#METABOLOMICS WORKBENCH theoissitt_20230331_063813 DATATRACK_ID:3830 STUDY_ID:ST002543 ANALYSIS_ID:AN004190 PROJECT_ID:PR001638
VERSION             	1
CREATED_ON             	April 6, 2023, 3:07 pm
#PROJECT
PR:PROJECT_TITLE                 	GC/MS analysis of hypoxic volatile metabolic markers in the MDA-MB-231 breast
PR:PROJECT_TITLE                 	cancer cell line
PR:PROJECT_SUMMARY               	Hypoxia in disease describes persistent low oxygen conditions, observed in a
PR:PROJECT_SUMMARY               	range of pathologies, including cancer. In the discovery of biomarkers in
PR:PROJECT_SUMMARY               	biological models, pathophysiological traits present a source of translatable
PR:PROJECT_SUMMARY               	metabolic products for the diagnosis of disease in humans. Part of the
PR:PROJECT_SUMMARY               	metabolome is represented by its volatile, gaseous fraction; the volatilome.
PR:PROJECT_SUMMARY               	Human volatile profiles, such as those found in breath, are able to diagnose
PR:PROJECT_SUMMARY               	disease, however accurate volatile biomarker discovery is required to target
PR:PROJECT_SUMMARY               	reliable biomarkers to develop new diagnostic tools. Using custom chambers to
PR:PROJECT_SUMMARY               	control oxygen levels and facilitate headspace sampling, the MDA-MB-231 breast
PR:PROJECT_SUMMARY               	cancer cell line was exposed to hypoxia (1% oxygen) for 24 hours. The
PR:PROJECT_SUMMARY               	maintenance of hypoxic conditions in the system was successfully validated over
PR:PROJECT_SUMMARY               	this time period. Targeted and ununtargeted gas chromatography mass spectrometry
PR:PROJECT_SUMMARY               	approaches revealed four significantly altered volatile organic compounds when
PR:PROJECT_SUMMARY               	compared to control cells. Three compounds were actively consumed by cells:
PR:PROJECT_SUMMARY               	methyl chloride, acetone and n-Hexane. Cells under hypoxia also produced
PR:PROJECT_SUMMARY               	significant amounts of styrene. This work presents a novel methodology for
PR:PROJECT_SUMMARY               	identification of volatile metabolisms under controlled gas conditions with
PR:PROJECT_SUMMARY               	novel observations of volatile metabolisms by breast cancer cells.
PR:INSTITUTE                     	University of York
PR:DEPARTMENT                    	Biology
PR:LAST_NAME                     	Issitt
PR:FIRST_NAME                    	Theo
PR:ADDRESS                       	Biology Dept. University of York
PR:EMAIL                         	ti538@york.ac.uk
PR:PHONE                         	07398244497
PR:FUNDING_SOURCE                	BBSRC
PR:PUBLICATIONS                  	T. Issitt et al., Volatile compounds in human breath: critical review and
PR:PUBLICATIONS                  	meta-analysis Journal of Breath Research, Volume 16, Number 2 (2022)
PR:PUBLICATIONS                  	https://iopscience.iop.org/article/10.1088/1752-7163/ac5230#jbrac5230s2
#STUDY
ST:STUDY_TITLE                   	GC/MS analysis of hypoxic volatile metabolic markers in the MDA-MB-231 breast
ST:STUDY_TITLE                   	cancer cell line
ST:STUDY_SUMMARY                 	Hypoxia in disease describes persistent low oxygen conditions, observed in a
ST:STUDY_SUMMARY                 	range of pathologies, including cancer. In the discovery of biomarkers in
ST:STUDY_SUMMARY                 	biological models, pathophysiological traits present a source of translatable
ST:STUDY_SUMMARY                 	metabolic products for the diagnosis of disease in humans. Part of the
ST:STUDY_SUMMARY                 	metabolome is represented by its volatile, gaseous fraction; the volatilome.
