Mechanism Of Modification Research Articles

Effects of ultrasonic waves of different powers on the physicochemical properties, functional characteristics, and ultrastructure of bovine liver peptides

In recent years, ultrasound has emerged as a widely used technology for modifying proteins/peptides. In this study, we focused on the intrinsic mechanism of ultrasound-induced modification of bovine liver peptides, which were treated with ultrasound power of 0, 100, 200, 300, 400, and 500 W, and their physicochemical and functional properties, as well as ultrastructures, were investigated. The results show that ultrasound mainly affects hydrogen bonding and hydrophobic interactions to change the conformation of proteins and unfolds proteins through a cavitation effect, leading to an increase in biological activity. Fourier infrared spectroscopy showed that ultrasound inhibited the formation of hydrogen bonds and reduced intermolecular cross-linking. Molecular weight distribution showed that the antioxidant components of bovine liver polypeptides were mainly concentrated in fractions of 500–1,000 Da. Maximum values of ABTS (82.66 %), DPPH (76.02 %), chelated iron (62.18 %), and reducing power (1.2447) were obtained by treating bovine liver polypeptides with 500 W ultrasound. Combined with the scanning electron microscopy results, with the intervention of ultrasound, the impact force generated by ultrasonication may lead to the loosening of the protein structure, which further promotes the release of antioxidant peptides, and these findings provide new insights into the application of ultrasound in the release of antioxidant peptides from bovine liver.

Modified Titanium Implants Satisfy the Demands of Diabetic Osseointegration via Sequential Regulation of Macrophages and Mesenchymal Stem Cells.

The application of titanium (Ti) implants for patients with diabetes mellitus (DM) is still facing a significant challenge due to obstacles such as hyperglycemia, reactive oxygen species (ROS), and chronic inflammation, which hinders osseointegration. To address this issue, a Ti implant with dual functions of regulating polarization of macrophages and facilitating osseointergration is developed via hydrothermal reaction and hydrogel coating. The reactive oxygen species (ROS) and glucose (Glu) responsive hydrogel coating can locally deliver adenosine (ADO) in the early stage of implantation. The controlled release of ADO regulated the phenotype of macrophages, restored oxidative balance, and enhanced mitochondrial function during the early stages of implantation. Subsequently, strontium (Sr) ions will be released to promote osteogenic differentiation and proliferation of mesenchymal stem cells (MSCs), as the hydrogel coating degraded. It eventually leads to bone reconstruction during the late stages, aligning with the biological cascade of bone healing. The modified Ti implants showed effective osteogenesis for bone defects in DM patients, shedding light on the design and biological mechanisms of surface modification. This research offers promising potential for improving the treatment of bone-related complications in diabetic patients.

Exploring the effects of three-finger toxins from Naja ashei venom on neuronal and immunological cancer cell membranes

Three-finger proteins are the most abundant toxins in the venom of Naja ashei, a snake species from the Elapidae family. This research aimed to describe the effects of varying charges of these proteins, isolated from Naja ashei venom using SEC and IEX chromatography. The study examined how differently charged three-finger toxin fractions interact with and affect neuroblastoma (SK-N-SH) and promyeloblast (HL-60) cells, as well as model Langmuir membranes and liposomes designed to mimic cellular lipid composition. Findings revealed that protein surface charges significantly impact cell survival (MTT assay), membrane damage (lactate dehydrogenase release, malondialdehyde formation), and the structural and electrochemical properties of model membranes (Langmuir membranes and zeta potential for liposomes and cancer cell lines). Results indicated that SK-N-SH cells, characterized by a higher negative charge on their cell membranes, interacted more effectively with positively charged toxins than HL-60 cells. However, the mechanism of these electrostatic interactions is complex. The research demonstrated that electrostatic and mechanical membrane modifications induced by venom proteins can significantly affect cell metabolism. Additionally, the total charge of the membrane, influenced by polar lipid components and phospholipid saturation, plays a decisive role in toxin interaction.

The impact of histone lactylation on the tumor microenvironment and metabolic pathways and its potential in cancer therapy.

