• 한국가축번식학회지
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• 제25권1호
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• pp.63-69
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• 2001

본 연구는 돼지 미성숙 난포란을 체외에서 성숙, 수정시킨 후, 체외배양액내에 NO Scavenger인 hemoglobin과 억제제인 L-NAME의 첨가 배양이 돼지 체외수정란의 체외발육에 미치는 효과를 검토하였다. 체외배양 44시간에 NCSU 배양액에 hemoglobin을 각각 0, 1 및 5$\mu\textrm{g}$/$m\ell$가 첨가된 처리구에서 상실배기 이상 발육된 수정란의 체외 발육율은 각각 52.4%, 57.6% 및 57.4%로써 hemoglobin 첨가군이 대조군에 비해 다소 높은 발육성적을 나타냈으나 통계적 유의성은 인정되지 않았다 (P〉0.05). 체외배양 96시간에 NCSU23 배양액에 hemoglobin을 0, 1 및 5$\mu\textrm{g}$/$m\ell$ 첨가한 처리구에서 상실배이상 발육된 체외 발육성적은 각각 66.2%, 70.8% 및 62.8%로 1$\mu\textrm{g}$/$m\ell$ hemoglobin을 첨가한 처리구가 다른 처리구보다 다소 높게 나타났지만 통계적으로 유의차는 인정되지 않았다 (P〉0.05). 체외배양 44시간에 NCSU23 배양액에 L-NAME를 각각 0, 10, 50 및 100mM을 첨가한 처리구에서 상실배기 이상 발육된 체외발육율은 각각 65.2%, 73.5%, 70.1% 및 58.8%로 L-NAME를 10mM첨가한 처리구와 50mM 첨가한 구가 무 첨가구와 100mM 첨가구보다 통계적으로 유의하게 높은 성적을 얻었다 (P＜0.05). 각 처리구에서 생산된 배반포기수정란의 세포수에는 커다란 차이가 인정되지 않았다.

• Bulletin of the Korean Chemical Society
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• 제23권8호
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• pp.1073-1077
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• 2002

Binding of dodecyl trimethylammonium bromide (DTAB) to human and bovine hemoglobin and globin samples has been investigated in 50 mM glycine buffer pH = 10, I = 0.0318 and 300 K by equilibrium dialysis and temperature scanning spectrophotometry techniques and method for calculation of average hydrophobicity. The binding data has been analyzed, in terms of binding capacity concept $({\theta})$, Hill coefficient (nH) and intrinsic Gibbs free energy of binding $({\Delta}Gbv).$ The results of binding data, melting point (Tm) and average hydrophobicity show that human hemoglobin has more structural stability than bovine hemoglobin sample. Moreover the results of binding data analysis represent the systems with two and one sets of binding sites for hemoglobin and globin, respectively. It seems that the destabilization of hemoglobin structure due to removal of heme group, is responsible of such behavior. The results indicating the removal of heme group from hemoglobin caused the depletion of first binding set as an electrostatic site upon interaction with DTAB and exposing the hydrophobic patches for protein.

• BMB Reports
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• 제35권4호
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• pp.364-370
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• 2002

The effect of sodium n-dodecyl sulphate (SDS) on hemoglobin autoxidation was studied in the presence of a 100mM phosphate buffer (pH 7.0) by different methods. These included spectorphotometry, fluorescence technique, cyclic voltametry, differential scanning calorimetry, and densitometry. Spectroscopic studies showed that SDS concentrations up to 1 mM increased deoxy-, decreases oxy-, and had no significant effect on the met- conformation of hemoglobin. Therefore, a SDS concentration up to 1 mM increased the deoxy form of hemoglobin as the folded, compact state and decreases the oxy conformation. The turbidity measurements and differential scanning calorimetry techniques indicated a more stable conformation for hemoglobin in the presence of SDS up to 1mM. Electrochemical studies also confirmed a more difficult oxidation under these conditions. The induction of the deoxy form in the presence of SDS was confirmed by densitometry techniques. The compact structure of deoxyhemoglobin blocks the formation of met-conformation in low SDS concentrations.

• BMB Reports
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• 제29권3호
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• pp.261-265
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• 1996

Sheep hemoglobin (SHb) was modified with methoxy-polyethylene glycol (mPEG) to develop a potential blood substitute. mPEG has been used to decrease antigenicity and immunogenicity of foreign proteins. When the mPEG was attached to SHb, the modified hemoglobins showed decreased electrophoretic mobility on SDS-PAGE and decreased free amino groups. When the remaining free amino groups of mPEG modified SHb were determined by TNBS free amino group titration methods. about 34% of total free amino groups were modified with mPEG. This mPEG-SHb conjugate of 34% amino groups modified showed no precipitation by double immunodiffusion with polyclonal antibodies against SHb. This modified hemoglobin still has oxygen transport activity. So this antigenicity decreased hemoglobin may be used in humans as a potential blood substitute.

