• 한국수소및신에너지학회논문집
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• 제23권6호
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• pp.654-659
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• 2012

The interest in water gas shift (WGS) reaction has grown significantly, as a result of the recent advances in fuel cell technology and the need to develop small-scale fuel processors. Recently, researchers have tried to overcome the disadvantages of the commercial WGS catalysts. As a consequence, supported Pt catalysts have attracted a lot of researchers due to high activity and stability for WGS at low temperatures. In this study, $Pt-Na/Ce_{(1-x)}Zr_{(x)}O_2$ catalysts with various Ce/Zr ratio have been applied to WGS at a gas hourly space velocity (GHSV) of $45,515h^{-1}$. According to TPR patterns of $Pt-Na/Ce_{(1-x)}Zr_{(x)}O_2$ catalysts, the reducibility increases with decreasing the $ZrO_2$ content. As a result, Cubic structure $Pt-Na/Ce_{(1-x)}Zr_{(x)}O_2$ catalysts exhibited higher CO conversion than tetragonal structure $Pt-Na/Ce_{(1-x)}Zr_{(x)}O_2$ catalysts. Expecially, Pt-Na/$CeO_2$ exhibited the highest CO conversion as well as 100% selectivity to $CO_2$. Moreover, Pt-Na/$CeO_2$ catalyst showed relatively stable activity with time on stream. The high activity of cubic structure Pt-Na/$CeO_2$ catalyst was correlated to its higher oxygen storage capacity (OSC) of $CeO_2$ and easier reducibility of Pt/$CeO_2$.

• BMB Reports
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• 제53권3호
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• pp.166-171
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• 2020

A chemical library comprising 2,354 drug-like compounds was screened using a transcription and replication-competent viruslike particle (trVLP) system implementing the whole Ebola virus (EBOV) life cycle. Dose-dependent inhibition of Ebola trVLP replication was induced by 15 hit compounds, which primarily target different types of G protein-coupled receptors (GPCRs). Based on the chemical structure, the compounds were divided into three groups, diphenylmethane derivatives, promazine derivatives and chemicals with no conserved skeletons. The third group included sertindole, raloxifene, and ibutamoren showing prominent antiviral effects in cells. They downregulated the expression of viral proteins, including the VP40 matrix protein and the envelope glycoprotein. They also reduced the amount of EBOV-derived tetracistronic minigenome RNA incorporated into progeny trVLPs in the culture supernatant. Particularly, ibutamoren, which is a known agonist of growth hormone secretagogue receptor (GHSR), showed the most promising antiviral activity with a 50% effective concentration of 0.2 μM, a 50% cytotoxic concentration of 42.4 μM, and a selectivity index of 222.8. Here, we suggest a strategy for development of anti-EBOV therapeutics by adopting GHSR agonists as hit compounds.

• Bulletin of the Korean Chemical Society
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• 제31권9호
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• pp.2509-2513
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• 2010

In order to increase protease stability of a novel Trp-rich model antimicrobial peptide, $K_6L_2W_3$ (KLWKKWKKWLK-$NH_2$)and investigate the effect of L-amino acid to peptoid residue conversion on biological functions, we synthesized its antimicrobial peptoid, $k_6l_2w_3$. Peptoid $k_6l_2w_3$ had similar bacterial selectivity compared to peptide $k_66L_2W_3$. The bactericidal rate of $k_6l_2w_3$ was somewhat slower than that of $K_6L_2W_3$. Peptoid $k_6l_2w_3$ exhibited very little dye leakage from bacterial outer-membrane mimicking PE/PG liposomes, as observed in $K_6L_2W_3$, indicating that the major target site of $K_6L_2W_3$ and $k_6l_2w_3$ may be not the cell membrane but the cytoplasm of bacteria. Trypsin treatment of $K_6L_2W_3$ completely abolished antimicrobial activities against Escherichia coli and Staphylococcus aureus. In contrast, the antimicrobial activity of $k_6l_2w_3$ was completely preserved after trypsin treatment. Taken together, our results suggested that antimicrobial peptoid $k_6l_2w_3$ can potentially serves as a promising therapeutic agent for the treatment of microbial infection.

• 약학회지
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• 제51권5호
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• pp.313-317
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• 2007

A series of luotonin A homologues and their aza-analogues were prepared and evaluated their inhibitory activities on COX-1 and 2 as well as their selectivities on COX-2. The aza-analogue of dimethylene-bridged homologue of luotonin A, 3,3'-dimethylene-2-(1',8'-naphthyrid-2'-yl)-4(3H)-quinazolinone (2b), exhibited strongest inhibitory activity against COX-1 and COX-2 dependent phase of prostaglandin $D_2$ generation in mouse bone marrow-derived mast cells in a concentration-dependent manner with an $IC_{50}$ of 39.3 and $1.89{\mu}M$, respectively. Selectivity of 2b on COX-2 over COX-1 was 21 which implied 2b can be a potential lead for the development of selective COX-2 inhibitor.

