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PubMed1975

Carrier-mediated transfer of D-glucose in brush border vesicles derived from rabbit renal tubules. Na+-dependent versus Na+-independent transfer.

A brush border preparation from rabbit renal tubules containing a high yield of vesicles has been used to study the transfer of D-glucose through the brush border membrane. In the presence of an Na+ gradient across the vesicular membrane, the vesicles could concentrate D-glucose to a factor of 1.5, whereas in the absence of an Na+ gradient, only equilibrium with the medium was achieved. Two types of transfer could be distinguished by their requirement of Na+, their sensitivity to phlorizin and their pH optimum. The Na+-independent transfer was about 100 times less sensitive to phlorizin than the Na+-dependent path and exhibited a pH optimum between 7 and 8, whereas the Na+-dependent transfer was highest at a pH between 8 and 9. The brush border preparation could be freed of most of the contaminating material derived from the basal and lateral tubular cell membrane by a discontinuous density gradient centrifugation. It still showed both forms of transfer to a similar extent, indicating that both are located in the brush border membrane. A study of the sensitivity of D-glucose transfer to phlorizin, in the presence and absence of Na+ at different temperature, suggests a single carrier species functioning in two interchangeable conformational states with different affinities for phlorizin rather than two transfer systems working independently.

Adenosine Triphosphatases↗

PubMed2004

Theory and simulation of proton-coupled electron transfer, hydrogen-atom transfer, and proton translocation in proteins.

A theory of proton coupled electron transfer (PCET) is reviewed with application to charge transfer steps in the photosystem II oxygen-evolving complex (PSII/OEC). The relation between PCET when it is a concerted electron proton transfer (ETPT) process and hydrogen-atom transfer (HAT) reactions is discussed. Signatures expected for HAT reactions in terms of the size of the kinetic isotope effect and overall magnitude of the rate constant are discussed in the context of PSII/OEC. The formal similarity of ETPT to proton transfer and translocation is used to introduce a combined quantum mechanical (for the transferring protons) and molecular dynamics for the heavy-atom degrees of freedom approach. The method is used to examine double proton transfer in cytochrome c oxidase where two waters and a glutamate (Glu286) that is implicated in the proton translocation mechanism form a cyclic hydrogen bonded structure. Protonation of the glutamate is found to occur in agreement with experimental results.

Electron Transport↗

PubMed2004

Proton transfer to nickel-thiolate complexes. 2. Rate-limiting intramolecular proton transfer in the reactions of [Ni(SC(6)H(4)R-4)(PhP[CH(2)CH(2)PPh(2)](2))](+) (R = NO(2), Cl, H, Me, or MeO).

The protonation of [Ni(SC(6)H(4)R-4)(triphos)](+) (triphos = PhP[CH(2)CH(2)PPh(2)](2); R = NO(2), Cl, H, Me, or MeO) by [lutH](+) (lut = 2,6-dimethylpyridine) to form [Ni(S(H)C(6)H(4)R-4)(triphos)](2+) is an equilibrium reaction in MeCN. Kinetic studies, using stopped-flow spectrophotometry, reveal that the reactions occur by a two-step mechanism. Initially, [lutH](+) rapidly binds to the complex (K(2)(R)) in an interaction which probably involves hydrogen-bonding of the acid to the sulfur. Subsequent intramolecular proton transfer from [lutH](+) to sulfur (k(3)(R)) is slow because of both electronic and steric factors. The X-ray crystal structures of [Ni(SC(6)H(4)R-4)(triphos)](+) (R = NO(2), H, Me, or MeO) show that all are best described as square-planar complexes, with the phenyl substituents of the triphos ligand presenting an appreciable barrier to the approach of the sterically demanding [lutH](+) to the sulfur. The kinetic characteristics of the intramolecular proton transfer from [lutH](+) to sulfur have been investigated. The rate of intramolecular proton transfer exhibits a nonlinear dependence on Hammett sigma(+), with both electron-releasing and electron-withdrawing 4-R-substituents on the coordinated thiolate facilitating the rate of proton transfer (NO(2) > Cl > H > Me < MeO). The rate constants for intramolecular proton transfer correlate well with the calculated electron density of the sulfur. The temperature dependence of the rate of the intramolecular proton transfer reactions shows that deltaH() is small but increases as the 4-R-substituent becomes more electron-withdrawing [deltaH = 4.1 (MeO), 6.9 (Me), 11.4 kcal mol(-)(1) (NO(2))], while DeltaS() becomes progressively less negative [deltaS = -50.1 (MeO), -41.2 (Me), -16.4 (NO(2)) cal K(-)(1) mol(-)(1)]. Studies with [lutD](+) show that the rate of intramolecular proton transfer varies with the 4-R-substituent [(k(3)(NO)2)(H)/(k(3)(NO)2)(D) = 0.39; (k(3)(Cl))(H)/(k(3)(Cl))(D) = 0.88; (k(3)(Me))(H)/(k(3)(Me))(D) = 1.3; (k(3)(MeO))(H)/(k(3)(MeO))(D) = 1.2].

