• 제목/요약/키워드: subunits$(\alpha'-,\

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Cooperativity of ${\alpha}$- and ${\beta}$-Subunits of Group II Chaperonin from the Hyperthermophilic Archaeum Aeropyrum pernix K1

  • Kim, Jeong-Hwan;Lee, Jin-Woo;Shin, Eun-Jung;Nam, Soo-Wan
    • Journal of Microbiology and Biotechnology
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    • 제21권2호
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    • pp.212-217
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    • 2011
  • ${\alpha}$ and ${\beta}$-subunits (ApCpnA and ApCpnB) are group II chaperonins from the hyperthermophilic archaeum Aeropyrum pernix K1, specialized in preventing the aggregation and inactivation of substrate proteins under conditions of transient heat stress. In the present study, the cooperativity of ${\alpha}$- and ${\beta}$-subunits from the A. pernix K1 was investigated. The ApCpnA and ApCpnB chaperonin genes were overexpressed in E. coli Rosetta and Codonplus (DE3), respectively. Each of the recombinant ${\alpha}$- and ${\beta}$-subunits was purified to 92% and 94% by using anionexchange chromatography. The cooperative activity between purified ${\alpha}$- and ${\beta}$-subunits was examined using citrate synthase (CS), alcohol dehydrogenase (ADH), and malate dehydrogenase (MDH) as substrate proteins. The addition of both ${\alpha}$- and ${\beta}$-subunits could effectively protect CS and ADH from thermal aggregation and inactivation at $43^{\circ}C$ and $50^{\circ}C$, respectively, and MDH from thermal inactivation at $80^{\circ}C$C and $85^{\circ}C$. Moreover, in the presence of ATP, the protective effects of ${\alpha}$- and ${\beta}$-subunits on CS from thermal aggregation and inactivation, and ADH from thermal aggregation, were more enhanced, whereas cooperation between chaperonins and ATP in protection activity on ADH and MDH (at $85^{\circ}C$) from thermal inactivation was not observed. Specifically, the presence of both ${\alpha}$- and ${\beta}$- subunits could effectively protect MDH from thermal inactivation at $80^{\circ}C$ in an ATP-dependent manner.

Coordinated Spatial and Temporal Expression of Voltage-sensitive calcium Channel ${\alpha}_{1A}$ and $\beta_4$ Subunit mRNAs in Rat Cerebellum

  • Kim, Dong-Sun;Chin, Hemin
    • Animal cells and systems
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    • 제1권4호
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    • pp.589-594
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    • 1997
  • The neuronal voltage-sensitive calcium channels (VSCCs) are multisubunit complexes consisting of $\alpha_1,\;\alpha_2-\delta$ and $\beta$ subunits. Heterologous expression and biochemical studies have shown that the activity of VSCCs is regulated by their $\beta$ subunits in a $\beta$ subunit isoform-specific manner. To elucidate the $\beta$ subunit identity of the P/Q-type calcium channel encoded by an $\alpha_{1A}$ subunit, which is exclusively expressed in the Purkinje and granule cell of the cerebellum, we have examined the spatial and temporal expression patterns of $\beta$ subunits and compared them with those of $\alpha_{1A}$ subunit in the developing rat cerebellum. Reverse transcriptase- polymerase chain reaction (RT-PCR) and Northern blot analysis have shown that $\beta_4$ subunit mRNA was prominently expressed in the cerebellum and much more abundant than any other distinct $\beta$ subunits. RNase protection assay has further demonstrated that the expression of $\alpha_{1A}$ and $\beta_4$ subunits increased during cerebellar development, while the amount of $\beta_2$ and $\beta_3$ mRNAs did not significantly change. In addition, a $\beta_4$ transcript was present in cultured cerebellar granule cells, but not in astrocyte cells, and the level of $\beta_4$ mRNA expression increased gradually in vitro seen as in vivo. Based on the spatial and temporal expression patterns of $\beta_4$ subunit, we conclude that $\beta_4$ may predominantly associate, but probably not exclusively, with the $\alpha_{1A}$ subunit in rat cerebellar granule cells.

