computational strategies

Ian A. Nicholls; Håkan S. Andersson; Kerstin Golker; Henning Henschel; Björn C. G. Karlsson; Gustaf D. Olsson; Annika M. Rosengren; Siamak Shoravi; Jesper G. Wiklander; Susanne Wikman

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