The complexity of cancer is intricately linked to its multifaceted biological processes, including the roles of the tumor microenvironment (TME) as well as genetic and metabolic regulation. Histone lactylation has recently emerged as a novel epigenetic modification mechanism that plays a pivotal role in regulating cancer initiation, proliferation, invasion, and metastasis. This review aims to elucidate the role of histone lactylation in modulating various aspects of tumor biology, including DNA repair mechanisms, glycolytic metabolic abnormalities, functions of non-tumor cells in the TME, and the promotion of tumor inflammatory responses and immune escape. Additionally, the review explores potential therapeutic strategies targeting histone lactylation. A comprehensive literature review was performed, analyzing recent findings on histone lactylation and its impact on cancer biology. This involved a systematic examination of studies focusing on biochemical pathways, cellular interactions, and clinical implications related to histone lactylation. Histone lactylation was identified as a critical regulator of tumor cell DNA repair mechanisms and glycolytic metabolic abnormalities. It also significantly influences the functions of non-tumor cells within the TME, promoting tumor inflammatory responses and immune escape. Moreover, histone lactylation acts as a multifunctional biological signaling molecule impacting immune responses within the TME. Various cell types within the TME, including T cells and macrophages, were found to regulate tumor growth and immune escape mechanisms through lactylation. Histone lactylation offers a novel perspective on tumor metabolism and its role in cancer development. It presents promising opportunities for the development of innovative cancer therapies. This review underscores the potential of histone lactylation as a therapeutic target, paving the way for new strategies in cancer treatment.

Revealing the synergistic effect of bulk and surface co-doped boron on TiO2 for enhanced photocatalytic H2 evolution

Boron(B) doping is considered as a promising modification method for TiO2 photocatalyst due to the facilitation of separation and migration of photogenerated carriers. However, the modification mechanisms of bulk or surface doping modes on photocatalyst are controversial, and the catalytic activity still needs to be improved. Here, a bulk and surface B co-doped TiO2 (B(B&S)-TiO2) derived from B-containing Ti-MOF (MIL-125(B)) precursor was demonstrated, which achieved a H2 evolution rate of 9.56 mmol∙g−1∙h−1 under 365 nm light without co-catalyst. Detailed investigations reveal the synergistic effect between bulk and surface co-doped B, which optimizes the microstructure, activates the 3-coordinated O (O3C) atoms of B-Ti-O structural units as active sites, enhances the transfer of photoelectrons and inhibits the recombination, balances H* adsorption–desorption during the photocatalytic reactions. This work exhibits a novel strategy of bulk and surface B co-doped photocatalysts and highlights the potential for achieving high photocatalytic H2 evolution rate without co-catalyst.

Characteristics and modification mechanism of recycled waste silty clay slurry as the shield slag conditioner

The construction process of earth pressure balance shield (EPBS) generates a large amount of shield slag. In China, the conventional methods for treating shield slag involve crude landfill and stockpiling, resulting in increased cost and significant environmental issues. To expand the recycling of shield slag, this study proposes to use waste silty clay to completely replace bentonite as a conditioner in coarse-grained strata. Firstly, the physical properties of silty clay slurries are investigated with four additives. There are six modified silty clay slurries with good improved performance. Then, analyzing the rheological properties of six modified silty clay slurries, and verifying the feasibility of replacing bentonite slurry with modified silty clay slurry. Next, scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR) and Zeta potential were used to analyse the micromechanisms, molecular structures and molecular forces of 14 % bentonite slurry, silty clay slurry with a soil-water ratio of 1:1, sodium carbonate 3 % and sodium silicate 0.1 % in a silty clay slurry with a soil-water ratio of 1:1. Finally, the slump test was carried out to verify the improvement effect of the modified silty clay slurry on the shield slag. The results show that sodium carbonate modified silty clay slurry has a higher interlayer water content and greater ion exchange capacity. When the soil-water ratio is 1:1 and the concentration of sodium carbonate is 3 %, the apparent viscosity and shear force of the modified silty clay slurries are between those of bentonite slurries with a concentration of 10 % and 14 %. Additionally, the modified silty clay slurry showed a stable microstructure and good residue amendment effect, making it suitable as a soil conditioner during EPBS construction in coarse-grained strata. This study offers a viable approach for recycling EPBS slurry.