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콩 종실 단백질의 유전변이 (Genetic variation of 7S and 11S globulins in soybean seed)

    • 한국자원식물학회지
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    • 제12권3호
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    • pp.198-203
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    • 1999
  • 콩 저장 단백질의 대부분은 globulin이며, 이중 7S와 11S가 70% 이상을 차지한다. 따라서 콩 단백질의 조성개량을 위해서는 11S/7S비율 조정이 우선되는데, 본 연구에서는 전기영동(SDS-PAGE)법을 사용하여 콩 단백질 7S와 11S를 분리 확인하고, 이들 분획 단백질의 유전변이를 분석하였다. 국내 3개지역에서 재배된 콩 장려품종 6계통들의 평균 7S 함량은 38.9% 이었고 11S는 61.2%의 함량을 나타내었다. 분산분석 결과 품종간에 는 유의성이 있었지만 지역간에는 변이가 없었으며, 품종 x 지역의 상호작용은 고도의 유의성을 나타내었다. 유전력은 7S분획중의 $\beta$함량이 72.7%로 높게 나타났다. 공분산을 이용한 상관계수 추정에서는 유전상관이 표현형 상관 보다 다소 높게 나타났다. 따라서 7S와 11S의 분획간 함량을 조정함으로써 콩 단백질의 조성을 개량할 수 있으리라 판단된다.

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Recombinant α and β Subunits of M.AquI Constitute an Active DNA Methyltransferase

  • Pinarbasi, Hatice;Pinarbasi, Ergun;Hornby, David
    • BMB Reports
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    • 제35권3호
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    • pp.348-351
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    • 2002
  • AquI DNA methyltransferase, M.AquI, catalyses the transfer of a methyl group from S-adenosyl-L-methionine to the C5 position of the outermost deoxycytidine base in the DNA sequence 5'CYCGRG3'. M.AquI is encoded by two overlapping ORFs (termed $\alpha$ and $\beta$) instead of the single ORF that is customary for Class II methyltransferase genes. The structural organization of the M.AquI protein sequence is quite similar to that of other bacterial C5-DNA methyltransferases. Ten conserved motifs are also present in the correct order, but only on two polypeptides. We separately subcloned the genes that encode the $\alpha$ and $\beta$ subunits of M.AquI into expression vectors. The overexpressed His-fusion $\alpha$ and $\beta$ subunits of the enzyme were purified to homogeneity in a single step by Nickel-chelate affinity chromatography. The purified recombinant proteins were assayed for biological activity by an in vitro DNA tritium transfer assay. The $\alpha$ and $\beta$ subunits of M.AquI alone have no DNA methyltransferase activity, but when both subunits are included in the assay, an active enzyme that catalyses the transfer of the methyl group from S-adenosyl-L-methionine to DNA is reconstituted. We also showed that the $\beta$ subunit alone contains all of the information that is required to generate recognition of specific DNA duplexes in the absence of the $\alpha$ subunit.