Journal Article↗

PubMed2005

Oxidations of NADH analogues by cis-[RuIV(bpy)2(py)(O)]2+ occur by hydrogen-atom transfer rather than by hydride transfer.

Oxidations of the NADH analogues 10-methyl-9,10-dihydroacridine (AcrH2) and N-benzyl 1,4-dihydronicotinamide (BNAH) by cis-[RuIV(bpy)2(py)(O)]2+ (RuIVO2+) have been studied to probe the preferences for hydrogen-atom transfer vs hydride transfer mechanisms for the C-H bond oxidation. 1H NMR spectra of completed reactions of AcrH2 and RuIVO2+, after more than approximately 20 min, reveal the predominant products to be 10-methylacridone (AcrO) and cis-[RuII(bpy)2(py)(MeCN)]2+. Over the first few seconds of the reaction, however, as monitored by stopped-flow optical spectroscopy, the 10-methylacridinium cation (AcrH+) is observed. AcrH+ is the product of net hydride removal from AcrH2, but hydride transfer cannot be the dominant pathway because AcrH+ is formed in only 40-50% yield and its subsequent oxidation to AcrO is relatively slow. Kinetic studies show that the reaction is first order in both RuIVO2+ and AcrH2, with k = (5.7 +/- 0.3) x 10(3) M(-1) s(-1) at 25 degrees C, DeltaH(double dagger) = 5.3 +/- 0.3 kcal mol(-1) and DeltaS(double dagger) = -23 +/- 1 cal mol(-1) K(-1). A large kinetic isotope effect is observed, kAcrH2/kAcrD2 = 12 +/- 1. The kinetics of this reaction are significantly affected by O2. The rate constants for the oxidations of AcrH2 and BNAH correlate well with those for a series of hydrocarbon C-H bond oxidations by RuIVO2+. The data indicate a mechanism of initial hydrogen-atom abstraction. The acridinyl radical, AcrH*, then rapidly reacts by electron transfer (to give AcrH+) or by C-O bond formation (leading to AcrO). Thermochemical analyses show that H* and H- transfer from AcrH2 to RuIVO2+ are comparably exoergic: DeltaG degrees = -10 +/- 2 kcal mol(-1) (H*) and -6 +/- 5 kcal mol(-1) (H-). That a hydrogen-atom transfer is preferred kinetically suggests that this mechanism has an equal or lower intrinsic barrier than a hydride transfer pathway.

Acridines↗

PubMed2004

Evidence for through-space electron transfer in the distance dependence of normal and inverted electron transfer in oligoproline arrays.

