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At least 19 recordsLinked to original sources

A reinforcement learning-enhanced fuzzy multi-objective equilibrium optimization framework for multiple sequence alignment.

Multiple sequence alignment (MSA) is a fundamental task in bioinformatics, underpinning comparative genomics, structural analysis, and evolutionary inference. However, MSA remains a challenging multi-objective optimization problem due to the need to simultaneously maximize alignment accuracy, preserve conserved regions, and control gap proliferation, particularly in large and heterogeneous sequence collections. In this work, we propose MOFSACEO-MSA, a novel hybrid optimization framework for multiple sequence alignment that integrates a fuzzy multi-objective evaluation scheme with the Equilibrium Optimizer (EO) and a Soft Actor-Critic (SAC)-based adaptive control mechanism. The proposed framework formulates MSA as a dynamic multi-objective optimization problem, in which alignment quality is assessed using complementary residue-level and column-level criteria, including Sum-of-Pairs score, column conservation, entropy, and gap statistics. Fuzzy membership functions are employed to harmonize competing objectives into a unified optimization landscape, while EO provides robust global exploration. To further enhance adaptability, SAC dynamically regulates key EO parameters during the search process, enabling an effective balance between exploration and exploitation across datasets of varying size and heterogeneity. Extensive experiments werew conducted on diverse biological sequence datasets, with a primary focus on RNA benchmarks, including structured families from Rfam, large-scale repositories from RNAcentral and GenBank, and organism-specific tRNA datasets from GtRNAdb. Comparative evaluations against classical alignment tools (ClustalW, MAFFT, MUSCLE, PRANK, KAlign, and T-Coffee), metaheuristic methods (SAGA, Sequoya and EAFSA), and a reinforcement learning-based approach (RLALIGN) demonstrate that MOFSACEO-MSA consistently achieves competitive or superior Sum-of-Pairs scores while significantly reducing gap proportions and maintaining compact alignment lengths. Notably, the proposed framework exhibits improved robustness on large and highly heterogeneous datasets, where existing methods often suffer from excessive gap insertion or unstable convergence. Overall, MOFSACEO-MSA provides a flexible and extensible optimization paradigm that effectively bridges evolutionary search and reinforcement learning for high-quality multiple sequence alignment, with demonstrated effectiveness on challenging RNA alignment tasks.

Sequence Alignment↗

Surface Complexation Modeling of Organic Acid Sorption to Goethite.

Surface complexation modeling was performed using the Generalized Two-Layer Model for a series of low molecular weight organic acids. Sorption of these organic acids to goethite was investigated in a previous study to assess the influence of particular structural features on sorption. Here, the ability to describe the observed sorption behavior for compounds with similar structural features using surface complexation modeling was investigated. A set of surface reactions and equilibrium constants yielding optimal data fits was obtained for each organic acid over a range of total sorbate concentrations. Surface complexation modeling successfully described sorption of a number of the simple organic acids, but an additional hydrophobic component was needed to describe sorption behavior of some compounds with significant hydrophobic character. These compounds exhibited sorption behavior that was inconsistent with ligand exchange mechanisms since sorption did not decrease with increasing total sorbate concentration and/or exceeded surface site saturation. Hydrophobic interactions appeared to be most significant for the compound containing a 5-carbon aliphatic chain. Comparison of optimized equilibrium constants for similar surface species showed that model results were consistent with observed sorption behavior: equilibrium constants were highest for compounds having adjacent carboxylic groups, lower for compounds with adjacent phenolic groups, and lowest for compounds with phenolic groups in the ortho position relative to a carboxylic group. Surface complexation modeling was also performed to fit sorption data for Suwannee River fulvic acid. The data could be described well using reactions and constants similar to those for pyromellitic acid. This four-carboxyl group compound may be useful as a model for fulvic acid with respect to sorption. Other simple organic acids having multiple carboxylic and phenolic functional groups were identified as potential models for humic substances. Copyright 1999 Academic Press.

Journal Article↗

[Posologic equivalents of oral L-thyroxine in thyroid insufficiency (120 cases)].

