• Korean Journal of Mathematics
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• 제23권1호
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• pp.153-161
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• 2015

In this work, we consider an elliptic system $$\left{\array {-{\Delta}u=au+bv+{\delta}_1u+-{\delta}_2u^-+f_1(x,u,v) && in\;{\Omega},\\-{\Delta}v=bu+cv+{\eta}_1v^+-{\eta}_2v^-+f_2(x,u,v) && in\;{\Omega},\\{\hfill{70}}u=v=0{\hfill{90}}on\;{\partial}{\Omega},}$$, where ${\Omega}{\subset}R^N$ be a bounded domain with smooth boundary. We prove that the system has at least two nontrivial solutions by applying linking theorem.

• Journal of Magnetics
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• 제5권4호
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• pp.116-119
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• 2000

Magnetic field dependence of magnetization reversal in Co/Pt multilayers was quantitatively investigated. Serial samples of Co/Pt multilayers were prepared by dc-magnetron sputtering under various Ar pressures. Magnetization reversal was monitored by magnetization viscosity measurement and direct domain observation using a magneto-optical microscope system, and the wall-motion speed V and the nucleation rate R were determined using a domain reversal model based on time-resolved domain reversal patterns. Both V and R were found to be exponentially dependent on the applied reversing field. From the exponential dependencies, the activation volumes for wall motion and nucleation could be determined, based on a thermally activated relaxation model, and the wall-motion activation volume was found to be slightly larger than the nucleation activation volume.

• Fisheries and Aquatic Sciences
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• 제26권9호
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• pp.558-568
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• 2023

Vibrio vulnificus is an aquatic bacterium causing septicemia and wound infection in humans. To understand this pathogen at the genomic level, it was performed whole genome sequencing of a cefoxitin-resistant strain, V. vulnificus 1908-10 possessing virulence-related genes (vvhA, viuB, and vcgC) isolated from Gadeok island coastal seawater in South Korea. The genome of V. vulnificus 1908-10 consisted of two circular contigs and no plasmid. The total genome size was estimated to be 5,018,425 bp with a guanine-cytosine (GC) content of 46.9%. We found 119 tRNA and 34 rRNA genes respectively in the genome, along with 4,352 predicted protein sequences. Virulence factor (VF) analysis further revealed that V. vulnificus 1908-10 possess various virulence genes in classes of adherence, antiphagocytosis, chemotaxis and motility, iron uptake, quorum sensing, secretion system, and toxin. In the comparison of the presence/absence of virulence genes, V. vulnificus 1908-10 had fur, hlyU, luxS, ompU, pilA, pilF, rtxA, rtxC, and vvhA. Of the 30 V. vulnificus comparative strains, 80% of the C-genotype strains have all of these genes, whereas 40% of the E-genotype strains have all of them. In particular, pilA were identified in 80% of the C-type strains and 40% of the E-type strains, showing more difference than other genes. Therefore, V. vulnificus 1908-10 had similar VF characteristics to those of type C strains. Multifunctional-autoprocessing repeats-in-toxin (MARTX) toxin of V. vulnificus 1908-10 contained 8 A-type repeats (GXXGXXXXXG), 25 B.1-type repeats (TXVGXGXX), 18 B2-type repeats (GGXGXDXXX), and 7 C-type repeats (GGXGXDXXX). The National Center for Biotechnology Information (NCBI) Basic Local Alignment Search Tool (BLAST) showed that the RtxA protein of V. vulnificus 1908-10 had the effector domain in the order of cross-liking domain (ACD)-C58_PaToxP-like domain- α/β hydrolase-C58_PaToxP-like domain.