Four new helical oligoproline assemblies containing 16, 17, 18, and 19 proline residues and ordered arrays of a Ru(II)-bipyridyl chromophore and a phenothiazine electron-transfer donor have been synthesized in a modular fashion by solid-phase peptide synthesis. These arrays are illustrated and abbreviated as CH(3)CO-Pro(6)-Pra(PTZ)-Pro(n)()-Pra(Ru(II)b(2)m)(2+)-Pro(6)-NH(2), where PTZ is 3-(10H-phenothiazine-10)propanoyl and (Ru(II)b'(2)m)(2+) is bis(4,4'-diethylamide-2,2'-bipyridine)(4-methyl,4'-carboxylate,2,2'-bipyridine)ruthenium(II) dication with n = 2 (2), 3 (3), 4 (4), and 5 (5). They contain PTZ as an electron-transfer donor and (Ru(II)b'(2)m)(2+) as a metal-to-ligand charge transfer (MLCT) light absorber and are separated by proline-to-proline through-space distances ranging from 0 (n = 2) to 12.9 A (n = 5) relative to the n = 2 case. They exist in the proline-II helix form in water, as shown by circular dichroism measurements. Following laser flash Ru(II) --> b'(2)m MLCT excitation at 460 nm in water, excited-state PTZ --> Ru(2+) quenching (k(2)) occurs by reductive electron transfer, followed by Ru(+) --> PTZ(+) back electron transfer (k(3)), as shown by transient absorption and emission measurements in water at 25 degrees C. Quenching with DeltaG degrees = -0.1 eV is an activated process, while back electron transfer occurs in the inverted region, DeltaG degrees = -1.8 eV, and is activationless, as shown by temperature dependence measurements. Coincidentally, both reactions have comparable distance dependences, with k(2)( )()varying from = 1.9 x 10(9) (n = 2) to 2.2 x 10(6) s(-)(1) (n = 4) and k(3) from approximately 2.0 x 10(9) (n = 2) to 2.2 x 10(6) s(-)(1) (n = 4). For both series there is a rate constant enhancement of approximately 10 for n = 5 compared to n = 4 and a linear decrease in ln k with the through-space separation distance, pointing to a significant and probably dominant through-space component to intrahelical electron transfer.

Electrons↗

PubMed2005

Transfer of photoenergy in pi-conjugated polymers. Two types of photoluminescence that involve energy transfer along a polymer chain.

Two types of energy transfer in pi-conjugated polymers have been investigated using time-resolved photoluminescence (PL) techniques: type i, perpendicular-type energy transfer from the 2,3-di(p-tolyl)quinoxaline unit to the pi-conjugated main chain of poly[2,3-di(p-tolyl)quinoxaline-5,8-diyl], and type ii, parallel-type energy transfer from the oligo(pyridine-2,5-diyl) (O-Py) unit to the oligo(selenophene-2,5-diyl) (O-Se) unit in a block-type copolymer of O-Py and O-Se. Both types of energy transfer were very fast with a time constant shorter than approximately 0.1 ns; in particular, the type ii energy transfer took place with a time constant of approximately 5 ps. Both pi-conjugated polymers were considered to contain segments with various effective pi-conjugation lengths, and the energy transfer to the segment with a larger effective pi-conjugation length and a smaller pi-pi* transition energy required a longer transition time. A polarizing film was obtained by utilizing the perpendicular-type energy transfer.

Journal Article↗

PubMed2006

Light-harvesting energy transfer and subsequent electron transfer of cationic porphyrin complexes on clay surfaces.

A novel energy-transfer system involving nonaggregated cationic porphyrins adsorbed on an anionic-type clay surface and the electron-transfer reaction that occurs after light harvesting are described. In the clay-porphyrin complexes, photochemical energy transfer from excited singlet zinc porphyrins to free-base porphyrins proceeds. The photochemical electron-transfer reaction from an electron donor in solution (hydroquinone) to the adsorbed porphyrin in the excited singlet state was also examined. Because the electron-transfer rate from the hydroquinone to the excited singlet free-base porphyrin is larger than that to the excited singlet zinc porphyrin, we conclude that the energy transfer accelerates the overall electron-transfer reaction.

Aluminum Silicates↗

PubMed2004

Molecular dynamics investigation of ferrous-ferric electron transfer in a hydrolyzing aqueous solution: calculation of the pH dependence of the diabatic transfer barrier and the potential of mean force.

