共查询到20条相似文献,搜索用时 734 毫秒
1.
Srinivasulu S Acharya AS Prabhakaran M Fabry ME Alami R Fiering SN Bouhasirra EE Nagel RL 《The protein journal》2007,26(8):523-532
Recombinant α-Savaria globin (αS49R) was assembled with βS chains by the alloplex intermediate pathway to generate tetrameric rHbS-Sarvaria (α2S49Rβ2E6V) that exhibited normal O2 affinity and co-operatively at pH 7.4. Allosteric effectors, 2,3-DPG, L35, and NaCl increased O2 affinity by 15%. Bohr effects were similar for rHbS-Savaria and HbS (0.38 ± 0.025 vs. 0.46 ± 0.03, respectively). The CSAT of HbS increased from 16.7 ± 0.8 to 27.0 ± 1.0 g/dL. Co-polymerization demonstrated inhibition predominantly by the Cis-dimer.
Molecular modeling indicated that the positive charge at α-49 generated a strong anion-binding site and reduced flexibility
of the CD-region by restricting movement in the E and F helices. The molecular distance between Arg-49 and Asn-78 in the neighboring
double strand decreased, and electrostatic repulsion between the inter-double strands increased, resulting in inhibition of
polymerization. The Savaria mutation may be useful for the design of super-inhibitory α-chains and gene therapy of sickle
cell anemia. 相似文献
2.
Wytze T. Stam Jaap J. Beintema Rossana D’Avino Maurizio Tamburrini Guido di Prisco 《Journal of molecular evolution》1997,45(4):437-445
Amino acid sequences of α- and β-chains of human hemoglobin and of hemoglobins of coelacanth and 24 teleost fish species,
including 11 antarctic and two temperate Notothenioidei, were analyzed using maximum parsimony. Trees were derived for the
α- and β-chains separately and for tandemly arranged sequences, using the human and coelacanth sequences as outgroups in all
analyses. The topologies of the trees of the α-and β-chains are highly congruent and indicate a specific pattern of gene duplications
and gene expression of teleost hemoglobins which has not yet been investigated into more detail. The Notothenioid fish generally
contain a single major hemoglobin and often a second minor component. The α- and β-chains of the major components form a monophyletic
group in all investigated trees, with the nonantarctic Pseudaphritis as their sister taxon. The minor chains also are a monophyletic group and form an unresolved cluster with the major chains
and the hemoglobins of tuna and red gurnard. The Notothenioid families Nototheniidae and Bathydraconidae appear to be paraphyletic.
Received: 26 March 1997 / Accepted: 7 May 1997 相似文献
3.
Ola F Wetten Alexander J Nederbragt Robert C Wilson Kjetill S Jakobsen Rolf B Edvardsen Øivind Andersen 《BMC evolutionary biology》2010,10(1):315
Background
The vertebrate globin genes encoding the α- and β-subunits of the tetrameric hemoglobins are clustered at two unlinked loci. The highly conserved linear order of the genes flanking the hemoglobins provides a strong anchor for inferring common ancestry of the globin clusters. In fish, the number of α-β-linked globin genes varies considerably between different sublineages and seems to be related to prevailing physico-chemical conditions. Draft sequences of the Atlantic cod genome enabled us to determine the genomic organization of the globin repertoire in this marine species that copes with fluctuating environments of the temperate and Arctic regions. 相似文献4.
Osamu Takenaka Mika Hotta Akiko Takenaka Yoshi Kawamoto Bambang Suryobroto Edy Brotoisworo 《Primates; journal of primatology》1987,28(1):87-98
The monkeys on the island of Sulawesi (Celebes), Indonesia, comprise seven species ofMacaca, that isM. maura, M. tonkeana, M. hecki, M. nigrescens, M. nigra, M. ochreata, andM. brunnescens. Hemoglobins from 248 individuals of these seven species were analyzed by isoelectric focusing electrophoresis (IEFE) and
by starch gel electrophoresis in the presence of urea (USGE). Eighteen phenotypes consisting of eight molecular types were
identified by IEFE analysis. The speciestonkeana inhabiting the central part of the island revealed 11 phenotypes, while peripheral species such asnigrescens andbrunnescens carried only 3 and 2 phenotypes, respectively.
On USGE, three α chains and three β chains were identified and named α1, α2, and α6, and β1, β3, and β5, respectively. The
α1 chain has the same mobility as the α chains of other macaques, while the α2 chain is less positively charged than α1, and
α6 is the least positive among these α chains. The α2 chain is widely distributed in the Sulawesi macaques as the major component.