전위활성화 칼슘이온통로의 구조, 기능 및 조절

  • 이정하
    • 한국동물학회:뉴스레터
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    • 제18권2호
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    • pp.38-44
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    • 2001
  • 전위활성화 칼슘통로를 통한 칼슘이온의 세포 내 유입은 근육수축, 시냅스 전달, 호르몬 분비, 효소의 활성도 및 유전자 발현을 조절한다. 이와 같이 중요한 생리적 기능을 조절하기 때문에 칼슘통로를 대상으로 한 다방면의 연구가 과거 20년간 활발히 진행되어 왔다 칼슘통로는 $\alpha$1, $\alpha$2-$\delta$, $\beta$로 구성되어 있으며, 이 중 $\alpha$1은 칼슘통로의 일반적 특성을 나타내는 기본 구조체이며, $\alpha$2-$\delta$$\beta$$\alpha$1을 조절하는 보조 기능을 한다. 지금까지 10개의 $\alpha$1 subunits(L-형: $\alpha$1S, $\alpha$1C, $\alpha$1D, $\alpha$1F; non-L-형: $\alpha$1A, a1B, $\alpha$1E; T-형: $\alpha$1G, $\alpha$1H, $\alpha$1I), 4종류의 $\beta$ subunits, 3 종류의 $\alpha$2-$\delta$ subunits가 클로닝되었으며, 이들 클론을 이용한 분자 수준에서의 연구가 활발히 이루어지고 있다. 본 논단에서는 칼슘통로의 구조, 기능 및 조절에 대한 연구가 전기생리학적, 분자생물학적 및 약리학적 방법을 사용하여 어떻게 수행되어왔는지 살펴보고, 최근 연구성과에 대해서도 소개하고자 한다.

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Possible target for G protein antagonist: Identification of specific amino acid residue responsible for the molecular interaction of G$\alpha$ 16 with chemoattractant C5a receptor.

  • 이창호
    • 한국응용약물학회:학술대회논문집
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    • 한국응용약물학회 2000년도 춘계학술대회
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    • pp.17-19
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    • 2000
  • Heterotrimeric G Proteins transduce ligand binding to a wide variety of seven transmembrane cell surface receptors into intracellular signals. The currently accepted model for the activation of G protein suggests that ligand-activated receptor accelerates GDP-GTP exchange reactions on the ${\alpha}$ subunit of the heterotrimeric G protein. At least seventeen distinct isoforms of the G${\alpha}$ subunit protein have been identified in mammalian organisms. Among them, the G${\alpha}$q family consists of five members whose ${\alpha}$ subunits show different expression patterns. G${\alpha}$q and G${\alpha}$11 seem to be almost ubiquitously expressed, whereas G${\alpha}$14 is predominantly expressed in spleen, lung, kidney and testis. G${\alpha}$16 and its murine counterpart G${\alpha}$15 are expressed in hematopoietic cells and has been shown to couple a wide variety of receptors to phosphoinositide-specific phospholipase C activity. Beta-isoforms of phospholipase C were shown to be activated by all members of G${\alpha}$q family, i.e., G${\alpha}$q, G${\alpha}$11, G${\alpha}$l4 and G${\alpha}$16 subunits either in reconstitution system. or in experiments using cDNA transfection with intact Cos-7 cells.

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말 태반과 뇌하수체에서 당단백질 호르몬의 특이적인 발현 (Differential Expression of Glycoprotein Hormones in Equine Placenta and Pituitary)

  • Min, Kwan-Sik
    • 한국발생생물학회지:발생과생식
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    • 제4권1호
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    • pp.87-93
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    • 2000
  • eCG는LH, FSH및 TSH와 같이 당단백질 호르몬에 속하고, 당쇄가 많이 첨가된 $\alpha$$\beta$-subunits의 비공유결합으로 구성되어 있고, 말에서 보다 다른 동물에서 FSH와 LH의 이중 생리활성을 나타내는 아주 특이한 성선 자극 호르몬이다. eCG는 임신 40~130일 사이에 말의 자궁내막배의 영양막세포에서 합성ㆍ분비된다. 따라서 본 연구에서는 eCG, eLH 및 eFSH의 각각 subunits mRNA발현을 태반과 뇌하수체에서 분석하였다. mRNA의 추출은 임신 70일의 태반과 27개월된 숫컷말의 뇌하수체에서 분리하였다. 말 태반을 이용한eCG mRNA발현의 Northern blotting분석결과 $\beta$ subunit가 $\alpha$ subunit보다 아주 많이 발현되었으며, 또한 뇌하수체에서 $\alpha$-, LH $\beta$-, FSH $\beta$-subunit의 분석결과 $\alpha$ subunit는 약 0.8 kb, FSH $\beta$ subunit는 1.8 kb의 크기로 발현되었는데, 이러한 FSH $\beta$ subunit는 cloning되어진 cDNA의 크기와 일치한다. 뇌하수체 전엽에서는 $\alpha$ subunit가 LH $\beta$ subunit와 FSH $\beta$ subunit보다 현저히 많이 발현된다는 사실이 밝혀졌다. 따라서, 태반과 뇌하수체에서 발현되는 각각 subunit의 mRNA는 독립적으로 조절되어 결과적으로 발현량에 차이가 나타난다고 시사되어진다.