ST:STUDY_SUMMARY                 	Human volatile profiles, such as those found in breath, are able to diagnose
ST:STUDY_SUMMARY                 	disease, however accurate volatile biomarker discovery is required to target
ST:STUDY_SUMMARY                 	reliable biomarkers to develop new diagnostic tools. Using custom chambers to
ST:STUDY_SUMMARY                 	control oxygen levels and facilitate headspace sampling, the MDA-MB-231 breast
ST:STUDY_SUMMARY                 	cancer cell line was exposed to hypoxia (1% oxygen) for 24 hours. The
ST:STUDY_SUMMARY                 	maintenance of hypoxic conditions in the system was successfully validated over
ST:STUDY_SUMMARY                 	this time period. Targeted and untargeted gas chromatography mass spectrometry
ST:STUDY_SUMMARY                 	approaches revealed four significantly altered volatile organic compounds when
ST:STUDY_SUMMARY                 	compared to control cells. Three compounds were actively consumed by cells:
ST:STUDY_SUMMARY                 	methyl chloride, acetone and n-Hexane. Cells under hypoxia also produced
ST:STUDY_SUMMARY                 	significant amounts of styrene. This work presents a novel methodology for
ST:STUDY_SUMMARY                 	identification of volatile metabolisms under controlled gas conditions with
ST:STUDY_SUMMARY                 	novel observations of volatile metabolisms by breast cancer cells.
ST:INSTITUTE                     	University of York
ST:LAST_NAME                     	Issitt
ST:FIRST_NAME                    	Theo
ST:ADDRESS                       	Biology Dept. University of York, Personal
ST:EMAIL                         	ti538@york.ac.uk
ST:NUM_GROUPS                    	4
ST:PUBLICATIONS                  	T. Issitt et al., Volatile compounds in human breath: critical review and
ST:PUBLICATIONS                  	meta-analysis Journal of Breath Research, Volume 16, Number 2 (2022)
ST:PUBLICATIONS                  	https://iopscience.iop.org/article/10.1088/1752-7163/ac5230#jbrac5230s2
ST:PHONE                         	07398244497
#SUBJECT
SU:SUBJECT_TYPE                  	Cultured cells
SU:SUBJECT_SPECIES               	Homo sapiens
SU:TAXONOMY_ID                   	9606
SU:CELL_STRAIN_DETAILS           	MDA-MB-231
#SUBJECT_SAMPLE_FACTORS:         	SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Raw file names and additional sample data
SUBJECT_SAMPLE_FACTORS           	-	m1	Sample Type:Media | Treatment:Control	
SUBJECT_SAMPLE_FACTORS           	-	m2	Sample Type:Media | Treatment:Control	
SUBJECT_SAMPLE_FACTORS           	-	m3	Sample Type:Media | Treatment:Control	
SUBJECT_SAMPLE_FACTORS           	-	m4	Sample Type:Media | Treatment:Control	
SUBJECT_SAMPLE_FACTORS           	-	m5	Sample Type:Media | Treatment:Control	
SUBJECT_SAMPLE_FACTORS           	-	m6	Sample Type:Media | Treatment:Control	
SUBJECT_SAMPLE_FACTORS           	-	hm1	Sample Type:Media | Treatment:Hypoxia	
SUBJECT_SAMPLE_FACTORS           	-	hm2	Sample Type:Media | Treatment:Hypoxia	
SUBJECT_SAMPLE_FACTORS           	-	hm3	Sample Type:Media | Treatment:Hypoxia	
SUBJECT_SAMPLE_FACTORS           	-	hm4	Sample Type:Media | Treatment:Hypoxia	
SUBJECT_SAMPLE_FACTORS           	-	hm5	Sample Type:Media | Treatment:Hypoxia	
SUBJECT_SAMPLE_FACTORS           	-	hm6	Sample Type:Media | Treatment:Hypoxia	
SUBJECT_SAMPLE_FACTORS           	-	c1	Sample Type:Cells | Treatment:Control	