We present a molecular model for ferrous-ferric electron transfer in an aqueous solution that accounts for electronic polarizability and exhibits spontaneous cation hydrolysis. An extended Lagrangian technique is introduced for carrying out calculations of electron-transfer barriers in polarizable systems. The model predicts that the diabatic barrier to electron transfer increases with increasing pH, due to stabilization of the Fe3+ by fluctuations in the number of hydroxide ions in its first coordination sphere, in much the same way as the barrier would increase with increasing dielectric constant in the Marcus theory. We have also calculated the effect of pH on the potential of mean force between two hydrolyzing ions in aqueous solution. As expected, increasing pH reduces the potential of mean force between the ferrous and ferric ions in the model system. The magnitudes of the predicted increase in diabatic transfer barrier and the predicted decrease in the potential of mean force nearly cancel each other at the canonical transfer distance of 0.55 nm. Even though hydrolysis is allowed in our calculations, the distribution of reorganization energies has only one maximum and is Gaussian to an excellent approximation, giving a harmonic free energy surface in the reorganization energy F(DeltaE) with a single minimum. There is thus a surprising amount of overlap in electron-transfer reorganization energies for Fe(2+)-Fe(H2O)6(3+), Fe(2+)-Fe(OH)(H2O)5(2+), and Fe(2+)-Fe(OH)2(H2O)+ couples, indicating that fluctuations in hydrolysis state can be viewed on a continuum with other solvent contributions to the reorganization energy. There appears to be little justification for thinking of the transfer rate as arising from the contributions of different hydrolysis states. Electronic structure calculations indicate that Fe(H2O)6(2+)-Fe(OH)n(H2O)(6-n)(3-n)+ complexes interacting through H3O2- bridges do not have large electronic couplings.

Journal Article↗

PubMed1985

Rate of cholesteryl ester transfer between high and low density lipoproteins in human serum and a case with decreased transfer rate in association with hyperalphalipoproteinemia.

The rate of cholesteryl ester transfer between intrinsic high and low density lipoproteins (HDL and LDL) was measured in human serum in the absence of lecithin:cholesterol acyltransferase (LCAT) and very low density lipoproteins. The rate was calculated according to the equilibrium transfer model between the two lipoprotein cholesteryl ester pools. The average rate of the transfer was 213 +/- 95 nmol/h/ml (mean +/- S.E.) for all 20 normal and 13 hyperlipoproteinemic subjects. The transfer rate in individual serum was higher by several times than the cholesterol esterification rate, showing that cholesteryl ester generated by LCAT on HDL is promptly distributed among various lipoprotein subclasses. The rate of cholesteryl ester transfer in the serum was significantly proportional to the product of intrinsic HDL and LDL concentrations, a possible indicator of the frequency of collision between these lipoproteins, for the range of physiological lipoprotein concentrations. Among the subjects analyzed was a patient with remarkable hyperalphalipoproteinemia accompanied by hypertriglyceridemia, who showed a very low rate of cholesteryl ester transfer in relation to his LDL and HDL concentrations. Compositional analysis of lipoprotein lipids of the patients also supported the possibility of impaired neutral lipids transfer activity among lipoproteins in the blood.

Adult↗

PubMed1994

Phospholipid binding and transfer by the nonspecific lipid-transfer protein (sterol carrier protein 2). A kinetic model.

The nonspecific lipid-transfer protein (nsL-TP) from bovine liver was studied by measuring the binding and transfer of the fluorescent phospholipid 1-palmitoyl-2-[6-(1-pyrenyl)-hexanoyl]-sn-glycero-3-phosphocholine (PamPryGroPCho). A kinetic model is presented involving three steps: (a) interaction of nsL-TP with a membrane surface; (b) equilibration of PamPyrGroPCho monomers between the membrane and nsL-TP; and (c) dissociation of the nsL-TP/PamPyrGroPCho complex from the membrane surface. Steady-state analysis of the model yielded theoretical equations describing both binding and transfer kinetics. Computer analysis, using these equations, showed good fits with the experimental results and several kinetic constants could be calculated. From these constants it was inferred that incorporation of acidic phospholipids into vesicles enhanced the interaction of nsL-TP with the membrane interface (step a), without affecting the equilibrium binding of phospholipid monomers to nsL-TP (step b). As a result, the rate of nsL-TP-mediated PamPyrGroPCho transfer from donor to acceptor vesicles was greatly affected. Under the conditions of incubation, incorporation of the acidic lipids in the donor membrane vesicles stimulated transfer, whereas incorporation of these lipids in the acceptor membranes could lead to a virtually complete inhibition of transfer. From the results it is concluded that the formation of a soluble lipid-nsL-TP complex is the key step in nsL-TP-mediated phospholipid transfer.