Four species,ochreata, tonkeana, maura, andnigrescens, carried the α1 and α6 chains as minor components. The electrophoretic mobility of β1 was the same as that of other macaques,
while β3 and β5 were more positively charged and less positively charged than β1, respectively. All of the Sulawesi species
had β3 in high or low gene frequencies and inmaura, tonkeana, andbrunnescens, this type was most abundant. β5 chain existed in the species of the northern peninsula, as the major type. The subordinate
type was β3 innigra andnigrescens and β1 inhecki. On the other hand, β1 was most frequently observed inochreata. 相似文献
5.
Three highly heterogeneous haemoglobin phenotypes, each composed of 22 different haemoglobin components, were identified among 17 West African populations of Sarotherodon melanotheron . Natural populations from (1) Senegal, (2) Ivory Coast/Ghana/Togo/Benin, and (3) Congo were distinguished. The heterogeneity and specificity of these respiratory pigments was based on genetic variations at the globin chain coding loci. In total, five different α-chains and four different β-chains were detected by acidic urea polyacrylamide gel electrophoresis (PAGE). Combinations of α-chains were characteristic for populations in (1) Senegal, (2) Ivory Coast, (3) Ghana/Togo/Benin, and (4) Congo. Pronounced variations at the β-globin chain cluster were found by acidic urea triton PAGE. Cladistic analyses of the globin chain characteristics confirmed the validity of the following taxonomic units previously ranked as sub-species: (1) populations from Ivory Coast, Ghana, Togo and Benin belong to the sub-species S. m. melanotheron ; (2) populations from Senegal form genetically a separate cluster representing the sub-species S. m. heudelotii ; (3) the Congo population, morphologically considered to represent the sub-species S. m. nigripinnis , forms another distinct unit; but there was no evidence of S. m. paludinosus within the samples from Senegal. 相似文献
6.
Barbara Manconi Irene Messana Federica Maggiani Alessandra Olianas Mariagiuseppina Pellegrini Roberto Crnjar Massimo Castagnola Bruno Giardina Maria Teresa Sanna 《Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology》2009,179(8):971-983
Structural analysis of the hemoglobin (Hb) system of Delphinus delphis revealed a high globin multiplicity: HPLC–electrospray ionization-mass spectrometry (ESI-MS) analysis evidenced three major
β (β1 16,022 Da, β2 16,036 Da, β3 16,036 Da, labeled according to their progressive elution times) and two major α globins
(α1 15,345 Da, α2 15,329 Da). ESI-tandem mass and nucleotide sequence analyses showed that β2 globin differs from β1 for the
substitution Val126 → Leu, while β3 globin differs from β2 for the isobaric substitution Lys65 → Gln. The α2 globin differs
from the α1 for the substitution Ser15 → Ala. Anion-exchange chromatography allowed the separation of two Hb fractions and
HPLC–ESI-MS analysis revealed that the fraction with higher pI (HbI) contained β1, β2 and both the α globins, and the fraction with lower pI (HbII) contained β3 and both the α globins. Both D. delphis Hb fractions displayed a lower intrinsic oxygen affinity, a decreased effect of 2,3-BPG and a reduced cooperativity with
respect to human HbA0, with HbII showing the more pronounced differences. With respect to HbA0, either the substitution Proβ5 → Gly or the Proβ5 → Ala is present in all the cetacean β globins sequenced so far, and it
has been hypothesized that position 5 of β globins may have a role in the interaction with 2,3-BPG. Regarding the particularly
lowered cooperativity of HbII, it is interesting to observe that the variant human HbA, characterized by the substitution
Lysβ65 → Gln (HbJ-Cairo) has a decreased cooperativity with respect to HbA0. 相似文献
7.