• 분석과학
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• 제36권6호
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• pp.332-339
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• 2023

Urea는 혈액의 hemoglobin을 변성시켜 효소 활성 자리를 노출시킴으로써 혈액-luminol 반응의 화학발광 세기를 향상시킨다는 가설을 검증하고자 하였다. 이를 위해 혈액을 urea로 전처리한 경우 urea의 농도가 더 높아지거나 전처리 시간이 늘어날수록 혈액-luminol 반응의 화학발광 세기가 증가하였고 이는 기존의 가설과 부합되는 결과였다. 하지만 8 M urea용액을 미리 혼합하여 제조한 luminol로 혈액을 처리하면 혈액을 urea로 미리 전처리한 경우에 비해 urea가 hemoglobin을 변성시키는 시간이 짧아짐에도 화학발광 세기가 오히려 증가하는 현상이 나타났다. 또한 hemoglobin이 없는 전이금속을 urea가 포함된 luminol과 반응시켰을 때 화학발광이 강해지는 현상이 관찰되었다. 이러한 점으로 미루어 볼 때 urea는 hemoglobin을 변성시킬 뿐만 아니라 luminol-hydrogen peroxide 반응에도 관여하는 것으로 예상된다.

• 한국환경보건학회지
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• 제32권2호
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• pp.164-170
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• 2006

Ethylene oxide is a genotoxic carcinogen with widespread uses as industrial chemical intermediate and gaseous sterilant. 2-hydroxyethylated N-terminal valine in Hb is a good biomarker for biological monitoring of ethylene oxide exposure, because of its stability. For measuring the hemoglobin adduct formed by exposure of ethylene oxide, we studied the determination of (N-2-hydroxy-ethyl)valine(HEV) in hemoglobin adduct by using GC/MS. Firstly we synthesized HEV with 2-amino-ethanol and bromoisovaleric acid(BIVA) and confirmed it with GC/MS-FID. Its fragmentations were m/z 116(base ion, M+-45) and m/z 130(M+-31). For measuring HEV with higher sensitivity, we use derivatives which were PFPITH(pentafluorophenylisothiocianate) and TBDMS (tributyldimethylsilylation) by using Edman procedure. Its fragmentation were m/z 425(M+-57), m/z 383(M+-99) and m/z 172(M+-310) by using GC/MS. We did biological monitoring for mice inhalation exposure with 400 ppm ethylene oxide. The concentrations of hemoglobin adduct were $168{\pm}3.8\;and\;512{\pm}04$(nmol g-1 globin) at 0.5 hr/day 400 ppm ethylene oxide inhalation exposure group, and $631{\pm}17\;and\;2265{\pm}9.4$(nmol g-1 globin) at 1.0 hr/day 400 ppm ethylene oxide inhalation exposure for 1 and 4 weeks, respectively. We confirmed that (N-2-hydroxy-ethyl)valine(HEV) of hemoglobin was a good biomarker for biomonitoring of ethylene oxide exposure, and can measured with derivatives such as PFPITH(pentafluorophenylisothiocianate) and TBDMS(tributyldimethylsilylation) by using GC/MS.

• 한국산업보건학회지
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• 제10권2호
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• pp.124-139
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• 2000

This study was performed to investigate monoacetylbenzidine(MABZ) and benzidine(BZ) hemoglobin adducts among workers who worked at benzidine based dye manufacturing company, and exposed by benzidine and benzidine based dye. The hemoglobin adducts were compared with work environment assessment result for evaluating the usefulness of biological monitoring. The mean BZ hemoglobin adducts among the first synthesis worker's hemoglobin adducts were $40.69{\mu}gBZ/g$ Hb and those of dry and packing workers were $22.14{\mu}gBZ/g$ Hb. The mean of MABZ hemoglobin adducts among 1st synthesis workers were $255.84{\mu}gMABZ/g$ Hb, dispersion worker's hemoglobin adducts were $76.17{\mu}gMABZ/g$ Hb and synthesis worker's hemoglogin adducts were $28.66{\mu}gMABZ/g$ Hb. Work environment assessment results during past 3 years were $0.0065mg/m^3$ and $0.5659mg/m^3$ of benzidine based dye concentration in ambient air of drying and packing only. Dye producing process was categorized by the possibility of exposure to benzidine and benzidine based dye. BZ and MABZ hemoglobin adducts were $19.55{\mu}gBZ/g$ Hb, $119.80{\mu}gMABZ/g$ Hb among workers who exposed by benzidine dihydrochloride and $16.32{\mu}gBZ/g$ Hb, $316.56{\mu}gMABZ/g$ Hb among workers who exposed by benzidine based dye. BZ hemoglobin adducts were not detected among control group and MABZ hemoglobin adducts were $5.33{\mu}gMABZ/g$ Hb. The differences between control and other exposed group was statistically significant. But there was no statistically significant differences between benzidine dihydrochloride exposed process and benzidine based dye exposed group. BZ and MABZ hemoglobin adducts were $2.23{\mu}gBZ/g$ Hb, $76.17{\mu}gMABZ/g$ Hb and $3.46{\mu}gBZ/g$ Hb, $21.33{\mu}gMABZ/g$ Hb. So hemoglobin adducts of MABZ were 5 ~ 30 time higher than those of BZ(P<0.003). Above results indicate that work environment assessment didn't detected benzidine and benzidine based dye in ambient air but biological monitoring detected those of hemoglobin adducts. Two group's hemoglobin adducts exposed benzidine dihydrochloride and benzidine based dye were high level but wasn't statistically significant and those were not detected in control group.