The effects of two successive courses of thyroid replacement therapy in the same patients can be compared by measuring plasma hormone levels at the steady state. This method was used to assess the effects of the two forms of oral L-thyroxine, the one in liquid drops 5 micrograms/drop and the other in 50 and 100 micrograms tablets, and to compare these preparations with other forms of thyroid replacement therapy: DL T4, LT3 + LT4 and thyroid extract. The bioequivalence of these drugs was determined by the logarithmic difference of the plasma TSH during successive treatment periods. In addition, this factor could be assessed by the ratios of circulating T4 to T3 when the two treatment periods were identical. One 100 micrograms tablet of L-thyroxine was equivalent to 20 drops of L-thyroxine (100 micrograms), i.e. the bioavailability of the two preparations was identical. This dose was equivalent to three drops of DL thyroxine (i.e. 100 micrograms of L-thyroxine): the D-thyroxine did not have any demonstrable hormonal properties. The same dose was equivalent to about 3/4 of a tablet of LT3 + LT4, and to about 12 cg of thyroid extract. Individual stabilisation with L-thyroxine in cases of peripheral thyroid deficiency was based on basal TSH levels and TSH levels after injection of TRH when the basal TSH was normalised. The plasma T3 and T4 levels could also be used for optimal equilibrium with L-thyroxine; the first should be within the normal range and the second in the normal or mildly hyperthyroid range. The optimal adult dose of L-thyroxine in this study was variable (115 +/- 40 micrograms/day). In young children, especially babies, the effective dose with respect to body weight, is much greater.

Administration, Oral↗

A problem of optimal harvesting policy in two-stage age-dependent populations.

The optimal equilibrium harvesting policy is investigated for an age-dependent population of females whose life history consists of two stages termed eggs (or juveniles) and adults. Using a continuous-time linear model, we consider admissible harvesting policies in which a certain fraction of individuals of fixed ages is harvested per unit time in both stages to bring the population to an equilibrium level. Determination of the harvest rate that maximizes the sustainable yield, subject to a linear ecological or economic constraint, leads to a nonlinear, nonconvex optimization problem. The optimal policy is shown to consist of harvesting at most three ages. Thus, we say that the harvest is trimodal. In one stage, at most two ages are harvested, with the oldest being harvested completely; in the other, at most one age is harvested completely. In each stage, the age totally removed, if present, is older than the surplus age, which is the age at which the proportion of the expected number of eggs multiplied by the proportion of the expected number of adults first exceeds one. The three harvesting ages are dependent on the birth, maturation, and death rates and on the economic parameters of the problem. A simple algorithm to find the optimum harvesting strategy is described.

Age Factors↗

The heaviest group 2 Difluoride, RaF(2): geometry and ionization energy.

The heaviest group 2 difluoride, radium difluoride (RaF(2)), is studied for the first time. A basis set is employed for radium that combines an effective core potential with a large, flexible valence space. This basis set is tested by calculating the first and second ionization energies of Ra, where values in excellent agreement with experiment are obtained. MP2 ab initio calculations are employed to obtain the optimized equilibrium geometry and the harmonic vibrational frequencies for the ground-state neutral and some of the low-lying cationic states. In addition, the optimized geometry of the ground-state neutral is obtained at the CCSD(T) level. The trend in geometry of the group 2 difluorides is confirmed, with an angle FRaF bond angle of 118 degrees being calculated, together with a bond length of 2.30 A. It is concluded that involvement of the Ra 6p orbitals in the valence molecular orbitals of RaF(2) adequately explains its bent geometry. RCCSD(T) calculations are then employed to calculate ionization energies. The first adiabatic ionization energy, corresponding to the ionization (tilde)X(2)Sigma(u)(+) <-- (tilde)X(1)A(1), is calculated to be 10.67 +/- 0.05 eV. The ordering of the ionic states is discussed in the light of the present results. The polarizability of Ra was calculated to be 36.3 A(3), with that of Ra(2+) was calculated to be 1.97 A(3); the latter was employed in a simple ionic model, but this failed to calculate the ionization energy accurately.

Journal Article↗

Analytical energy gradients for local second-order Møller-Plesset perturbation theory using density fitting approximations.