• 멤브레인
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• 제21권3호
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• pp.247-255
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• 2011

본 연구에서는 뛰어난 전도도와 물리적 강도를 가지는 그라핀의 고른 분산성을 얻기 위하여 두 가지 다른 방법으로 그라핀을 개질시켰다. 그리고 SPAES/그라핀 복합막은 각기 다른 함량을 첨가하여 제조되었으며 그라핀의 제조방법과 첨가된 그라핀의 함량에 따른 성능을 비교하였다. 복합막의 모폴로지는 SEM을 이용하여 관찰하였으며 개질된 그라핀의 화학적 구조는 FT-IR과 TGA를 사용하여 분석되었다. 그라핀의 함량변화가 0.5~3.0 wt% 일 때 복합막의 이온전도도와 메탄올 투과도를 측정하였으며 $80^{\circ}C$, 100% 가습상태에서 SPAES/그라핀 복합막의 이온전도도(0.216 S/cm)는 순수한 SPAES 전해질 막보다 높은 이온전도도(0.098 S/cm)를 나타내었으며 그라핀의 함량이 1.5 wt%까지 증가될 때 메탄올 투과도는 감소되었다.

• Journal of the Korean Wood Science and Technology
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• 제8권3호
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• pp.64-76
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• 1980

Fig. 8 summarizes the present status of high yield pulp production and the directions of research on modification. A thick line indicates pulping process presently in use. As mentioned previously, one kind of modification is to introduce hydrophilic groups onto the pulp. Still unsolved is whether or not the introduction of hydrophilic groups should be restricted to lignin only. Goring (28) reported that middle lamella lignin has fewer phenolic hydroxyl groups than cell wall lignin and suggested that such a difference in the lignin may be useful in the removal of middle lamella lignin. The introduction of hydrophilic groups onto pulp may not be enough to modify high yield pulp. The removal of some portion of carbohydrate may be also necessary from the standpoint of softening of pulp fibers. There is no information at what lignin and carbohydrate, and how much should be removed. The combination with synthetic high polymers may also be important in modifying high yield pulp. Prof. C. Schuerch of the State University of New York who was a visiting professor at the University of Tokyo in 1974, mentioned that the hydrophilicity of lignin would be promoted, if phenolic hydroxyl or carboxyl groups could be introduced into the aromatic nucleus of lignin. If this were possible. this process would also mean a pulp yield of more than 100%. This idea is just one example of the expectation made possible through lignin chemistry. Instead of the introduction of hydrophilic group, the oxidative degradation of aromatic nucleus of lignin may also be useful in promoting the hydrophilicity of pulp. In this case, ozone may be an excellent chemical. However, there are a lot of problems to be solved such as homogeneity of reaction and selectivity of ozone for lignin. The above ideas are summarized in Fig. 9. There are many problems to be solved in the production of an excellent high yield pulp which is comparable to chemical pulp. The information from wood chemistry hopefully will elucidate some of the problems mentioned above.

• 한국공간정보시스템학회 논문지
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• 제12권1호
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• pp.37-48
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• 2010

본 논문에서는 그리드 분할과 매핑함수에 기반하여 영역질의 성능향상을 위해서 기존에 제시된 디클러스터링 방법들을 다차원 공간에 대해서 적용할 때의 문제점을 분석하고 해결법을 제시한다. 다차원 공간에 대해서 기존에 제시된 방법들을 적용할 때의 문제점은 각 차원의 분할 횟수가 적고(대부분 이진 분할이 발생함) 극히 작은 선택률에 대해서도 영역질의 각 차원의 길이가 커지기 때문에 발생한다. 본 논문에서는 이를 해결하기 위하여 다차원 공간의 다양한 그리드 분할방법에 대해서 수학적으로 성능을 예측하는 모델을 제시한다. 제시한 수학 모델을 이용하여 가능한 다양한 그리드 분할 방법들 가운데 영역질의와 겹치는 그리드 셀의 수를 감소시키는 분할 방법을 선택할 수 있으며, 이는 디클러스터링 알고리즘의 전체 성능향상으로 귀결된다. 다양한 실험결과, 본 논문에서 제시한 분할 방법을 적용할 때, 기존에 제시된 디클러스터링 알고리즘의 성능을 최대 2.7배까지 향상시킬 수 있음을 알 수 있었다.