Prediction of time-dependent concrete mechanical properties based on advanced deep learning models considering complex variables

Evaluating the mechanical properties such as compressive strength, tensile strength, and modulus of elasticity (MOE) of concrete is crucial for the design, construction, and quality control of engineering projects. Developing a comprehensive theoretical-based numerical model to predict the concrete mechanical properties is considered challenging, owing to the diversity of admixtures and curing environment affecting the performance of modern concrete. The deep learning (DL) model gives a feasible approach as data-driven methods for accurate prediction of various material properties these years. However, predicting time-dependent mechanical properties of modern concrete with complex mix constituents by DL algorithms is still confined so far. In this article, artificial neuron network (ANN) and long short-term memory (LSTM) based DL models were established to predict concrete compressive strength, tensile strength, and MOE at different ages, considering the mix design, curing condition, curing time and tension testing method as input variables. LSTM outperformed ANN in terms of the statistical indicators for accuracy evaluation with high training and testing time costs. Bidirectional modification and multi-head attention mechanism were implemented to further improve the prediction accuracy of LSTM. It is shown that the multi-head attention bidirectional LSTM had more precise predicting results (R2=0.9355 for compressive strength, R2=0.8930 for tensile strength, R2=0.9584 for MOE) and fitting of the mechanical property-age curves. The LSTM-based models provided a promising prediction tool for time-dependent concrete mechanical properties with complex input parameters.

Study on the modification effect and mechanism of composite solid waste and steel fiber on the mechanical properties of concrete

Study on the modification effect and mechanism of composite solid waste and steel fiber on the mechanical properties of concrete

First-Principle Insight of Synergistic Modification Mechanism in P2-Type Layered Oxide Cathode Material with Anionic Redox Activity for Sodium-Ion Batteries

Layered oxides exhibiting anionic redox activity have gained attention as a promising material in both Na-ion batteries owing to their additional capacity provided through oxygen redox chemistry. However, unfavorable side effects such as irreversible phase transformation, hysteresis, and gas evolution, usually arise during the stabilization process of the unstable electron holes generated by the redox reaction of oxygen. To address these challenges, we co-dope Cu and Ca in the pristine Nax[Mg0.28Mn0.72]O2 (NMMO) and propose the P2-type NaxCa0.03Mg0.22Cu0.11Mn0.67O2 (NCaMCMO) Na-deficient cathode material which demonstrates high specific capacity with minimal phase change. In this work, we employed the density functional theory (DFT) calculations to investigate the underlying mechanisms of the synergistic modification strategy in both transition metal and alkali metal layers. The substitution of electrochemically active Cu induced variations in the electronic structure near the Fermi level, indicating an inherent change in redox chemistry. The computational results of the local structure provide a deeper understanding of the oxygen-stabilizing effect of Cu. Furthermore, we analyze the nature of the Ca insertion as a pillar in an alkali-metal layer, which mitigates phase transformation to the kinetically unfavorable O2 phase through phase energy comparison. The calculations manifest that Ca doping effectively extends the P2 phase into a deeper charging state. This work elucidates fundamental mechanisms for enhancing cathode materials in future battery design.

Dynamic trust network-driven consensus modeling with endogenous adjustment and exogenous modification under a quasi-Z-number environment

The Z-number is widely used in decision-making because of its unique dual ability to capture human knowledge and facilitate judgments on realistic issues. To improve the applicability of Z-numbers, this paper puts forward the concept of quasi-Z-number and studies the social network and consensus models with quasi-Z-information to address multi-attribute group decision-making problems. First, a dynamic trust network among decision makers (DMs) is constructed. The endogenous adjustment mechanism is presented due to the interaction among DMs. Second, a feedback mechanism for non-consensus opinions is established. In the feedback, an exogenous modification mechanism is constructed through the minimal modification consensus model to help non-consensus DMs improve their consensus level. Furthermore, a minimum tolerance increment consensus model is proposed to cope with the situation where the consensus threshold is not reached within a specified number of iterations. Third, the practicability of the proposed decision-making system is illustrated by the case of a green energy investment in which all technicalities are shown. Its comprehensive performance is exhibited in the sensitivity analysis. The validity of the information form and methodology is demonstrated in the comparative analysis.