SUBJECT_SAMPLE_FACTORS           	-	c2	Sample Type:Cells | Treatment:Control	
SUBJECT_SAMPLE_FACTORS           	-	c3	Sample Type:Cells | Treatment:Control	
SUBJECT_SAMPLE_FACTORS           	-	c4	Sample Type:Cells | Treatment:Control	
SUBJECT_SAMPLE_FACTORS           	-	c5	Sample Type:Cells | Treatment:Control	
SUBJECT_SAMPLE_FACTORS           	-	c6	Sample Type:Cells | Treatment:Control	
SUBJECT_SAMPLE_FACTORS           	-	h1	Sample Type:Cells | Treatment:Hypoxia	
SUBJECT_SAMPLE_FACTORS           	-	h2	Sample Type:Cells | Treatment:Hypoxia	
SUBJECT_SAMPLE_FACTORS           	-	h3	Sample Type:Cells | Treatment:Hypoxia	
SUBJECT_SAMPLE_FACTORS           	-	h4	Sample Type:Cells | Treatment:Hypoxia	
SUBJECT_SAMPLE_FACTORS           	-	h5	Sample Type:Cells | Treatment:Hypoxia	
SUBJECT_SAMPLE_FACTORS           	-	h6	Sample Type:Cells | Treatment:Hypoxia	
#COLLECTION
CO:COLLECTION_SUMMARY            	Cells were placed in static headspace chambers as previously described [4] with
CO:COLLECTION_SUMMARY            	new, clean silicon gaskets. Low oxygen, hypoxic gas (1 % O2, 5 % CO2, 94 % N2;
CO:COLLECTION_SUMMARY            	purchased from BOC Specialty Gases, Woking, UK) was flushed through the chambers
CO:COLLECTION_SUMMARY            	at a rate of 4 L/min for 10 min (chamber volume = 25 L). Chambers were then
CO:COLLECTION_SUMMARY            	closed and placed at 37 ˚C for 2 hours to allow residual oxygen in the media to
CO:COLLECTION_SUMMARY            	equilibrate with chamber headspace. Chambers were then flushed again at a rate
CO:COLLECTION_SUMMARY            	of 4 L/min for 10 min, sealed and returned to 37 ˚C. After a further 24 hours,
CO:COLLECTION_SUMMARY            	chambers were flushed again at a rate of 4 L/min for 10 min. 15 ml of gas
CO:COLLECTION_SUMMARY            	standards (MeCl, 520 ppb (parts per billion); MeBr, 22 ppb; MeI, 26 ppb; DMS,
CO:COLLECTION_SUMMARY            	110 ppb; CFC-11, 400 ppb and CH3Cl3, 110ppb; BOC Specialty Gases, Woking, UK)
CO:COLLECTION_SUMMARY            	were then injected into the chambers through a butyl seal and time zero sample
CO:COLLECTION_SUMMARY            	taken. Injected compounds are either known metabolites for cancer cells, or
CO:COLLECTION_SUMMARY            	internal standards (CFC-11) for the analysis and quantification of metabolism.
CO:COLLECTION_SUMMARY            	Final chamber concentrations were similar to environmental concentrations, e.g
CO:COLLECTION_SUMMARY            	MeCl, 1.2 ppb and MeBr 0.05 ppb, particularly more polluted urban spaces
CO:COLLECTION_SUMMARY            	(Redeker et al., 2007). Injected gases are the same as those used for
CO:COLLECTION_SUMMARY            	calibration. Compounds not injected but detected at first time point, due to
CO:COLLECTION_SUMMARY            	residual presence from laboratory air, (including isoprene, acetone, 2-MP, 3-MP
CO:COLLECTION_SUMMARY            	and n-hexane) were quantified. Two time zero (T0) samples were taken using an
CO:COLLECTION_SUMMARY            	evacuated 500 mL electropolished stainless steel canister (LabCommerce, San
CO:COLLECTION_SUMMARY            	Jose, USA) through fine mesh Ascarite® traps (Archbold et al., 2005), after
CO:COLLECTION_SUMMARY            	which the chamber was resealed and left on a platform rocker on its slowest
CO:COLLECTION_SUMMARY            	setting for 120 min, at which point two further air samples (T1) were collected.