Animals↗

PubMed1962

Episome-mediated transfer of drug resistance in Enterobacteriaceae IV. Interactions between resistance transfer factor and F-factor in Escherichia coli K-12.

Watanabe, T. (Keio University, Tokyo, Japan) and T. Fukasawa. Episome-mediated transfer of drug resistance in Enterobacteriaceae. IV. Interactions between resistance transfer factor and F-factor in Escherichia coli K-12. J. Bacteriol. 83:727-735. 1962. - Resistance transfer factor (RTF) present in F(+) and F'(+) strains was found to suppress completely the transfer of F-factor, F', and host chromosomes. On the other hand, the presence of RTF in Hfr strains was found to reduce the frequencies of recombination to about 10(-2) of those in Hfr strains, regardless of the types of Hfr. RTF present in an F(+) strain with colicinogenic factor E(1) inhibited the transfer of the colicinogenic factor, whereas the transfer of colicinogenic factor I was not suppressed by RTF. A hypothesis that the genetic determinant of RTF controlling its "transfer system" is epistatic to that of F-factor is presented. It was also shown that F-factor present in recipients slightly suppresses the acceptance of RTF and that RTF present in recipients slightly reduces the acceptance of F-factor, F', and host chromosomes. On the other hand, the acceptance of RTF by recipients in which RTF is present was found to be about 1% of that in recipients without RTF.

Drug Resistance↗

PubMed1963

GENE TRANSFER BY F' STRAINS OF ESCHERICHIA COLI K-12. I. DELAY IN INITIATION OF CHROMOSOME TRANSFER.

Pittard, James (Yale University, New Haven, Conn.), John S. Loutit, and Edward A. Adelberg. Gene transfer by F' strains of Escherichia coli K-12. I. Delay in initiation of chromosome transfer. J. Bacteriol. 85:1394-1401. 1963.-Two different F' strains were found to transfer both F-merogenote and chromosomal markers to recipient strains. When zygotes having received different chromosomal markers from the male were selected, a high percentage of them were found to have also received F-merogenote markers under conditions in which the mating of more than one male cell with a single female cell was excluded. An analysis of the kinetics of zygote formation revealed that chromosomal markers began to be transferred from F' strains 8 to 10 min later than from their analogous Hfr strains. The rate of chromosome transfer is the same from both F' and Hfr strains, and the difference observed in kinetic experiments was shown not to be due to any difference between the sequence of chromosomal genes in the F' and Hfr strains. F' strains and Hfr strains showed no difference in ability to form specific pairs with female recipients shortly after mixing. The observed delay in the transfer of chromosomal markers from F' cells thus means that, after specific pair formation, F' cells take 8 to 10 min longer than Hfr cells to initiate chromosome transfer.

Chromosomes↗

PubMed1975

Experiments on egg transfer in the cow and ewe: dependence of conception rate on the transfer procedure and stage of the oestrous cycle.