• 한국식품영양학회지
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• 제13권3호
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• pp.242-248
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• 2000

수산물 가공시 흘러나오는 폐수 중에 함유되어 있는 수용성 단백질을 chitosan에 흡착시키기 위하여 albumin과 hemoglobin, albumin-myoglobin 혼합단백질을 이용하여 chitosan과의 흡착 및 chitosan 제조조건에 따른 흡착효과와 chitosan의 수용성 단백질 흡착에 미치는 인자를 살펴본 결과는 다음과 같다. Chitosan위 탈아세틸화 조건을 60, 70, 80%로 달리하여, albumin, hemoglobin, albumin-myoglobin 혼합용액에 적용했을때 chitosan의 탈아세틸화도가 높을수록 chitosan과 단백질 사이의 흡착률은 높게 나타났다. 초음파 처리에 의하여 chitosan의 분자량이 작을수록 chitosan과 단백질 사이의 흡착률은 높게 나타났다. pH변화에 따른 chitosan과 수용성 단백질의 흡착률은 albumin 및 albumin-myoglobin 혼합용액에서는 pH 4.0에서, hemoglobin용액에서는 pH 7.0에서 흡착률이 높게 나타났다 chitosan과 수용성단백질과의 흡착에서 반응시간은 albumin및 albumin-myoglobin 혼합용액에서는 4시간, hemoglobin용액에서는 3시간까지 흡착률이 증가하였고, 그 이후의 시간이 경화하여도 흡착률의 증가는 거의 보이지 않았다. 수용성 단백질 용액에 NaCl 농도를 0.1M에서 1.0M로 증가시켜 첨가했을때 염의 농도가 높을수록 chitosan과 단백질 사이의 흡착이 잘 일어나지 않았다.

• 한국수산과학회지
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• 제5권4호
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• pp.105-107
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• 1972

붕어(Carassius carassius), 가물치(Ophicephalus argus) 및 미꾸리(Misgurnus anguillicaudatus)의 혈색소상에 미치는 동과 염의 영향을 전분전기영동법으로 연구하였다. 1. 정상 붕어의 혈색소 band는 양극에 1개 있고, band의 수나 이동도가 동이나 염에 의하여 영향을 받지 않았다. 2. 정상 가물치의 혈색소 band는 양극 2개 있고, 이동도는 붕어와 미꾸리의 것보다 빨랐으며 동이나 염의 영향을 받지 않았다. 3 정상 미꾸리의 혈색소 band는 2개로서 양극과 음극에 1개씩 있었고, 기준선으로부터의 상대이동도는 서로 비슷하였다 미꾸리가 동에 처리된 경우 양극에 있는 band의 이동도는 대조군과 염처리군의 이동도보다 상당히 빨랐고, 한편 음극에 있는 혈색소 band는 동과 염의 영향을 받지 않았다. 이 연구를 지도하여 주신 숙명여자대학교 약학대학의 노일협박사님께 깊은 감사를 드린다.

• 동의생리병리학회지
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• 제25권4호
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• pp.697-701
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• 2011

The purpose of this study was to fine proteins, which have significantly different level in plasma between Qi-deficiency and Fire-heat group of Korean Oriental Stroke pattern identification (PI) among Korean stroke patients. Eighteen stroke patients with Qi-deficiency and forty nine patients with Fire-heat, which had critical syndrome of each PI, were participated in this study. Plasma protein pattern were analyzed by SELDI-TOF MS using Q10 strong anion exchange chip and Mass spectral data (m/z) statistically determined. The expression level of proteins, which were different between Qi-deficiency and Fire-heat in the results by SELDI-TOF MS, were confirmed by western blot. As a result of analyzing plasma protein by SELDI-TOF MS, six protein peaks were significantly higher in Fire-heat group than Qi-deficiency group. Two peaks among of them, M15003 and M15745, were respectively identified as hemoglobin alpha and beta in previous study. Expression level of plasma free hemoglobin of Fire-heat group was also confirmed higher in Fire-heat group than in Qi-deficiency group. These findings suggest that plasma free hemoglobin is a candidate for discriminating Qi-deficiency and Fire-heat group according to pattern identification (PI) of stroke.