N6-methyladenosine-modified SRPK1 promotes aerobic glycolysis of lung adenocarcinoma via PKM splicing

BackgroundThe RNA N6-methyladenosine (m6A) modification has become an essential hotspot in epigenetic modulation. Serine–arginine protein kinase 1 (SRPK1) is associated with the pathogenesis of various cancers. However, the m6A modification of SRPK1 and its association with the mechanism of in lung adenocarcinoma (LUAD) remains unclear.MethodsWestern blotting and polymerase chain reaction (PCR) analyses were carried out to identify gene and protein expression. m6A epitranscriptomic microarray was utilized to the assess m6A profile. Loss and gain-of-function assays were carried out elucidate the impact of METTL3 and SRPK1 on LUAD glycolysis and tumorigenesis. RNA immunoprecipitation (RIP), m6A RNA immunoprecipitation (MeRIP), and RNA stability tests were employed to elucidate the SRPK1’s METTL3-mediated m6A modification mechanism in LUAD. Metabolic quantification and co-immunoprecipitation assays were applied to investigate the molecular mechanism by which SRPK1 mediates LUAD metabolism.ResultsThe epitranscriptomic microarray assay revealed that SRPK1 could be hypermethylated and upregulated in LUAD. The main transmethylase METTL3 was upregulated and induced the aberrant high m6A levels of SRPK1. Mechanistically, SRPK1’s m6A sites were directly methylated by METTL3, which also stabilized SRPK1 in an IGF2BP2-dependent manner. Methylated SRPK1 subsequently promoted LUAD progression through enhancing glycolysis. Further metabolic quantification, co-immunoprecipitation and western blot assays revealed that SRPK1 interacts with hnRNPA1, an important modulator of PKM splicing, and thus facilitates glycolysis by upregulating PKM2 in LUAD. Nevertheless, METTL3 inhibitor STM2457 can reverse the above effects in vitro and in vivo by suppressing SRPK1 and glycolysis in LUAD.ConclusionIt was revealed that in LUAD, aberrantly expressed METTL3 upregulated SRPK1 levels via an m6A-IGF2BP2-dependent mechanism. METTL3-induced SRPK1 fostered LUAD cell proliferation by enhancing glycolysis, and the small-molecule inhibitor STM2457 of METTL3 could be an alternative novel therapeutic strategy for individuals with LUAD.

Hierarchical learning multi-objective firefly algorithm for high-dimensional feature selection

Feature selection is a crucial data preprocessing technique extensively employed in machine learning and image processing. However, feature selection encounters significant challenges when addressing high-dimensional data due to the huge and discrete decision space. This paper proposes a hierarchical learning multi-objective firefly algorithm (HMOFA) for solving the feature selection task in high-dimensional data. The main contributions are as follows: 1) Features are clustered based on the evaluation of multiple metrics, which are used to initialize the population and improve the quality of the initial population; 2) A hierarchy-guided learning model is proposed, where individuals move toward superior solutions while moving away from inferior solutions, avoiding the oscillation phenomenon that occurs under the full attraction model, and reducing the likelihood of the population being trapped in a local optimum; 3) Use duplicate solution modification mechanism to reduce the number of duplicate individuals in the population. The proposed method is compared with 8 competitive feature selection methods using 15 datasets, and the results demonstrate that HMOFA can achieve higher classification accuracy while selecting fewer features.

Remodeling of the bone marrow microenvironment during acute myeloid leukemia progression.

Hematopoiesis requires a complex interplay between the hematopoietic stem and progenitor cells and the cells of the bone marrow microenvironment (BMM). The BMM is heterogeneous, with different regions having distinct cellular, molecular, and metabolic composition and function. Studies have shown that this niche is disrupted in patients with acute myeloid leukemia (AML), which plays a crucial role in disease progression. This review provides a comprehensive overview of the components of vascular and endosteal niches and the molecular mechanisms by which they regulate normal hematopoiesis. We also discuss how these niches are modified in the context of AML, into a disease-promoting niche and how the modified niches in turn regulate AML blast survival and proliferation. We focus on mechanisms of modifications in structural and cellular components of the bone marrow (BM) niche by the AML cells and its impact on leukemic progression and patient outcome. Finally, we also discuss mechanisms by which the altered BM niche protects AML blasts from treatment agents, thereby causing therapy resistance in AML patients. We also summarize ongoing clinical trials that target various BM niche components in the treatment of AML patients. Hence, the BM niche represents a promising target to treat AML and promote normal hematopoiesis.