The effects on embryo survival of procedures used in transferring eggs non-surgically were investigated in three experiments in ewes and heifers. In Exp. 1, two techniques for introducing eggs into the uterus through the cervix in heifers were compared; namely (i) deposition of the eggs high into the uterine horn or (ii) into the body of the uterus. Both methods were followed by inflation of the uterus with carbon dioxide. Out of a total of 34 heifers, only one became pregnant by the use of Method (i). Non-surgical egg tansfers early (Days 3 to 5) or later (Days 6 to 9) in the oestrous cycles of heifers were carried out in Exp. 2. Three transfer procedures were compared: (i) pipette transfer of an egg into the body of the uterus through the cervix (control), (ii) the control procedure performed under Fluothane anaesthesia, or (iii) followed by inflation of the uterus with carbon dioxide. Wide transfers carried out early in the cycle, pregnancies resulted in 1/10, 0/10 and 1/10 of the heifers in the control, carbon dioxide and Fluothane groups, respectively. With late transfers, 7/20, 1/10 and 8/20 heifers became pregnant in the respective treatment groups. This trend for pregnancy rate to be improved when late transfers were done in the control and Fluothane groups was significant only at the 10% level of probability when both groups were pooled. It was tentatively concluded, however, that non-surgical transfers of fertilized eggs to heifers may be best done during mid-cycle, after Day 6. Fluothane anaesthesia did not improve conception rate. Inflation of the uterus with carbon dioxide appeared to be deleterious when used at the mid-cycle stage in heifers. In Exp. 3, it was found that inflation of the ewe's uterus with carbon dioxide or nitrogen following the surgical thansfer of an egg did not affect the incidence of pregnancy. The introduction of 50 mul liquid Fluothane into the lumen of the uterus was embryotoxic.

Animals↗

PubMed2005

Telomere length of transferred lymphocytes correlates with in vivo persistence and tumor regression in melanoma patients receiving cell transfer therapy.

Recent studies have indicated that adoptive immunotherapy with autologous antitumor tumor-infiltrating lymphocytes (TILs) following nonmyeloablative chemotherapy mediates tumor regression in approximately 50% of treated patients with metastatic melanoma, and that tumor regression is correlated with the degree of persistence of adoptively transferred T cells in peripheral blood. These findings, which suggested that the proliferative potential of transferred T cells may play a role in clinical responses, led to the current studies in which telomere length as well as phenotypic markers expressed on the administered TILs were examined. TILs that were associated with objective clinical responses following adoptive transfer possessed a mean telomere length of 6.3 kb, whereas TILs that were not associated with significant clinical responses were significantly shorter, averaging 4.9 kb (p < 0.01). Furthermore, individual TIL-derived T cell clonotypes that persisted in vivo following adoptive cell transfer possessed telomeres that were longer than telomeres of T cell clonotypes that failed to persist (6.2 vs 4.5 kb, respectively; p < 0.001). Expression of the costimulatory molecule CD28 also appeared to be associated with long telomeres and T cell persistence. These results, indicating that the telomere length of transferred lymphocytes correlated with in vivo T cell persistence following adoptive transfer, and coupled with the previous observation that T cell persistence was associated with clinical responses in this adoptive immunotherapy trial, suggest that telomere length and the proliferative potential of the transferred T cells may play a significant role in mediating response to adoptive immunotherapy.

Base Sequence↗

PubMed1994

Congregation transfers its healthcare system. Franciscan Sisters of Little Falls list critical factors for a successful transfer of sponsorship.

In 1993 the Franciscan Sisters of Little Falls, MN, transferred ownership and sponsorship of their 12 healthcare facilities to Catholic Health Corporation of Omaha. The sisters had had two goals from the start of the process: To transfer the facilities to another Catholic system, and in such a way that both members of the religious institute and the facilities' personnel would "own" the decision To complete the transfer with minimal upheaval in facility operations The sisters accomplished both of these goals. They attribute their success to prayer and several critical factors. First, having pondered their healthcare ministry in light of their Franciscan tradition, the sisters decided that a larger system could better meet their facilities' needs. Second, they developed a set of criteria for the new sponsor, including the requirement that it be both Catholic and dedicated to rural healthcare. Third, the sisters became willing to take the risks a transfer involved for both their congregation and the 12 facilities. Fourth, the sisters clearly communicated their decision to everyone affected by it. Fifth, they sought the help of experts in making the transfer. Sixth, they worked hard to create trust, so that all involved--including those who would lose their jobs--took ownership of the transfer decision. After completion of the transfer, each of the facilities held a ritual celebrating the friendships and respect built over the long years the Franciscan Sisters were their sponsors. The sisters held their own ritual of commemoration. They continue their ministries in health, education, social services, and pastoral care.