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Capsaicin, a component of red peppers, stimulates protein kinase CKII activity

  • Rho, Yun-Wha;Bae, Young-Seuk
    • BMB Reports
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    • 제43권5호
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    • pp.325-329
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    • 2010
  • Protein kinase CKII (CKII), a heterotetramer composed of two catalytic ($\alpha$ or $\alpha$') subunits and two regulatory ($\beta$) subunits, plays a critical role in cell proliferation and anti-apoptosis. Recently, capsaicin was shown to trigger apoptosis. Therefore, we examined the effect of capsaicin on CKII activity. Although capsaicin induced apoptotic death in HeLa cells, CKII activity was increased in the cytosolic fraction of HeLa cells after treatment. Capsaicin did not change the expression of the $CKII{\alpha}$ and $CKII{\beta}$ proteins. Capsaicin stimulated the catalytic activity of recombinant CKII tetramer, but not the $CKII{\alpha}$ subunit. Moreover, capsaicin enhanced the autophosphorylation of $CKII{\alpha}$ and $CKII{\beta}$. Taken together, our data suggest that capsaicin stimulates the phosphotransferase activity of CKII holoenzyme by interacting with the $CKII{\beta}$ subunit.

24번 잔기가 치환된 트립토판 중합효소 $\alpha$ 소단위체들의 구조풀림 성질 (Unfolding Property of Residue 24-Substituted Tryptophan Synthase $\alpha$-Subunits)

  • 정지은;박후휘;신혜자;임운기
    • 생명과학회지
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    • 제9권6호
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    • pp.733-736
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    • 1999
  • 대장균 트립토판 중합요소 (tryptophan synthase) $\alpha$ 소단위체의 24번 잔기인 트레오닌이 메티오닌, 알라닌 또는 세린으로 치환되고 잔기 139에 트립토판이 있는 단백질를 정제하여, 여러가지 요소 농도에 대한 트립토판 형광값의 변화를 측정하여 변성곡선을 얻었다. 이들 단백질들은 모두 F139W 단백질에 비해 구조형성 성질에 큰 변화를 일으켰으며, 잔기 24번은 구조형성에 중요한 것으로 추정된다.

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Cloning and Characterization of the psbEF Gene Encoding Cytochrome b-559 of the Panax ginseng Photosystem II Reaction Center

  • Lee, Won-Kyu;Park, Dae-Sung;Tae, Gun-Sik
    • BMB Reports
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    • 제32권2호
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    • pp.189-195
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    • 1999
  • From the Panax ginseng chloroplast, the psbE and psbF genes, encoding the $\alpha$- and $\beta$-subunits of cytochrome b-559 of the photosystem II reaction center, respectively, were cloned and characterized. The psbE and psbF genes were composed of 252 and 117 nucleotides, respectively. The deduced amino acid sequence of the $\alpha$-subunits showed 95%, 93%, and 91% homology to monocots, dicots, and liverwort, respectively, whereas the $\beta$-subunits showed approximately 98% to 95% homology to the same species. Southern blot analysis revealed that a single copy of the psbEF gene exists in the chloroplast plastid. Northern blot analysis indicated that the psbE and psbF genes are cotranscribed as a polycistron.

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