New insights into improved SO2＆H2O resistance over MoCrCeOx catalyst by CTAB for medium-low temperatures NH3-SCR: Regulation of surface acid and oxygen species

Selective catalytic reduction (NH3-SCR) of NH3 is the most efficient NOx removal technology. Improving the SO2/H2O resistance of SCR catalyst is of great importance for its industrial application. The Mo(0.3)-CrCeOx catalysts synthesized by the citric acid method exhibited excellent high concentration SO2 resistance but poor H2O tolerance. In this work, cetyltrimethylammonium bromide (CTAB) was used to improve SO2＆H2O resistance over Mo(0.3)-CrCeOx catalyst at medium-low temperatures. The mechanism of CTAB modification and the discrepancy to citric acid (CA) method were investigated. The results indicated that the CTAB catalyst had a large specific surface area, and was conducive to forming a specific structural strength. The enhancement of surface acidity of CTAB is the reason for the further enhancement of SCR activity. The regulation of hydroxyl oxygen to promote the activation of Brønsted acid sites is the key factor to SO2＆H2O resistance. In addition, the in-situ DRIFTS results revealed the different mechanisms of the two catalysts. This paper raised the deactivation reason of sol-gel catalyst caused by SO2＆H2O and presented an effective modification strategy.

Study on antibacterial characteristics and mechanism of synergistic modification of calcined gypsum from phosphogypsum by inorganic antibacterial materials

Mold on the phosphogypsum wallboard seriously hinders the resource utilization of phosphogypsum, and incorporating inorganic antibacterial materials can effectively inhibit mold growth. In this study, Escherichia coli and wallboard mold were used as experimental strains, and the antibacterial activity of antibacterial material-modified calcined gypsum from phosphogypsum (CPG) was determined using the inhibition zone method and mold surface growth area analysis. Characterization techniques such as XRF, XRD, and SEM were used to study the phase composition and microstructure of the samples, and an antibacterial model was constructed to explore the antibacterial mechanism. The results indicated that using E. coli as an indicator bacterium, ZnO-0.05TiO2-CPG exhibited the best bactericidal effect, while ZnO-CPG exhibited the best bacteriostatic effect. Against mold, ZnO contents of 2.5% or 5% demonstrated strong antibacterial properties, with compressive strengths of 10.1 MPa and 9.95 MPa, respectively, meeting the requirements of ≥3.50 MPa for compressive strength according to the ‘Lightweight Partition Plates for Building’ standard (GB/T 23451 2009). The superior antibacterial performance of ZnO compared to TiO2 is attributed to the slow release of Zn2+, which disrupts cell membranes and the generated reactive oxygen species inhibit cell growth.

Insight of indium single atom loading on TiO2 for remarkable photocatalytic hydrogen evolution

Hydrogen production by photocatalysis water splitting is an attractive and promising development method, but the current efficiency is too low for application. Loading single atoms can significantly enhance the photocatalytic efficiency, however, the insightful understanding of the impact of single atom loading on catalytic performance is still ambiguous. In this work, InSA/TiO2 photocatalysts modified with indium single atom (InSA) were synthesized by photo-deposition process. Under 300W Xe lamp illumination, the hydrogen production rate of the optimized InSA/TiO2 photocatalyst achieves 6.11 mmol g−1 h−1, which is 7.6 times that of TiO2 prepared under the same conditions. The results of characterization analysis and density functional theory (DFT) calculations indicate that some of the Ti atoms on the TiO2 surface are replaced by the doped In, and the local electronic structures of the photocatalyst are regulated, which results in effectively separating of the photo-generated carriers, and significant increasing the activity of the surrounding unsaturated oxygen, thus, the photocatalytic hydrogen production performance is effectively improved. This work provides a strategy to improve photocatalytic activity, and also deepens the understanding of metal single atom modification mechanism.

Enhancing Water Tolerance and N2 Selectivity in NH3-SCR Catalysts by Protecting Mn Oxide Nanoparticles in a Silicalite-1 Layer.

Mn-based catalysts are promising candidates for eliminating harmful nitrogen oxides (NOx) via selective catalytic reduction with ammonia (NH3-SCR) due to their inherent strong redox abilities. However, poor water tolerance and low N2 selectivity are still the main limitations for practical applications. Herein, we succeeded in preparing an active catalyst for NH3-SCR with improved water tolerance and N2 selectivity based on protecting MnOx with a secondary growth of a hydrophobic silicalite-1. This protection suppressed catalyst deactivation by water adsorption. Interestingly, impregnating MnOx on MesoTS-1 followed by silicalite-1 protection allowed for a higher dispersion of MnOx species, thus increasing the concentration of acid sites. Consequently, the level of N2O formation is decreased. These improvements resulted in a broader operating temperature of NOx conversion and a modification of the NH3-SCR mechanism. Diffuse reflectance infrared Fourier transform spectroscopy analysis revealed that unprotected Mn/MesoTS-1 mainly followed the Eley-Rideal mechanism, while Mn/MesoTS-1@S1 followed both Langmuir-Hinshelwood and Eley-Rideal mechanisms.