An efficient method to compute analytical energy derivatives for local second-order Møller-Plesset perturbation energy is presented. Density fitting approximations are employed for all 4-index integrals and their derivatives. Using local fitting approximations, quadratic scaling with molecular size and cubic scaling with basis set size for a given molecule is achieved. The density fitting approximations have a negligible effect on the accuracy of optimized equilibrium structures or computed energy differences. The method can be applied to much larger molecules and basis sets than any previous second-order Møller-Plesset gradient program. The efficiency and accuracy of the method is demonstrated for a number of organic molecules as well as for molecular clusters. Examples of geometry optimizations for molecules with 100 atoms and over 2000 basis functions without symmetry are presented.

Journal Article↗

Rapid and direct measurement of free concentrations of highly protein-bound fluoxetine and its metabolite norfluoxetine in plasma.

Fluoxetine (F) and its active N-demethylated metabolite, norfluoxetine (NF), are selective serotonin re-uptake inhibitors that bind extensively to plasma proteins. Development and validation of a novel method for measuring free concentrations of F and NF in plasma are reported here. The plasma filtrate was prepared by a high-speed short-duration ultrafiltration (UF) and then submitted directly to a short-column liquid chromatography/tandem mass spectrometric (LC/MS/MS) assay. There was no significant matrix effect on the analysis, and non-specific binding of the analytes to the UF devices was negligible. For validation of the method, the recovery of the free analytes was compared to that from an optimized equilibrium dialysis method, and analyte stability was examined under conditions mimicking the sample storage, handling, and analysis procedures. The linearity range was 0.37-12 ng/mL for F and NF; the within-run and between-run relative standard deviations were less than 11.9%, and accuracies across the assay range were 100 +/- 10.3%. This new method was then further validated in a pharmacokinetic (PK) study in beagle dogs receiving a single oral dose of fluoxetine hydrochloride. The integrity of the resulting PK data of free F and NF was absolute. The PK data indicate that the novel method is accurate and reliable. To our knowledge this is the first report describing a rapid and reliable method for direct measurement of free concentrations of F and NF in plasma, which will be useful for clinical pharmacokinetic/pharmacodynamic studies of F. Furthermore, the strategies described herein may be applied to the development and validation of methods for measuring the free concentrations of other drugs in plasma.

Animals↗

Partial characterization and ontogeny of renal cytosolic glucocorticoid receptors in mouse kidney.

The glucocorticoid receptor (GR) was partially characterized in mouse renal cytosol. A sensitive and reproducible [3H]dexamethasone binding assay suitable for use with small quantities of cytosolic protein, was developed. Studies defined the optimal equilibrium binding conditions, metabolism of [3H]dexamethasone in adult renal cytosol, specificity of binding of the GR, and molecular weight of the GR-[3H]dexamethasone complex by gel filtration chromatography. The assay was subsequently used to measure the renal GR during different stages of foetal and postnatal development, as well as in glomerular and renal tubular preparations from adult mice. An almost linear increase in GR occurred from day 13 to day 18 of gestation with levels rising from 100 to 201 fmol/mg cytosol protein; this was followed by a sharp rise in receptor concentration just after birth to 343 fmol/mg cytosol protein. Adult levels, 410-433 fmol/mg cytosol protein, were reached by 2 weeks after birth. The equilibrium dissociation constants (Kd) of the [3H]dexamethasone-receptor complex were similar in adult and in embryonic cytosols (range, 2.8-11.8 nM; mean +/- SD = 6.5 +/- 2.9 nM). Specific binding was assessed to be 3- to 5-fold greater in tubular than in glomerular preparations. These data on the localization and ontogeny of GR during murine metanephric development provide a basis for study of glucocorticoid-mediated effects on various models of congenital and acquired renal disease.

Aldosterone↗

Complexities in ETS-domain transcription factor function and regulation: lessons from the TCF (ternary complex factor) subfamily. The Colworth Medal Lecture.

The ETS-domain transcription factor family can be divided into a series of subfamilies. Elk-1 represents the founding member of the ternary complex factor (TCF) subfamily. By focusing on the TCF subfamily, we can demonstrate the complexities that exist in the function and regulation of ETS-domain transcription factors. This article focuses on Elk-1 in detail and summarizes the functions of other TCFs. The key themes covered include the domain structure of the TCFs, the mechanisms of complex formation with serum response factor, regulation of TCFs by mitogen-activated protein kinase cascades, and transcriptional regulatory properties of the TCFs. Finally, the emerging role of the TCFs in vivo is discussed. A picture is developing indicating that, while these proteins exhibit significant sequence and functional conservation, key differences in their structure and regulation are being identified which may relate to unique functions of these proteins in vivo.