• 대한수학회보
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• 제54권6호
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• pp.1969-1980
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• 2017

Let ${\Gamma}$ be a nonzero torsionless commutative cancellative monoid with quotient group ${\langle}{\Gamma}{\rangle}$, $R={\bigoplus}_{{\alpha}{\in}{\Gamma}}R_{\alpha}$ be a graded integral domain graded by ${\Gamma}$ such that $R_{{\alpha}}{\neq}\{0\}$ for all ${\alpha}{\in}{\Gamma},H$ be the set of nonzero homogeneous elements of R, C(f) be the ideal of R generated by the homogeneous components of $f{\in}R$, and $N(H)=\{f{\in}R{\mid}C(f)_v=R\}$. In this paper, we introduce the notion of graded t-almost Dedekind domains. We then show that R is a t-almost Dedekind domain if and only if R is a graded t-almost Dedekind domain and RH is a t-almost Dedekind domains. We also show that if $R=D[{\Gamma}]$ is the monoid domain of ${\Gamma}$ over an integral domain D, then R is a graded t-almost Dedekind domain if and only if D and ${\Gamma}$ are t-almost Dedekind, if and only if $R_{N(H)}$ is an almost Dedekind domain. In particular, if ${\langle}{\Gamma}{\rangle}$ isatisfies the ascending chain condition on its cyclic subgroups, then $R=D[{\Gamma}]$ is a t-almost Dedekind domain if and only if R is a graded t-almost Dedekind domain.

• 한국정보통신학회:학술대회논문집
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• 한국해양정보통신학회 2010년도 춘계학술대회
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• pp.483-485
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• 2010

Rail-to-rail 입력 범위를 가지는 200kS/s 10-bit successive approximation (SA) ADC가 제안된다. 제안된 SA ADC는 DAC, 비교기, 그리고 successive approximation register (SAR) logic으로 구성된다. DAC는 전력소모를 줄이고 면적을 줄이기 위해 capacitor를 이용한 folded-type으로 구현되며, parasitic 성분에 의한 영향을 줄이기 위해 boosted NMOS switch를 사용한다. 또한 fully differential voltage-to-time converter를 이용하는 time-domain comparator를 제안한다. 이는 PSRR 및 CMRR을 향상시킨다. 또한 출력의 유효구간을 반으로 줄인 flip-flop을 사용함으로 SAR logic의 전력소모와 chip area를 줄인다. 제안된 SA ADC는 1V supply를 가지는 $0.18{\mu}m$ CMOS 공정을 사용한다.

• BMB Reports
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• 제56권11호
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• pp.606-611
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• 2023

The main protease (Mpro) of SARS-CoV-2 cleaves 11 sites of viral polypeptide chains and generates essential non-structural proteins for viral replication. Mpro is an important drug target against COVID-19. In this study, we developed a real-time fluorometric turn-on assay system to evaluate Mpro proteolytic activity for a substrate peptide between NSP4 and NSP5. It produced reproducible and reliable results suitable for HTS inhibitor assays. Thus far, most inhibitors against Mpro target the active site for substrate binding. Mpro exists as a dimer, which is essential for its activity. We investigated the potential of the Mpro dimer interface to act as a drug target. The dimer interface is formed of domain II and domain III of each protomer, in which N-terminal ten amino acids of the domain I are bound in the middle as a sandwich. The N-terminal part provides approximately 39% of the dimer interface between two protomers. In the real-time fluorometric turn-on assay system, peptides of the N-terminal ten amino acids, N10, can inhibit the Mpro activity. The dimer interface could be a prospective drug target against Mpro. The N-terminal sequence can help develop a potential inhibitor.

• 한국전자파학회논문지
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• 제24권3호
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• pp.310-315
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• 2013

본 논문에서는 전력 케이블의 전파상수를 추출하는 2-port time-domain reflectometry(TDR) 방법을 제안한다. 케이블을 투과하는 펄스 신호를 시간 영역에서 측정하고 주파수 영역에서 분석하여 전파상수를 추출하였다. 22.9 kV 325 $mm^2$ XLPE 케이블의 전파상수를 2.14 GHz까지 추출하고 network analyzer 로 측정한 케이블의 $S_{21}$을 비교하여 2-port TDR 방법의 타당성을 입증하였다. 그 결과, 기존의 TDR 방법보다 측정 가능한 상한 주파수가 증가하고, 고주파수에서 오차가 줄어드는 것을 확인하였다.