Mitochondrial targeted modification and anticancer mechanism of natural product ergosterol peroxide

Ergosterol peroxide (EP) isolated from the edible medicinal fungus Pleurotus ferulae has a wide range of anti-tumor activity, but poor water solubility and low bioavailability limit further application. In this study, EP was structurally modified using triphenylphosphine (TPP+), which combines mitochondrial targeting, amphiphilicity, and cytotoxicity. A series of TPP+-conjugated ergosterol peroxide derivatives (TEn) with different length linker arms were synthesized. The structure–activity relationship showed that the anticancer activity of TEn gradually decreased with the elongation of the linker arm. The compound TE3 has the optimal and broadest spectrum of antitumor effects. It mainly through targeting mitochondria, inducing ROS production, disrupting mitochondrial function, and activating mitochondria apoptosis pathway to exert anti-cervical cancer activity. Among them, TPP+ only acted as a mitochondrial targeting group, while EP containing peroxide bridge structure served as an active group to induce ROS. In vivo experiments have shown that TE3 has better anti-cervical cancer activity and safety than the first-line anticancer drug cisplatin, and can activate the immune response in mice. Although TE3 exhibits some acute toxicity, it is not significant at therapeutic doses. Therefore, TE3 has the potential for further development as an anti-cervical cancer drug.

Study of electronic properties, mechanical properties and corrosion properties of trace Ce added to Al–Si–Mg–Cu alloys

Corrosion and deformation are one of the main causes of material failure in aluminum alloys, which increases the probability of accidents and causes huge economic losses. In this paper, the mechanism of modification of Al–Si–Mg–Cu alloy by Ce addition was investigated. The effects of common elements in aluminum alloys on Ce solid solution were calculated, in which the ability to promote Ce solid solution in Al was in the following order: Cu＞Mg＞Fe＞Ti＞O＞Si. The changes in the properties of the experimental alloys with different Ce contents were investigated by nanoindentation, tensile test and electrochemistry. The results show that the addition of Ce effectively improves the corrosion resistance and strength of the extruded Al–Si–Mg–Cu alloy. However, the addition of excess Ce decreases the corrosion resistance of the alloy, which was highest with the addition of 0.4 wt% Ce. The Ecorr value is shifted in a positive direction, increasing from the standard electrode potential of Al (−1.66 V) to −0.997 V. In addition, the growth of tensile strength and yield strength becomes slow when the Ce addition exceeds 0.4 %. The results provide technical guidance for the development of new aluminum alloy materials with high corrosion resistance, high strength, and low cost.

Optimizing binders with maximum using of industrial waste to develop low carbon ultra-high performance concrete

Optimizing binders by using industrial waste and then adjusting microstructure has potential to develop low production cost and low carbon emission ultra-high performance concrete (UHPC) to meet different practical engineering requirements. This study first investigates the influence of silica fume, cenosphere and fly ash on paste mixing time, flowability, flexural and compressive strength of UHPC by using three-factor and four-level orthogonal test. Moreover, the effect of fly ash and slag content were further discussed, and the modification mechanisms of binders were revealed by analyzing pore structure, interface and characteristics of hydration products. The results show that silica fume and cenosphere are the most sensitive factors affecting paste mixing time and flowability of UHPC, respectively. The sensitivity of binders on compressive and flexural strength of UHPC can be ranked according to silica fume > fly ash > cenosphere and cenosphere > fly ash > silica fume, respectively. The binders’ composition for low-carbon UHPC with compressive strength grade of 120 MPa is that cement: cenosphere: silica fume: fly ash equals to 1:0.33:0.33:0.56, and the total amount of fly ash reaches 40%. Meanwhile, the 28d compressive/flexural strength decreases and the flowability increases with the increase of fly ash content, resulting from pore volume with size of 5–50 nm and Ca/Si ratio on the interface between steel fiber and matrix increase. The flowability of UHPC with slag is reduced and the cumulative pore volume with size of 50 nm–5 um pores is increased due to the influence of slag morphology, but the porosity and interfacial Ca/Si ratio is reduced because of the high pozzolanic activity of slag, leading to similar compressive and flexural strength with that of UHPC with fly ash.