Gurusamy Balakrishnan Mohammed Ibrahim Piotr J. Mak Jessica Hata James R. Kincaid Thomas G. Spiro 《Journal of biological inorganic chemistry》2009,14(5):741-750
Time-resolved resonance Raman (RR) spectra are reported for hemoglobin (Hb) tetramers, in which the α and β chains are selectively
substituted with mesoheme. The Soret absorption band shift in mesoheme relative to protoheme permits chain-selective recording
of heme RR spectra. The evolution of these spectra following HbCO photolysis shows that the geminate recombination rates and
the yields are the same for the two chains, consistent with recent results on 15N-heme isotopomer hybrids. The spectra also reveal systematic shifts in the deoxyheme ν
4 and ν
Fe–His RR bands, which are anticorrelated. These shifts are resolved for the successive intermediates in the protein structure,
which have previously been determined from time-resolved UV RR spectra. Both chains show Fe–His bond compression in the immediate
photoproduct, which relaxes during the formation of the first intermediate, Rdeoxy (0.07 μs), in which the proximal F-helix is proposed to move away from the heme. Subsequently, the Fe–His bond weakens, more
so for the α chains than for the β chains. The weakening is gradual for the β chains, but is abrupt for the α chains, coinciding
with completion of the R–T quaternary transition, at 20 μs. Since the transition from fast- to slow-rebinding Hb also occurs
at 20 μs, the drop in the α chain ν
Fe–His supports the localization of ligation restraint to tension in the Fe–His bond, at least in the α chains. The mechanism is
more complex in the β chains. 相似文献
8.
Mycorrhizal and nonmycorrhizal roots of Allium schoenoprasum were tested for activities of α-mannosidase, β-glucosidase and arabinosidase. Mannosidase activity was higher by a factor
of two in mycorrhizal than in nonmycorrhizal root extracts. The apparent molecular weight of the enzyme was 152 kDa and its
KM was 1.25 mM in colonized roots and 1.85 mM in uncolonized roots. α-Mannosidase activity was further characterized by an acid
pH optimum and Zn2+ dependency. No significant differences could be found between mycorrhizal and nonmycorrhizal roots for β-glucosidase and
arabinosidase activities.
Accepted: 28 August 1995 相似文献
9.
Daniela Giordano Luigi Grassi Elio Parisi Luca Bargelloni Guido di Prisco Cinzia Verde 《Polar Biology》2006,30(1):75-82
Haemoglobins are sensitive to temperature and their properties mirror the thermal conditions encountered by species during their evolutionary histories. This paper provides data on molecular phylogeny of the haemoglobin chains of Cottoperca gobio, a notothenioid fish of sub-Antarctic latitudes, belonging to the basal family Bovichtidae. Unlike most Antarctic notothenioids, C. gobio has two major haemoglobins sharing the β chain. In the molecular phylogenetic analysis, the β chain is included in the clade of the “embryonic” or minor Antarctic globins. Although, in the majority of notothenioids, “embryonic” (minor) α and β globins are expressed in traces or small amounts in the adult stage, in C. gobio the present analysis supports the occurrence of a complete “switch” to exclusive expression of the embryonic β-globin gene in adult fish. The α and β chains sequences have been used to expand our knowledge of the evolution of notothenioid haemoglobins.The protein sequence data reported in this paper will appear in the UniProt Knowledge base under the accession number: P84652 (β chain), P84653 (α
1
chain). 相似文献
10.
E. Sandmeier D. Gygi T. Wyler U. Nyffenegger R. Weber 《Development genes and evolution》1988,197(7):406-412
Summary High-resolution electrophoresis of larval and adult hemoglobins of Xenopus laevis reveals stage-specific differences in the number and mobility of the globin chains. To establish the relationship between the globin chains and the previously described globin genes, the corresponding mRNAs were hybrid-selected from total erythroblast RNA by representative cDNA clones, and translated in vitro. Electrophoretic separation of the translation products allowed identification of a major and a minor -globin chain in the larval and adult stages. This also holds for the adult -chains, however in the larval stage a difference in abundance is only detectable in the -mRNAs, but not in the translation products, because they comigrate. The fact that major and minor globin chains can be assigned to genes, which are located in two clusters, suggests that the related genes are expressed coordinately, but at different levels. Analysis of the globin patterns during development reveals that transition from the larval to the adult globin chains coincides with metamorphosis. Moreover, there is evidence of two globin chains that are only expressed in early larval stages and hence might be related to additional larval -globin genes of as yet unknown genomic location. 相似文献
11.
Stefanie Henning Michael Mormann Jasna Peter-Katalinić Gottfried Pohlentz 《Amino acids》2011,41(2):343-350
α- and β-chains of hemoglobins derived from several species were analyzed directly from diluted blood samples by simultaneous
in-capillary proteolytic digestion and nanoESI MS and MS/MS analysis. Starting from fresh or frozen and thawed blood samples,
sequence coverages of >80% were usually obtained. Only 2 h after resuspension of a dried blood spot, human origin could be
demonstrated from data obtained by in-capillary tryptic digestion, nanoESI mass spectrometric analysis, and data base search.