Amino Acid Sequence↗

Co-ordination of a simple voluntary multi-joint movement with postural demands: trunk extension in standing man.

The interaction between primary movements and associated postural adjustments was studied during trunk extension movements in standing man. Six healthy male subjects performed one series of six consecutive fast trunk extensions. Movements were recorded with an optoelectronic system (Selspot). Angular displacements, velocities and accelerations at the ankle, knee, hip and trunk were calculated. Trunk inclination was measured as the sum of pelvic tilt and spine flexion. The spatial and temporal coordination patterns chosen by the subjects to complete the task were compared. The self-selected trunk movement amplitude ranged 14-30 degrees for all subjects. The individual amplitude was maintained within 4-7 degrees over the six consecutive trials. Peak velocity of the primary trunk movement was highly correlated with movement amplitude (r = 0.73, P less than 0.01), whereas peak acceleration was not. Trunk extension, was the result of a simultaneous backward pelvic tilt and spine extension, together with hip extension and knee flexion. Knee flexion became increasingly important at larger movement amplitudes since hip extension as well as spine extension was limited. Associated postural adjustments occurred mainly as ankle flexion. In conclusion, individuals can accurately reproduce the multi-joint co-ordination pattern seen during a voluntary trunk extension movement. Movements at the ankle appear to be controlled to counteract the backward shift of the centre of gravity caused by the primary movement. Knee and ankle movements seem to be independently controlled in the preparatory phase, whereas they are closely linked later during the primary movement. It is suggested that the interaction between knee and ankle movements is necessary for optimal equilibrium control during trunk extension movements in standing.

Adult↗

Galanin receptors in a hamster pancreatic beta-cell tumor: identification and molecular characterization.

High affinity binding sites for galanin are identified and characterized in membranes from a hamster pancreatic beta-cell tumor. Using the radioiodinated peptide [125I] galanin, interaction of the peptide with pancreatic membranes is shown to be saturable, reversible, and time, temperature, membrane protein concentration, pH, and ionic strength dependent. In optimized equilibrium conditions of binding (90 min at 10 C), native galanin competitively inhibits the binding of [125I]galanin in a dose-dependent manner (from 10(-11)-10(-8) M); half-maximal inhibition is induced by 1 nM peptide. Scatchard analysis indicates the existence of a single population of sites of high affinity (Kd = 1.5 nM) and low capacity (44 fmol/mg protein). The monophasic dissociation process confirms the homogeneity of galanin-binding sites. Galanin-binding sites are highly specific, since apart from native galanin, none of the numerous biologically active peptides tested competes with [125I] galanin for binding to pancreatic membranes. The cross-linking of [125I]galanin to beta-cell membranes is performed using the chemical bifunctional reagent ethylene glycol bis-(succinimidyl succinate). After sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis in the presence or absence of dithiothreitol, one single band of 57,000 mol wt is observed, which may be corresponding to the [125I]galanin-receptor complex. Indeed, labeling of this 57,000 mol wt component is abolished only by native galanin but is unaffected by various other digestive peptides. Assuming one molecule of [125I]galanin is bound per molecule of protein, a 54,000 mol wt protein is identified as the pancreatic galanin receptor. In conclusion, our results indicate for the first time the identification of galanin receptors. Their presence in pancreatic beta-cells suggests a direct role of galanin in regulating endocrine beta-cell function.

Adenoma, Islet Cell↗

[Altitude adaptation. Part III. Altitude acclimatization as a problem of human biology (II. Morphology, physiology, biochemistry)].

