The construction of a small-size, magnetic sector, single focusing mass spectrometer (He-MS) for the continuous, on-site monitoring of He isotope ratios (3He/4He) is described. Nier type, electron impact ion source is usually installed. The ion source is the same as those used in modified-VG5400 mass spectrometers in our laboratory, which simplifies the evaluation and/or investigation of the performance as well as trouble shooting. A split-type flight tube was designed for the simultaneous detection of both 3He and 4He. Because of the low 3He/4He ratio (10?5) of naturally occurring He, the beam intensity of 3He is much weaker than the 4He ion beam, 3He is measured with a secondary electron multiplier operated in the ion-counting mode, while measuring 4He involves the use of a Faraday cup (High Faraday in Fig. 4). In the VX-770 flight tube, the 3He ion beam passes a narrow collector slit (300?m in width) so as to separate 3He ions from interfering HD and H3 ions with a resolving power of 500, while 4He is introduced into the outer flight tube, which passes through the wider collector slit (900?m in width). In order to simultaneously obtain 3He and 4He signals, the position of the collector slit for 4He can be adjusted by means of a manipulator and the focal point of the 4He ion beam can be moved slightly by applying positive voltages to a pair of deflecting plates that are located in front of the collector slit. Another Faraday cup (Axial Faraday) can be inserted into the 3He beam line to measure a strong ion beam such as 20Ne+ and 40Ar+ (Fig. 4). Fig.?4.?Design drawing of the He-MS instrument, consisting of the ion source, Q-lens, flight-tube, and collectors. High and axial Faraday mean the Faraday cup for 4He (high GP-IB, and then converted to imaginal voltage for convenience by the following formula, Fig.?5.?Schematic diagram of ion detectors and signal processing. Output signals of high and axial Faraday and ion counting are acquired by a computer through a GP-IB interface. where is an elementary charge (1.610?19 VX-770 C), counting rate (cps), and imaginal electric register Rabbit Polyclonal to RAB38 (11015 ). The intense 4He beam is usually collected in the Faraday cup and measured as a current mode by converting to voltage through an operational amplifier (OPA104CM: Burr-Brown Co.) with a 1.01010 feedback register (RHA2B: Hydragin Co.). The output voltage is measured using a digital multimeter (HP 34401: Agilent Technologies) and read by the computer GP-IB. Data acquisition is VX-770 usually carried out using the HP-Basic program reported by Nagao et al.15) and Sumino et al.16) A pair of electrodes (deflectors in Figs. 4 and 5) is usually installed in front of the collector slit for 4He, which functions as a zoom lens as well as a deflector of the 4He ion beam to focus the ion beam at the collector slit and to produce a flat top mass spectrum. Results and Evaluation of the He-MS Mass resolution, sensitivity, and detection limit VX-770 The basic specification of He-MS are summarized in Table 1, and the current instrument is compared with the miniature and conventional mass spectrometers for noble gas measurements developed by Sano et al.12) and the Modified-VG5400 installed at the University of Tokyo. Vacuum conditions, 5% valleys of the mass resolutions, sensitivities for 4He, background peak heights of HD, detection limits for 3He, and dynamic ranges of He detection, respectively, are listed. The mass resolution power is usually 430 for a 5% peak height (upper panel in Fig. 6), which is lower than the simulated value of 700 (Fig..
Tag Archives: VX-770
Protein synthesis rates are commonly measured by using isotopic tracers to
Protein synthesis rates are commonly measured by using isotopic tracers to quantify the VX-770 incorporation of a labelled amino acid into muscle proteins. SUnSET technique and then describe our SUnSET methodology and the evidence that supports the validity and accuracy of this technique for measuring skeletal muscle protein synthesis For many years puromycin has been an important tool in molecular biology by acting as a selection agent for cultured cells that express the enzyme puromycin-N-acetyl-transferase (33). Importantly puromycin is a structural analogue of aminoacyl-transfer RNA (aminoacyl-tRNA; specifically tyrosyl-tRNA; Figure 1A) and as such can be incorporated into elongating peptide chains via the formation of a peptide bond (23). However whereas aminoacyl-tRNAs VX-770 contain a hydrolyzable ester bond between their tRNA ribose moiety and the attached amino acid molecule puromycin has a non-hydrolyzable amide bond in the equivalent position (Figure 1A). Thus the binding of puromycin to a growing peptide chain prevents a new peptide bond from being formed with the next aminoacyl-tRNA. As a consequence puromycin binding results in the termination of peptide elongation and leads to the release of the truncated puromycin bound peptide from the ribosome (Figure 1B) (34). At very high concentrations puromycin effectively shuts down the elongation phase of translation and thus inhibit protein synthesis (35); however at very low concentrations that do not inhibit the overall rate of translation the rate at which puromycin-labelled peptides are formed reflects the overall rate of protein synthesis (29). This later property makes puromycin a potential tool for the measurement of changes in protein synthesis rates. Indeed Nakano and Hara (1979) were the first to investigate the use of 3H-puromycin to measure changes in protein synthesis rates and demonstrated that puromycin could be used to effectively detect starvation- and low protein diet-induced decreases in protein synthesis rates in whole tissues including skeletal muscle (22). However it took another 30 years with the development of the SUnSET technique (29) to renew interest in the use of puromycin for detecting changes in protein synthesis. Figure 1 Puromycin structure and mechanism of action SUnSET The SUnSET or SUrface SEnsing of Translation technique specifically involves the use of an anti-puromycin antibody for the immunological detection Rabbit Polyclonal to Chk2 (phospho-Thr68). of puromycin-labelled VX-770 peptides (29). Originally developed for use in cultured cells SUnSET allows for the detection of changes in protein synthesis in whole cell lysates using western blotting (WB) in multiple live cells using fluorescence-activated cell sorting (FACS) and at the single cell level with immunohistochemistry (IHC) (29). SUnSET in cell culture has been shown to have a similar dynamic range as protein synthesis measurements performed using 35S-methionine. VX-770 Furthermore the dose of puromycin used in these cell culture studies (up to 18.4 μM) was shown to not interfere with the overall rate of protein synthesis (29). Importantly SUnSET is able to detect increases and decreases in protein synthesis that are essentially indistinguishable from those obtained using 35S-methionine (29). Thus SUnSET has been shown to be a valid alternative to the use of radioisotopes for measuring changes in protein synthesis in cell culture and provides a clear advantage in allowing for the visualization of protein synthesis at the single cell level (13 29 Using SUnSET to Measure Changes in Skeletal Muscle Protein Synthesis Due to our ongoing interest in the regulation of skeletal muscle mass and specifically the role of the mammalian target of rapamycin (mTOR) in regulating protein synthesis and muscle hypertrophy (8 15 we were very interested in determining if SUnSET could be used to detect changes in protein synthesis in whole skeletal muscles under conditions. Thus to investigate the validity and accuracy of the SUnSET technique we performed a number of experiments using WB and IHC to measure changes in protein synthesis rates at the whole muscle and single muscle fiber levels (10). Western Blot SUnSET First we set out to determine whether the VX-770 WB version of SUnSET (WB-SUnSET) could be used to detect an increase in protein synthesis induced by bilateral synergist ablation (SA) surgery and whether this increase would be similar to that detected using a traditional radioactive technique. To accomplish this mice were subjected to SA or sham surgeries and after 7 days the plantaris muscles were extracted and then incubated in an VX-770 bath for 30 min with.