Abstract

Anticancer peptides (ACPs) are polycationic amphiphiles capable of preferentially killing a widespectrum of cancer cells relative to non-cancerous cells. Their primary mode of action is aninteraction with the cell membrane and subsequent activation of lytic effects, however it remainscontroversial the exact mechanism responsible for this mode of action. It has in previous studies been shown that utilizing zeta potential analyses it was possible to demonstrate the interaction of a small anticancer peptide with membrane modelsystems and cancer cells. Electrostatic interactions have a pivotal role in the cell killing processand in contrast to the AMPs action cell death occurs without achieving full neutralization of themembrane charge. The advent of microarray technology has revolutionized the search for genes that are differentially expressed across a range of cell types or experimental conditions. Traditional clustering methods, such as hierarchical clustering, are often difficult to deploy effectively since genes rarely exhibit similar expression pattern across a wide range of conditions. Web-enabled service called GEMS (Gene Expression Mining Server) for biclustering microarray data where Users may upload expression data and specify a set of criteria.GEMS performs bicluster mining based on a Gibbs sampling paradigm. Here, in Biogenea we have for the first time discovered an Anticancer Peptide SVS-1 multipharmacophore with an ini silico evaluated Efficacy in Preceding Membrane Neutralization using a web server for biclustering analysis of expression data. Quantum information processing devices need to be robust and stable against external noise and internal imperfections to ensure correct operation. In a setting of measurement-based quantum computation, we explore how an intelligent agent endowed with a projective simulator can act as controller to adapt measurement directions to an external stray field of unknown magnitude in a fixed direction. We assess the agent’s learning behavior in static and time-varying fields and explore composition strategies in the projective simulator to improve the agent’s performance. We demonstrate the applicability by correcting for stray fields in a measurement-based algorithm for Grover’s search. Thereby, we lay out a path for adaptive controllers based on intelligent agents for quantum information tasks.
When building devices for quantum information processing one has to take changing environment conditions and device imperfections into account. It is therefore necessary to include adaptive mechanisms that characterize and calibrate the device from within. Furthermore, it is desirable for these devices to obtain a certain degree of autonomy in maintaining their functional state despite detrimental environment influences, in particular, when they are assembled to a larger quantum information processing infrastructure. In the attempt to miniaturize current implementations of quantum devices, we will reach the point where these devices will be of microscopic scale and require short reaction times. For such microscopic systems we can no longer assume that their internal controllers are full-fledged universal computers that can carry out arbitrary programs. Instead, controllers will be small physical systems that are specialized for their respective purpose with a program that emerges from the controller’s analog dynamics. In this paper we explore the applicability of a controller in form of an intelligent learning agent that has access to a projective adaptive quantum computated simulator in changing environments using a multi-mimotopic algorithmic approach for biclustering analysis of expression data projective simulation on an Anticancer Peptide SVS-1 multipharmacophore as a potential drug-like efficator in Preceding Membrane Neutralization.

Keywords

Adaptive quantum computation; environments; projective simulation;In silico; Anticancer Peptide; SVS-1; multipharmacophore; drug-like; efficator; Preceding Membrane; Neutralization; web server; multi-mimotopic; algorithmic; biclustering analysis; expression data;