The physiological mechanisms of adaptation will be reported. In a primary step of adaptation, the body reacts with immediate response, which already leads to a first classification: whether or not altitude will be tolerated by an individual. More steady biological processes follow with the same intention of balancing oxygen deficiency. They may be successful and acclimatization is possible, or they do not achieve the necessary level, i.e. that consequently developing pathological conditions of different severity lead to a next assortation of individuals with insufficient adaptability. The first state of lability can be compensated, or the intolerance will make a further stay in high altitudes impossible. No parameters exist which could allow a prognosis as to what kind of individuals will tolerate altitude or not. A different pattern of biological reaction is seen in permanent inhabitants of high altitudes who have been residing there for generations and haven't experienced conditions other than those of their special altitude in their individual lives. While ascending to higher altitudes, permanent residents also have to undergo new adaptation, as well as when descending to lower altitudes. Returning to their native environment requires reacclimatization. The mechanisms of adaptation on the organ level will be reviewed, as well as on the fluid and cellular level. All those functional and morphological mechanisms of adaptation to oxygen deficiency in high altitudes tend to maintain optimal equilibrium. Maladaptation may result. Expected genetically determined physiological alterations of adaptational value in permanent residents, which could have manifested themselves by way of "soft" selection and change of gene frequency in those high altitude populations, will be discussed. Genetical determination in such physiological parameters does not seem probable, although some pecularities such as the "blunted response" ventilation, the higher Bohr-Effect in Quenchua etc. might be interpreted in this direction.

Acclimatization↗

[Altitude adaptation. V. (conclusion). Morbidity and mortality. Literature].

The ability to adapt to extreme conditions is a continously working principle of man's evolution, in a permanent orientation to an optimal equilibrium between man and environment. A paradigm of biological adaptation is the condition of hypoxia at high altitudes, as one of the few environment constellations to which a pure biological and thus genetically based answer could be possible. The majority of adaptations are influenced by technological actions, which partially modify the environment in compensating unfavourable constellations (heating, clothing, housing, etc.). It is discussed, how far the adaptation to high altitudes produces transitory or permanent alterations with reference to constitution, perseverance, cold-sensitivity, diseases, duration of life, fertility, course of pregnancy, adaptations at the organ- and tissue-level, blood-composition, fluid-equilibrium of the body etc., which guarantee the survival of the individual and its successful reproduction with regard to the continuance of a mendel population. The elucidation of the question on genetic determination of features characteristic for high altitude inhabitants is difficult because we know next to nothing about the genetic determination of physiologic parameters. Studies on ethnic marker-genes (Ethiopia, South-America) give no reference to population differences. Remarkable is a striking prevalence of the blood-group O for all populations of high altitudes, but one must consider the effects of isolation in terms of the increase in the homozygote recessive alleles. We can propose, that in the primary settlement at high altitudes a "hard selection" was working, a kind of biological assortation-process from the beginning, which eliminated those individuals, who proved to be (for genetic reasons?) not adaptable. A good example for this are observations of cattle, from which 50% do not develop pulmonary hypertension when exposed to altitude, that means they already have a higher initial fitness. The non-adaptable animals have to be returned to the lowlands. In the F1-generation only 2% of the animals remaining at high altitude, develop "brisket disease". Possibly that means a sort of "out-mendeling" of "pulmonary-hypertension-genes", which may manifest themselves in the condition of hypoxia. Also the good adaptation of llamas is partially due to the fact that the camelids per se possess an outstanding O2 affinity and morphologically different red blood cells, which predispose this species to inhabit high altitudes. Parallel to considerations like these it could be imaginable, that e.g. the indianids of mongoloids in general, are genetically composed as fit to inhabit lowlands as well as highlands, in contrast to caucasoids and negroids. The largest mountain areas of the world (the Andes: 12 X 10(6)), the Himalayas 12 X 10(6)) are inhabited by populations of mongoloid ancestry, for about 10,000 years, a period, which ought to be long enough to make possible genetic specialisation, although it is not yet possible to prove it...

Acclimatization↗

[Functional significance of a floating eye model].

The role of the floating eye model in the organization of situating and producing eye micromovements was studied. There is presented a hydromechanical model of orthophoria of latent and obvious squint. It is shown that the multiformity of obvious squint depends on the variety of combinations of nonuniform forces in the right eye aparting from the left one, which is the result of nonuniform deviations of both eyes from the norm, and heterophoria is the result of combinations of uniform forces aparting and of analogous deviations of both eyes form. It is shown that the concomittant squint is caused by the existence of different polar heterophoria at both eyes, and their multiformity is the result of their various combinations. The essential necessity of the eye floating for the organization of micromovements--eye tremor and drift is established. It is shown that the eye tremor which takes place under incomplete tetanus of the musole is possible only at optimal equilibrium of the eye and absence of friction they both are at floating. The non-muscle moving character of the eye drift is revealed. It proceeds under the influence of hydromechanical forces of aparting and nonequilibrated gravity of the cornea as a result of weakening of the eye movement muscle under fixation. The cause of the optic, axis divergence (OA) with optic line (OL) and the necessity with it of postnatal development of the eye dioptrics under active influence of the motor apparatus was discovered. Physiology of the eye floating, new conclusions and a hypothesis concerning the model are discussed.