CO:COLLECTION_SUMMARY            	Duplicate samples were taken so that two analytical approaches could be
CO:COLLECTION_SUMMARY            	performed (targeted and non-untargeted MS). Cells were removed from the chamber,
CO:COLLECTION_SUMMARY            	washed with PBS twice and lysed in 500 µL RIPA buffer (NaCl (5 M), 5 mL
CO:COLLECTION_SUMMARY            	Tris-HCl (1 M, pH 8.0), 1 mL Nonidet P-40, 5 mL sodium deoxycholate (10 %), 1 mL
CO:COLLECTION_SUMMARY            	SDS (10 %)) with protease inhibitor (Sigma-Aldrich, Roche; Mannheim, Germany).
CO:COLLECTION_SUMMARY            	Protein concentration of lysates were determined using BCA assay (Thermo
CO:COLLECTION_SUMMARY            	Scientific, Waltham, MA, USA). Media alone was treated exactly the same as
CO:COLLECTION_SUMMARY            	cells, and only acetone was found to differ significantly between conditions
CO:COLLECTION_SUMMARY            	(Supplementary figure 1). These media blank outcomes were subtracted from
CO:COLLECTION_SUMMARY            	respective cellular samples prior to protein normalisation. Comparative controls
CO:COLLECTION_SUMMARY            	include lab air blanks and those data available from the dataset and collection
CO:COLLECTION_SUMMARY            	method published previously which created and quantified metabolic fluxes of
CO:COLLECTION_SUMMARY            	volatile compounds from MDA-MB-231 under hyperoxic (lab air) conditions (Issitt
CO:COLLECTION_SUMMARY            	et al., 2022a).
CO:SAMPLE_TYPE                   	Cultured cells
#TREATMENT
TR:TREATMENT_SUMMARY             	Cells were placed in static headspace chambers as previously described [4] with
TR:TREATMENT_SUMMARY             	new, clean silicon gaskets. Low oxygen, hypoxic gas (1 % O2, 5 % CO2, 94 % N2;
TR:TREATMENT_SUMMARY             	purchased from BOC Specialty Gases, Woking, UK) was flushed through the chambers
TR:TREATMENT_SUMMARY             	at a rate of 4 L/min for 10 min (chamber volume = 25 L). Chambers were then
TR:TREATMENT_SUMMARY             	closed and placed at 37 ˚C for 2 hours to allow residual oxygen in the media to
TR:TREATMENT_SUMMARY             	equilibrate with chamber headspace. Chambers were then flushed again at a rate
TR:TREATMENT_SUMMARY             	of 4 L/min for 10 min, sealed and returned to 37 ˚C. After a further 24 hours,
TR:TREATMENT_SUMMARY             	chambers were flushed again at a rate of 4 L/min for 10 min. 15 ml of gas
TR:TREATMENT_SUMMARY             	standards (MeCl, 520 ppb (parts per billion); MeBr, 22 ppb; MeI, 26 ppb; DMS,
TR:TREATMENT_SUMMARY             	110 ppb; CFC-11, 400 ppb and CH3Cl3, 110ppb; BOC Specialty Gases, Woking, UK)
TR:TREATMENT_SUMMARY             	were then injected into the chambers through a butyl seal and time zero sample
TR:TREATMENT_SUMMARY             	taken. Injected compounds are either known metabolites for cancer cells, or
TR:TREATMENT_SUMMARY             	internal standards (CFC-11) for the analysis and quantification of metabolism.
