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4 protocols using cyanocobalamin

1

Inducing ER Stress in Breast Cancer Cells

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MB468 and MB468res-R8 cell lines were maintained in DMEM (Sigma-Aldrich, D0422) supplemented with 10% dialyzed FBS (Omega Scientific), 1.5 μM cyanocobalamin (vitamin B12), 4 mM L-glutamine, 100 μM L-cysteine (Fisher Scientific), and 100 μM L-methionine (Sigma-Aldrich). In the case of methionine-free media, 370 μM DL-homocysteine (Sigma-Aldrich) was added in the absence of methionine.
To induce ER stress, MB468 and MB468res-R8 cells were treated with the 1 μM thapsigargin (Sigma-Aldrich, T9033) for 4 h. To inhibit PERK activation, cells were treated with 1 μM GSK2656157 (Millipore Sigma, 5.04651.0001) 1 h before media switch or thapsigargin treatment and replaced in the new media.
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2

Quantitative Analysis of Vitamins

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Thiamine hydrochloride (98.5–101.5%), Riboflavin (98%), Nicotinamide (98%), D-biotin (99%), Folic acid (99%) and cyanocobalamin (99%) were purchased from Fisher (Germany). Vitamins B5 (Pantothenic acid) and B6 (Pyridoxine hydrochloride) were purchased from Chem-Lab (Zedelgem, Belgium) and Fluorochem (United Kingdom) respectively. HPLC grade methanol, acetonitrile, chloroform (≥99.9%, containing amylenes as stabilizer) and salts for preparing the buffer solution were supplied by Sigma-Aldrich (Steinheim, Germany). Water used throughout the analyses was from a Millipore system.
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3

Bacterial Growth Kinetics with Vitamins

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The strains carrying various expression vectors were grown overnight at 37 °C on LB-agar plates supplemented with 25 μg ml−1 kanamycin and 100 μg ml−1 ampicillin. M9 minimal medium (47.7 mM Na2HPO4 × 12H2O, 17.2 mM KH2PO4, 18.7 mM NH4Cl, 8.6 mM NaCl) was supplemented with 0.4% glycerol, 2 mM MgSO4, 0.1 mM CaCl2, 100 μg ml−1l-arginine, 25 μg ml−1 kanamycin and 100 μg ml−1 ampicillin. A single colony was picked and used to inoculate an M9-medium pre-culture supplemented with 50 μg ml−1l-methionine (Sigma-Aldrich). The pre-culture was grown ~24 h at 37 °C, shaking in tubes with gas-permeable lids (Cellstar), and then used to inoculate the assay medium in a 1:500 ratio. The assay medium was supplemented with 0.00001% l-arabinose (Sigma-Aldrich) and either 50 μg ml−1l-methionine, 0.01 nM, 1 nM and 5 nM cyano-cobalamin (Acros Organics), or 0.1 nM hydroxy-cobalamin (Sigma-Aldrich). Overall, 200 μl medium was added per well of a sterile 96 well plate (Cellstar). Plates were sealed with a sterile and gas-permeable foil (BreatheEasy, Diversified Biotech). The cultures were grown for 1000 min (1250 min for Cbi) in a BioTek Power Wave 340 plate reader at 37 °C, shaking. The OD600 was measured every 5 min at 600 nm. All experiments were conducted as technical triplicates from biological triplicate. The displayed growth curves are the averages of all nine curves.
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4

BtuF-Cobalamin Binding Affinity Assay

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25 nM of BtuF488 in 50 mM KPi, pH 7.5 and 150 mM NaCl solution was mixed with various concentrations of Cyano-cobalamin (Acros Organics), ranging from 1 nM to 3 µM, to determine the dissociation constant. The mixture was incubated for 5 min at 30 °C in a black polystyrene 96-well plate (Greiner) coated with bovine serum albumin (BSA, Roth), to reduce interactions of BtuF488 with the 96-well plate. The fluorescence intensity was then measured on a Spark 10 M microplate reader (TECAN) using an excitation wavelength of 485 nm (bandwidth 5) and an emission wavelength of 520 nm (bandwidth 10). The normalised decrease in fluorescence was plotted against the substrate concentration. The measurements were performed as biological duplicates each containing technical triplicates. The KD was derived by fitting the formula Y=1AEt+X+KdEt+X+Kd24*Et*X2 in GraphPad Prism (version 10.0.2).
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