A fast and facile differentiation of closely related species by hemoglobin-derived proteolytic “marker peptides” was demonstrated
for Asian (Elephas maximus) and African elephants (Loxodonta africana). Finally, amino acid sequences deduced from collision-induced dissociation experiments during in-capillary proteolytic digestion
of the corresponding blood samples allowed de novo sequencing of previously unknown sequences of hemoglobin chains of the
Patagonian cavy (Dolichotum patagona) and the Persian gazelle (Gazella subgutturosa subgutturosa). 100% of the α-chain sequences and more than 85% of the β-chain sequences were covered for both the species. Additionally,
sequence data derived from tandem MS experiments obtained with the Q-Tof analyzer were confirmed by high resolution Fourier-transform
ion cyclotron resonance mass spectrometric experiments. Accurate protein mass determination of the intact hemoglobin chains
directly from the corresponding blood samples by use of a Fourier-transform ion cyclotron resonance mass spectrometer corroborated
the deduced sequences of the respective α-chains. The present study demonstrates that in-capillary digestion allows fast characterization
and/or sequencing of hemoglobin chains directly from blood samples. 相似文献
12.
The evolutionary origin of murine line based on a phylogenetic tree made on sequence data of ∞-and β-hemoglobin chains, followed
by the diversity spectrum of hemoglobin genes in two wild species of murine rodents:Rattus rattus rufescens (house rat) andBandicota indica (bandicoot rat) has been reported. Each house rat contains six hemoglobin types involving two ∞-and three β-chains, which
suggests a probable gene duplication at the oc chain locus and a gene triplication at the β-chain locus. Each bandicoot rat
contains one ∞-and two β-chains suggesting a probable gene duplication at the β-chain locus. Peptide pattern analysis of the
polypeptide chains of these murine hemoglobins further indicates that intraspecies differences among duplicated chains of
the same kind are less than interspecies differences among corresponding ∞-and β-chains. 相似文献
13.
Kubiński K Domańska K Sajnaga E Mazur E Zieliński R Szyszka R 《Molecular and cellular biochemistry》2007,295(1-2):229-236
Protein kinase CK2 is a highly conserved Ser/Thr protein kinase that is ubiquitous among eucaryotic organisms and appears
to play an important role in many cellular functions. This enzyme in yeast has a tetrameric structure composed of two catalytic
(α and/or α′) subunits and two regulatory β and β′ subunits. Previously, we have reported isolation from yeast cells four
active forms of CK2, composed of αα′ββ′, α2ββ′, α′2ββ′ and a free α′-catalytic subunit. Now, we report that in Saccharomyces cerevisiae CK2 holoenzyme regulatory β subunit cannot substitute other β′ subunit and only both of them can form fully active enzymatic
unit. We have examined the subunit composition of tetrameric complexes of yeast CK2 by transformation of yeast strains containing
single deletion of the β or β′ regulatory subunits with vectors carrying lacking CKB1 or CKB2 genes. CK2 holoenzyme activity was restored only in cases when both of them were present in the cell. Additional, co-immunoprecypitation
experiments show that polyadenylation factor Fip1 interacts with catalytic α subunits of CK2 and interaction with beta subunits
in the holoenzyme decreases CK2 activity towards this protein substrate. These data may help to elucidate the role of yeast
protein kinase CK2β/β′ subunits in the regulation of holoenzyme assembly and phosphotransferase activity. 相似文献
14.
J. Q. Liu S. Ito T. Dairi N. Itoh S. Shimizu H. Yamada 《Applied microbiology and biotechnology》1998,49(6):702-708
Low-specificity l-threonine aldolase, catalyzing the reversible cleavage/condensation reaction between l-threonine/l-allo-threonine and glycine plus acetaldehyde, was purified to homogeneity from Pseudomonas sp. NCIMB 10558. The enzyme has an apparent molecular mass of approximately 145 kDa and consists of four identical subunits
with a molecular mass of 38 kDa. The enzyme, requiring pyridoxal- 5′-phosphate as a coenzyme, is strictly l-specific at the α position, whereas it can not distinguish between threo and erythro forms at the β position. Besides the reversible cleavage/condensation of threonine, the enzyme also catalyzes the reversible
interconversion between glycine plus various aldehydes and l-β-hydroxy-α-amino acids, including l-β-(3,4-dihydroxyphenyl)serine, l-β-(3,4-met‐hylenedioxyphenyl)serine and l-β-phenylserine, providing a new route for the industrial production of these important amino acids.