TR:TREATMENT_SUMMARY             	Final chamber concentrations were similar to environmental concentrations, e.g
TR:TREATMENT_SUMMARY             	MeCl, 1.2 ppb and MeBr 0.05 ppb, particularly more polluted urban spaces
TR:TREATMENT_SUMMARY             	(Redeker et al., 2007). Injected gases are the same as those used for
TR:TREATMENT_SUMMARY             	calibration. Compounds not injected but detected at first time point, due to
TR:TREATMENT_SUMMARY             	residual presence from laboratory air, (including isoprene, acetone, 2-MP, 3-MP
TR:TREATMENT_SUMMARY             	and n-hexane) were quantified. Two time zero (T0) samples were taken using an
TR:TREATMENT_SUMMARY             	evacuated 500 mL electropolished stainless steel canister (LabCommerce, San
TR:TREATMENT_SUMMARY             	Jose, USA) through fine mesh Ascarite® traps (Archbold et al., 2005), after
TR:TREATMENT_SUMMARY             	which the chamber was resealed and left on a platform rocker on its slowest
TR:TREATMENT_SUMMARY             	setting for 120 min, at which point two further air samples (T1) were collected.
TR:TREATMENT_SUMMARY             	Duplicate samples were taken so that two analytical approaches could be
TR:TREATMENT_SUMMARY             	performed (targeted and non-untargeted MS). Cells were removed from the chamber,
TR:TREATMENT_SUMMARY             	washed with PBS twice and lysed in 500 µL RIPA buffer (NaCl (5 M), 5 mL
TR:TREATMENT_SUMMARY             	Tris-HCl (1 M, pH 8.0), 1 mL Nonidet P-40, 5 mL sodium deoxycholate (10 %), 1 mL
TR:TREATMENT_SUMMARY             	SDS (10 %)) with protease inhibitor (Sigma-Aldrich, Roche; Mannheim, Germany).
TR:TREATMENT_SUMMARY             	Protein concentration of lysates were determined using BCA assay (Thermo
TR:TREATMENT_SUMMARY             	Scientific, Waltham, MA, USA). Media alone was treated exactly the same as
TR:TREATMENT_SUMMARY             	cells, and only acetone was found to differ significantly between conditions
TR:TREATMENT_SUMMARY             	(Supplementary figure 1). These media blank outcomes were subtracted from
TR:TREATMENT_SUMMARY             	respective cellular samples prior to protein normalisation. Comparative controls
TR:TREATMENT_SUMMARY             	include lab air blanks and those data available from the dataset and collection
TR:TREATMENT_SUMMARY             	method published previously which created and quantified metabolic fluxes of
TR:TREATMENT_SUMMARY             	volatile compounds from MDA-MB-231 under hyperoxic (lab air) conditions (Issitt
TR:TREATMENT_SUMMARY             	et al., 2022a).
TR:TREATMENT                     	Hypoxia
TR:TREATMENT_VEHICLE             	Nitrogen
TR:CELL_STORAGE                  	37 degrees
TR:CELL_MEDIA                    	DMEM
TR:CELL_ENVIR_COND               	Hypoxia/lab air
#SAMPLEPREP
SP:SAMPLEPREP_SUMMARY            	Collected canister samples were transferred to a liquid nitrogen trap through
SP:SAMPLEPREP_SUMMARY            	pressure differential. Pressure change between beginning and end of
SP:SAMPLEPREP_SUMMARY            	“injection” was measured, allowing calculation of the moles of canister
SP:SAMPLEPREP_SUMMARY            	collected air injected. Sample in the trap was then transferred, via heated
SP:SAMPLEPREP_SUMMARY            	helium flow, to an Aglient/HP 5972 MSD system (Santa Clara, CA, USA) equipped
SP:SAMPLEPREP_SUMMARY            	with a PoraBond Q column (25 m x 0.32 mm x 0.5 μm film thickness) (Restek©,
SP:SAMPLEPREP_SUMMARY            	Bellefonte, PN, USA). Targeted samples were analyzed in selected ion monitoring
SP:SAMPLEPREP_SUMMARY            	(SIM) mode, and untargeted samples in full scan (SCAN) mode with the mass range
SP:SAMPLEPREP_SUMMARY            	of 45-200 amu. The mass spectrometer was operated in electron impact ionization
SP:SAMPLEPREP_SUMMARY            	mode with 70 eV ionization energy, and transfer line, ion source, and quadrupole
SP:SAMPLEPREP_SUMMARY            	temperatures of 250, 280 and 280, respectively. For details on SIM and
SP:SAMPLEPREP_SUMMARY            	significantly altered, identified SCAN compounds, see Table 1. All samples were
SP:SAMPLEPREP_SUMMARY            	analysed within 6 days of collection. The oven program for both SIM and SCAN
SP:SAMPLEPREP_SUMMARY            	analyses were identical and are as follows: 35 ˚C for 2 min, 10 ˚C/min to 155
SP:SAMPLEPREP_SUMMARY            	˚C, 1 ˚C/min to 131 ˚C and 25 ˚C/min to 250 with a 5 min 30 second hold.