Biomechanical Phenomena↗

Monoclonal antibody-based dual-label time-resolved fluorometric assays in a simplified one-step format.

We have performed a one-step all-in-one dual-label dry reagent time-resolved fluorometric assay measuring free and total prostate-specific antigen (PSA). All assay-specific components were predried in an ordinary microtitration well, including the Eu and Tb chelate-labeled monoclonal antibodies for the recognition of free and total PSA, respectively. Only the sample and assay buffer needed to be added. Optimally, equilibrium was reached in <15 min. New intrinsically fluorescent Eu and Tb chelates were used, which made it possible to read the fluorescence directly from the solid phase. The developed dual-label assay with the simple protocol is ideal for easy automation, as the reaction wells can be of alternative design. The performance characteristics are equivalent to those of the present state-of-the-art single-label assays. The detection limits for free and total PSA were 0.03 and 0.02 microg/L, respectively, and the assays were linear over the range tested (up to 300 microg/L).

Antibodies, Monoclonal↗

Chemically blocked analog assays for free thyronines. II. Use of equilibrium dialysis to optimize the displacement by chemical blockers of T4 analog and T3 analog from albumin while avoiding displacement of T4 and T3 from thyroxin-binding globulin.

Chemical blockers used to displace thyronine analog from albumin in analog kits for assay of free thyroxin (FT4) or free triiodothyronine (FT3) may also displace thyroxin (T4) or triiodothyronine (T3) from thyroxin-binding globulin (TBG), resulting in an apparent TBG dependence of results of free hormone estimates. We used equilibrium dialysis and antibody binding to assess the displacement of thyronine analogs and thyronines from albumin and TBG by use of chemical blockers. We chose a combination of two chemical blockers, which eliminated thyronine analog-albumin binding but minimized thyronine displacement from TBG for use in FT4 and FT3 assays. These blocked-analog free-hormone assays yielded accurate clinical results in euthyroid patients, hypo- and hyperthyroid patients, and in pregnant women. FT4 results were not entirely normalized in all nonthyroidally ill patients, indicating that decreased analog-albumin binding is not the only factor resulting in low FT4 results. In current Diagnostic Products Corp. (DPC) FT4 and FT3 blocked-analog kits, the blocker concentrations are the same as we used in these assays.

Dialysis↗

Development of an automated photometric assay for serum lithium and use of binding equilibrium expressions to optimize results.

BACKGROUND: A spectrophotometric serum lithium assay and relevant reaction equilibria used in the assay development are described. METHODS: The dye, 7-nitro-2,12-dicarboxyl-16,17-dihydro-5H,15H-dibenzo[b,i] [1,11,4,5,7,8]dioxatetraazacyclotetradecine reacts rapidly with Li(+) in alkaline water/dimethylsulfoxide with an absorbance change. Sodium binds weakly, thus presenting potential inaccuracy from varying endogenous sodium. To minimize this problem, excess sodium ion was added from reagents. This diminishes the signal from lithium binding, thus lowering sensitivity, requiring selection of reagent sodium concentration for proper balance of performance characteristics. Absorptivities and binding constants were determined. Description of competing equilibria by an explicit cubic equation was used to predict sensitivity and effects of varying endogenous Na(+) concentration as functions of added NaCl. RESULTS: Concentration-absorbance data were satisfactorily predicted by the cubic equation, equilibrium constants, and absorptivities. Li(+) binds 300 times more tightly than Na(+). Interference was minimized, while sufficient sensitivity for needed precision was retained. A full evaluation is summarized separately in this issue. CONCLUSIONS: Explicit description of the competitive binding was successfully used to develop an automated liquid reagent assay for Li(+) with acceptable accuracy and precision.

Automation↗