• 대한미생물학회지
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• 제35권2호
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• pp.117-127
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• 2000

The non-ELR-containing CXC chemokines Mig and IP-10 have been shown to function as chemotactic cytokines for activated T lymphocytes. In this study, we examined the potential involvement of Mig and IP-10 in antimycobacterial response of mice immunized or infected with M. bovis BCG. The accumulation of Mig and IP-10 mRNA in resident peritoneal monocytes ($RPM{\Phi}$) was slightly reduced by stimulation with vBCG, and the degree was greater for 24 hr culture even though IFN-${\gamma}$ was added. Expression of Mig, IP-10, and IFN-${\gamma}$ in 24 hr delayed-type hypersensitivity (DTH) response was stronger in vBCG-immune mice than in the non-immune. The increase of DTH measured by foot-pad thickness appears to be clearly related to the levels of chemokines Mig and IP10 messages and those of IFN-${\gamma}$ and IL-12. Stimulation with vBCG for 2 days decreased or completely dropped the levels of Mig message in non-immune or immune splenocytes, respectively, whereas IP-10 message was slightly decreased in 2 days culture. Moreover, messages for IL-12 (p40) showed similar kinetics for Mig. The levels of Mig and IP-10 mRNA during the course of infection with BCG were not readily changed in lungs, livers, and spleens from BCG-infected mice. Although there was no obvious changes of Mig and IP-10 messages in the target organs during infection process, we found that the infection progressed over the first 3 wk before being contained by the emerging immune response suggested from detectable amount of IFN-${\gamma}$ mRNA around this time. In view of selectivity of chemokines Mig and IP-10 for activated T cells, these data suggest that chemokine Mig and IP-10, especially in collaboration with IL-12 and IFN-${\gamma}$, may playa role as T cell recruiters in immune response against mycobacterial infection.

• Biomolecules & Therapeutics
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• 제16권4호
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• pp.336-342
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• 2008

The resveratrol analogue piceatannol (3,5,3',4'-tetrahydroxy-trans-stilbene) is a polyphenol present in grapes and wine and reported to have anti-carcinogenic activities. To investigate the mechanism of anticarcinogenic activities of piceatannol, the effects on CYP 1 enzymes were determined in Escherichia coli membranes coexpressing recombinant human CYP1A1, CYP1A2 or CYP1B1 with human NADPH-P450 reductase. Piceatannol showed a strong inhibition of CYP1A1 and CYP1B1 in a concentration-dependent manner, and $IC_{50}$ of human CYP1A1 and CYP1B1 was 5.8 ${\mu}M$ and 16.6 ${\mu}M$, respectively. However, piceatannol did not inhibit CYP1A2 activity in the concentration of up to 100 ${\mu}M$. Piceatannol exhibited 3-fold selectivity for CYP1B1 over CYP1A1. The mode of inhibition of piceatannol was non-competitive for CYP1A1 and CYP1B1. The result that piceatannol did not inhibit CYP1B1-mediated $\alpha$-naphthoflavone ($\alpha$-NF) metabolism suggests piceatannol may act as a non-competitive inhibitor as well. In human prostate carcinoma PC-3 cells, piceatannol induces apoptosis and prevents Aktmediated signal pathway. Taken together, abilities of piceatannol to induce apoptotic cell death as well as CYP1 enzyme inhibition make this compound a useful tool for cancer chemoprevention.

• KSBB Journal
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• 제20권2호
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• pp.88-92
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• 2005

인산화 과정은 serine, threonine, tyrosine에서 발생하는 생화학적 반응으로, 본 연구에서는 다양한 응용의 잠재능력이 있는 phosphoserine, phosphothreonine, phosphotyrosine에 대한 엡타머를 개발하였다. 우선 in vitro selection 방법에 의해 combinatorial chemistry로부터 얻어진 RNA library로부터 이들 phosphoamino acids와 친화도를 가지고 있는 엡타머를 찾아낼 수 있었다. 총 10번의 일련 과정을 통해 phosphoserine에 대해서 2.6 nM의 친화도를 가지고 있는 엡타머를 (SeA-06), phosphothreonine에 대해서는 2.7nM의 친화도를 가지고 있는 엡타머 (TrA-18)를 찾아낼 수 있었고, 이들의 RNA 2차 구조를 각각 예측하여 보았다. 그러나 phosphotyrosine의 경우 짧은 길이의 엡타머가 selection됨으로 내부적으로 구조를 가지는 엡타머는 얻을 수 없었다. o-phosphoserine에 대한 항체가 기존에 보고가 되었으나 유사한 구조를 지닌 o-phosphothreonine에도 비슷한 활성을 보여 이들을 구분할 수 있는 리간드를 찾기 힘들었으나, 본 연구에서는 엡타머를 사용한 특이성 조사에서도 서로를 극명하게 구별할 수 있음을 확인할 수 있었다. 이와 같이 발굴된 엡타머를 사용하여 biochip이나 Proteomics 분석 도구의 응용에 큰 기대효과를 제공할 수 있을 것이라 사료된다.