SP:SAMPLEPREP_SUMMARY            	Calibration was performed using standard gases (BOC Specialty Gases, Woking,
SP:SAMPLEPREP_SUMMARY            	UK). Linear regression of calibration curves confirmed strong, positive linear
SP:SAMPLEPREP_SUMMARY            	relationships between observed compound peak areas and moles of gas injected for
SP:SAMPLEPREP_SUMMARY            	each VOC (r2 > 0.9 in all cases). For compounds not purchased in gaseous state
SP:SAMPLEPREP_SUMMARY            	(BOC Specialty gases, as above), 1–2 mL of compound in liquid phase was
SP:SAMPLEPREP_SUMMARY            	injected neat into butyl sealed Wheaton-style glass vials (100 mL) and allowed
SP:SAMPLEPREP_SUMMARY            	to equilibrate for 1 h. 1 mL of headspace air was then removed from neat vial
SP:SAMPLEPREP_SUMMARY            	headspace using a gas tight syringe (Trajan, SGE) and injected into the
SP:SAMPLEPREP_SUMMARY            	headspace of a second 100 mL butyl sealed Wheaton-style glass vial. This was
SP:SAMPLEPREP_SUMMARY            	then repeated, and 1 mL of the 2nd serial dilution vial was injected into the
SP:SAMPLEPREP_SUMMARY            	GCMS system with 29 mL of lab air to give ppb concentrations. This was performed
SP:SAMPLEPREP_SUMMARY            	for methanethiol (MeSH (SPEXorganics, St Neots, UK)), isoprene (Alfa Aesar, Ward
SP:SAMPLEPREP_SUMMARY            	Hill, MA, USA), acetone (Sigma-Aldrich, Burlington, MA, USA), 2- & 3-methyl
SP:SAMPLEPREP_SUMMARY            	pentane and n-hexane (Thermo Scientific, Waltham, MA, USA). Reported compounds
SP:SAMPLEPREP_SUMMARY            	detected by the GC/-MS were confirmed by matching retention times and
SP:SAMPLEPREP_SUMMARY            	mass–charge (m/z) ratios with known standards.