Catholicism↗

PubMed1990

Adoptive transfer of CD8+ T cells from immune animals does not transfer immunity to blood stage Plasmodium yoelii malaria.

The malaria parasite, Plasmodium yoelii 17X, causes a self-limited, nonlethal infection characterized, in the blood stage, by preferential invasion of reticulocytes. Previous studies have suggested that immunity to the blood stage infection may be related to enhanced levels of class I MHC Ag on the parasitized reticulocyte surface and can be adoptively transferred to immunodeficient mice by immune CD8+ T cells in the absence of CD4+ T cells. To further examine the mechanisms of CD8+ T cell involvement in immunity to blood stage P. yoelii infection, we performed in vivo CD8 depletion and adoptive transfer experiments. Depletion of CD8+ T cells during primary blood stage infection in BALB/c mice did not diminish the ability of the mice to resolve their infections. Spleen cells from immune BALB/c and C57BL/10 mice were transferred to BALB/c-nu/nu and C57BL/10-nu/nu mice, respectively. The recipient mice were CD4 depleted in vivo to kill any transferred CD4+ T cells. The mice failed to control the infection. Populations of CD4-, CD8+ T cells were transferred from immune CBA/CaJ donors to in vivo CD4-depleted CBA/CaJ recipients. The mice were unable to control the infection. Although immune unfractionated spleen cells transferred rapid protection in all three mouse strains and immune CD4+ T cells transferred immunity in the two mouse strains studied, CD8+ T cells by themselves were neither protective nor did they enhance immunity.

Animals↗

PubMed1987

Transfer of recA protein from one polynucleotide to another. Kinetic evidence for a ternary intermediate during the transfer reaction.

We have analyzed the transfer kinetics of recA protein from one polynucleotide to another by monitoring the change in fluorescence of a modified single-stranded M13 DNA, referred to as etheno M13 DNA, that accompanies recA protein dissociation. The observed rate of transfer is dependent on the concentration of competitor polynucleotide, polythymidylic acid (poly(dT]; increasing the poly(dT) concentration increases the rate of transfer. These data are inconsistent with the rate-limiting step in the transfer mechanism occurring by a simple dissociation process. Under certain conditions, the apparent rate constant displays plateau behavior at high poly(dT) concentrations. This result is indicative of transfer occurring through a ternary intermediate including etheno M13 DNA and poly(dT). The transfer reaction was found to occur through two kinetically distinct species of transferring recA protein X DNA complexes. The relative amounts of these two species was affected by both the MgCl2 and protein concentration, suggesting that the two kinetic components reflect different aggregation states of the recA protein X DNA complex. Because etheno M13 DNA and poly(dT) contain no complementary sequences, we have concluded that recA protein has the intrinsic ability to form a kinetic ternary intermediate with two separate single-stranded DNA molecules in the absence of homology.

Adenosine Diphosphate↗

PubMed1981

Accelerated transfer of neutral glycosphingolipids and ganglioside GM1 by a purified lipid transfer protein.

The transfer of labeled neutral glycosphingolipids from sonicated phosphatidylcholine vesicles to erythrocyte ghosts is greatly stimulated by a nonspecific lipid transfer protein purified from beef liver. Globo-tetraglycosylceramide is transferred at a rate 40% of that for dipalmitoylphosphatidylcholine. II3-alpha-N-Acetylneuraminosyl-gangliotetraglycosylceramide is also transferred by the transfer protein, either from sonicated phosphatidylcholine vesicles or from ganglioside micelles to erythrocyte ghosts. The nonspecific lipid transfer protein catalyzes the net transfer of glycosphingolipids from brush border membrane vesicles (from rabbit intestine) to sonicated phosphatidylcholine/cholesterol vesicles.

Animals↗