Received: 10 November 1997 / Received revision: 7 January 1998 / Accepted 30 January 1998 相似文献
15.
Presence and stability of an unusual phycoerythrin (PE) characteristically similar to R-PE are described in a terrestrial,
desiccation-tolerant cyanobacterium, Lyngbya arboricola. Extraction and purification of the PE by using acetone precipitation, gel filtration and ion-exchange chromatography resulted
in achieving a purity index (A560/A280) of up to 5.2. SDS-PAGE of the PE showed presence of 18 kDa, 20 kDa and 32 kDa bands corresponding to α, β and γ subunits
of R-PE without any other contaminating phycobiliproteins (PBPs). The absorption spectrum of the PE was distinguished by two
major peaks at 499 and 559 nm. The maximum fluorescence emission at room temperature was 578 nm. Spectroscopic and electrophoresis
characteristics of PE in the dry mats on storage at 25 ± 1°C over silica gel for 2 years remained almost unaffected. Quantitatively,
storage stability of the PE was in the order of dry mats > lyophilized > liquid state and the impact of temperature on loss
of PE was in the order of 25°C > −20°C > 4°C. The relevance of L. arboricola for production of stable unusual PE is discussed. 相似文献
16.
Solute mobilities in cuticular membranes of six species (Hedera helix, Malus domestica, Populus alba, Pyrus communis, Stephanotis floribunda, Strophantus gratus) were measured using plant hormones, growth regulators and other organic model compounds varying in molar volumes from 99
to 349 mL · mol−1 The dependence of mobilities (k*) on molar volume (V
x
) was exponential and could be described with equations of the type log
k*=log
k*0−′
V
x
. The y-intercepts (log
k*0) represent mobilities of a hypothetical solute of zero molar volume. The parameter β′ is a measure of size selectivity of
cuticular membranes and no differences among the six species were observed. At 25 °C the average β′ was 0.0095 mol · mL−1. Solute mobility decreased by about a factor of 8.9 when molar volume increased by 100 mL · mol−1 and the mobility of a compound with V
x
= 100 mL · mol−1 was about 700-fold higher than the mobility of a compound with V
x
= 400 mL · mol−1. Size selectivity decreased with increasing temperatures and for Strophantusβ′-values of 1.6 × 10−2 to 8.0 × 10-4 mol · mL−1 were obtained for 10 and 30 °C, respectively. The-intercepts (log k*0) differed among plant species by 3 orders of magnitude and since size selectivity was the same for all species, solute mobilities
for solutes having zero molar volumes were the sole cause for differences among species in solute mobilities and permeabilities.
We argue that these differences in k*0 are related to tortuosity of the diffusion path. These results were used to derive an equation which predicts rates of cuticular
penetration on the basis of k*0, the average size selectivity of 9.5 × 10−3 mol · mL−1 and the driving forces of penetration.
Received: 25 November 1997 / Accepted: 9 March 1998 相似文献
17.
Light-regulated localization of the beta-subunit of Gq-type G-protein in the crayfish photoreceptors 总被引:3,自引:0,他引:3
A. Terakita H. Takahama T. Hariyama T. Suzuki Y. Tsukahara 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1998,183(4):411-417
In crayfish photoreceptor cells, Gq-type G-protein plays a central role in the phototransduction pathway, and the translocation
of Gqα has been proposed as one of the molecular mechanisms to control photoreceptor sensitivity. We here investigated β subunit
of Gq and its localization profiles under various light conditions in the crayfish photoreceptor cells to understand the functional
characteristic of visual Gq in the phototransduction pathway. An immunoprecipitation experiment was performed using an anti-Gqα
antibody and a thiol-cleavable crosslinker. A 39 kDa protein was co-immunoprecipitated with Gqα, but not by irradiation, in
the presence of GTPγS. The partial amino acid sequence of the 39 kDa protein was similar to Gβe in Drosophila photoreceptors, indicating that the crayfish Gβ which combines with Gqα is a Gβe homologue. Immunohistochemical and immunoblot
analyses revealed that the amount of the Gβ decreased in the rhabdomeric membranes and increased in the cytoplasm in the light,
compared with that in the dark. The profile of the translocation was similar to that reported for Gqα. Since both α and βγ
subunits are necessary for G-proteins to be activated by rhodopsin in the rhabdom, the light-modulated translocation of a
Gβe homologue possibly controls the amount of Gq which can be activated by light-stimulated rhodopsin.