• 한국결정성장학회지
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• 제16권2호
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• pp.53-58
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• 2006

조화용융조성 $LiNbO_3$ 결정에 외부 전계를 인가하였을 때 초기 도메인 생성 및 이동에 관하여 연구하였다. 0.5mm 두께의 $LiNbO_3$ 결정에 23.5, 22.0, 21.0kV/mm의 전계를 인가하였을 때 도메인 벽은 각각 28.70, 16.02, $5.75{\mu}m/sec$의 속도를 나타내었다. 분극 반전 시스템에 전류 제어를 위한 외부저항으로 $1 M{\Omega}$을 사용하였을 시 너무 빠른 도메인 성장으로 인하여 원활한 분극 반전 제어가 이루어지지 않으므로 $10 M{\Omega}$ 외부저항을 사용하여 전하량을 제어하여 50% duty cycle을 가진 주기적 분극 반전 $LiNbO_3$ 결정을 제작하였다.

• 한국세라믹학회지
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• 제33권2호
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• pp.228-234
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• 1996

강유전성 BaTiO3의 분역 구조를 이해하는 것은 폴링과정에 있어서 대단히 중요하면 대부분의 BaTiO3 세라믹스에서 흔히 발견되는 구조 쌍정 계면에서의 배향관계는 아직까지 보고된 바 없다. 본 연구에서는 {111} 쌍정을 이루고 있는 길정시편을 이용하여 편광현미경하에서 분역구조를 관찰하고, 열처리에 의하여 상전이되는 동안 {111} 쌍정과 강유전성 분역의 거동을 현미경하에서 직접적으로 관찰하였다. {111} 쌍정면 암측으로 대칭적 분역구조가 발될되며, 그 배열 형태는 'V'자 모양과 수직하게 관통하는 것처럼 직선 모양의 두가지 형으로 분류된다. 열처리에 의하여 새로운 분역구조가 형성될때 {111} 쌍정면 주위에서는 대칭적 관계를 유지하면서 분역이 발달되며, 분역형성에 기인하는 표면변형도 {111} 쌍정에 대하여 항상 대칭적으로 발달된다. 이는 {111} 계면에서도 분극반향이 바뀌어지며 "머리-꼬리"의 전지적 안정성의 배향관계를 유지하는 것으로 설명할 수 있다.

• Bulletin of the Korean Chemical Society
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• 제34권12호
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• pp.3665-3670
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• 2013

The R3V6 peptide includes a hydrophilic arginine stretch and a hydrophobic valine stretch. In previous studies, the R3V6 peptide was evaluated as a gene carrier and was found to have low cytotoxicity. However, the transfection efficiency of R3V6 was lower than that of poly-L-lysine (PLL) in N2A neuroblastoma cells. In this study, the transfection efficiency of R3V6 was improved in combination with high mobility group box 1A domain (HMGA). HMGA is originated from the nuclear protein and has many positively-charged amino acids. Therefore, HMGA binds to DNA via charge interaction. In addition, HMGA has a nuclear localization signal peptide and may increase the delivery efficiency of DNA into the nucleus. The ternary complex with HMGA, R3V6, and DNA was prepared and evaluated as a gene carrier. First, the HMGA/DNA complex was prepared with a negative surface charge. Then, R3V6 was added to the complex to coat the negative charges of the HMGA/DNA complex, forming the ternary complex of HMGA, R3V6, and DNA. A physical characterization study showed that the ternary complex was more stable than the PLL/DNA complex. The HMGA/R3V6/DNA complex had a higher transfection efficiency than the PLL/DNA, HMGA/DNA, or R3V6/DNA complexes in N2A cells. Furthermore, the HMGA/R3V6/DNA complex was not toxic to cells. Therefore, the HMGA/R3V6/DNA complex may be a useful gene delivery carrier.