Accepted: 27 June 1998 相似文献
18.
M. J. Artolozaga E. Kubátová J. Volc H. M. Kalisz 《Applied microbiology and biotechnology》1997,47(5):508-514
Pyranose 2-oxidase (P2O) was purified 43-fold to apparent homogeneity from the basidiomycete Phanerochaete chrysosporium using liquid chromatography on phenyl Sepharose, Mono Q (twice) and phenyl Superose. The native enzyme has a molecular mass
of about 250 kDa (based on native PAGE) and is composed of four identical subunits of 65 kDa. It contains three isoforms of
isoelectric point (pI) 5.0, 5.05 and 5.15 and does not appear to be a glycoprotein. P2O is optimally stable at pH 8.0 and
up to 60 °C. It is active over a broad pH range (5.0–9.0) with maximum activity at pH 8.0–8.5 and at 55 °C, and a broad substrate
specificity. d-Glucose is the preferred substrate, but 1-β-aurothioglucose, 6-deoxy-d-glucose, l-sorbose, d-xylose, 5-thioglucose, d-glucono-1,5-lactone, maltose and 2-deoxy-d-glucose are also oxidised at relatively high rates. A Ping Pong Bi Bi mechanism was demonstrated for the P2O reaction at
pH 8.0, with a catalytic constant (k
cat) of 111.0 s−1 and an affinity constant (K
m) of 1.43 mM for d-glucose and 83.2 μM for oxygen. Whereas the steady-state kinetics for glucose oxidation were unaffected by the medium at
pH ≥ 7.0, at low pH both pH and buffer composition affected the P2O kinetics with the k
cat/K
m value decreasing with decreasing pH. The greatest effect was observed in acetate buffer (0.1 M, pH 4.5), where the k
cat decreased to 60.9 s−1 and the K
m increased to 240 mM. The activity of P2O was completely inhibited by 10 mM HgCl2, AgNO3 and ZnCl2, and 50% by lead acetate, CuCl2 and MnCl2.
Received: 28 August 1996 / Received revision: 25 November 1996 / Accepted: 29 November 1996 相似文献
19.
Srinivasulu S Perumalsamy K Upadhya R Manjula BN Feiring S Alami R Bouhassira E Fabry ME Nagel RL Acharya AS 《The protein journal》2006,25(7-8):503-516
The linkage of pair-wise interactions of contact site mutations of HbS has been studied using Le Lamentin [His-20 (α)→Gln], Hoshida [Glu-43 (β)→Gln] and α2β2T87Q mutations as the prototype of three distinct classes of contact sites of deoxy HbS fiber. Binary mixture experiments established that βA-chain with the Thr-87 (β)→Gln mutation is as potent as the γ-chain of HbF (α2γ2) in inhibiting polymerization. On combining the influence of Le Lamentin mutation with that of β2T87Q mutations; the net influence is only partial additivity. On the other hand, in binary mixture studies, combined influence of Hoshida mutation with that of β2T87Q mutations is synergistic. Besides, a significant level of synergistic complementation is also seen when the Le Lamentin and Hoshida mutations are combined in HbS (symmetrical tetramers). Le Lamentin and Hoshida mutation introduced into the cis-dimer of the asymmetric hybrid tetramer completely neutralizes the Val-6 (β) dependent polymerization. Accordingly, we propose that combining the perturbation of intra-double strand contact site with that of an inter-double strand contact site exhibit synergy when they are present in two different chains of the αβ dimer. A comparison of the present results with that of the earlier studies suggest that when the two contact site perturbations are from the same sub-unit of the αβ dimer only partial additivity is observed. The map of interaction linkage of the contact site mutations exposes new strategies in the design of novel anti-sickling Hbs for the gene therapy of sickle cell disease. 相似文献
20.
The complete primary structure of the hemoglobin from the adult coati (Nasua nasua rufa) is presented. The erythrocytes contain one hemoglobin component and two globin chains. The isolation of globin chains was achieved by reversed-phase HPLC on a column of Nucleosil-C4. The primary structure of globin chains and tryptic peptides was determined in liquid- and gas-phase sequenators. The sequence of the and -chains of coati compared with those of other Carnivora species. Results are discussed with respect to structural variations and the phylogenetic relationship.Deceased on May 27, 1989. 相似文献