SP:PROCESSING_STORAGE_CONDITIONS 	Room temperature
#CHROMATOGRAPHY
CH:CHROMATOGRAPHY_SUMMARY        	Collected canister samples were transferred to a liquid nitrogen trap through
CH:CHROMATOGRAPHY_SUMMARY        	pressure differential. Pressure change between beginning and end of
CH:CHROMATOGRAPHY_SUMMARY        	“injection” was measured, allowing calculation of the moles of canister
CH:CHROMATOGRAPHY_SUMMARY        	collected air injected. Sample in the trap was then transferred, via heated
CH:CHROMATOGRAPHY_SUMMARY        	helium flow, to an Aglient/HP 5972 MSD system (Santa Clara, CA, USA) equipped
CH:CHROMATOGRAPHY_SUMMARY        	with a PoraBond Q column (25 m x 0.32 mm x 0.5 μm film thickness) (Restek©,
CH:CHROMATOGRAPHY_SUMMARY        	Bellefonte, PN, USA). Targeted samples were analyzed in selected ion monitoring
CH:CHROMATOGRAPHY_SUMMARY        	(SIM) mode, and untargeted samples in full scan (SCAN) mode with the mass range
CH:CHROMATOGRAPHY_SUMMARY        	of 45-200 amu. The mass spectrometer was operated in electron impact ionization
CH:CHROMATOGRAPHY_SUMMARY        	mode with 70 eV ionization energy, and transfer line, ion source, and quadrupole
CH:CHROMATOGRAPHY_SUMMARY        	temperatures of 250, 280 and 280, respectively. For details on SIM and
CH:CHROMATOGRAPHY_SUMMARY        	significantly altered, identified SCAN compounds, see Table 1. All samples were
CH:CHROMATOGRAPHY_SUMMARY        	analysed within 6 days of collection. The oven program for both SIM and SCAN
CH:CHROMATOGRAPHY_SUMMARY        	analyses were identical and are as follows: 35 ˚C for 2 min, 10 ˚C/min to 155
CH:CHROMATOGRAPHY_SUMMARY        	˚C, 1 ˚C/min to 131 ˚C and 25 ˚C/min to 250 with a 5 min 30 second hold.
CH:CHROMATOGRAPHY_TYPE           	GC
CH:INSTRUMENT_NAME               	HP GCD 1800B
CH:COLUMN_NAME                   	Agilent PoraBOND Q (25m x 0.32mm x 0.5um)
CH:SOLVENT_A                     	NA
CH:SOLVENT_B                     	NA
CH:FLOW_GRADIENT                 	NA
CH:FLOW_RATE                     	10ml/min
CH:COLUMN_TEMPERATURE            	250
#ANALYSIS
AN:ANALYSIS_TYPE                 	MS
#MS
MS:INSTRUMENT_NAME               	Agilent/HP 5972 MSD
MS:INSTRUMENT_TYPE               	Single quadrupole
MS:MS_TYPE                       	EI
MS:ION_MODE                      	POSITIVE
MS:MS_COMMENTS                   	Calibration was performed using standard gases (BOC Specialty Gases, Woking,
MS:MS_COMMENTS                   	UK). Linear regression of calibration curves confirmed strong, positive linear
MS:MS_COMMENTS                   	relationships between observed compound peak areas and moles of gas injected for
MS:MS_COMMENTS                   	each VOC (r2 > 0.9 in all cases). For compounds not purchased in gaseous state
MS:MS_COMMENTS                   	(BOC Specialty gases, as above), 1–2 mL of compound in liquid phase was
MS:MS_COMMENTS                   	injected neat into butyl sealed Wheaton-style glass vials (100 mL) and allowed
MS:MS_COMMENTS                   	to equilibrate for 1 h. 1 mL of headspace air was then removed from neat vial
MS:MS_COMMENTS                   	headspace using a gas tight syringe (Trajan, SGE) and injected into the
MS:MS_COMMENTS                   	headspace of a second 100 mL butyl sealed Wheaton-style glass vial. This was
MS:MS_COMMENTS                   	then repeated, and 1 mL of the 2nd serial dilution vial was injected into the
MS:MS_COMMENTS                   	GCMS system with 29 mL of lab air to give ppb concentrations. This was performed
MS:MS_COMMENTS                   	for methanethiol (MeSH (SPEXorganics, St Neots, UK)), isoprene (Alfa Aesar, Ward
MS:MS_COMMENTS                   	Hill, MA, USA), acetone (Sigma-Aldrich, Burlington, MA, USA), 2- & 3-methyl
MS:MS_COMMENTS                   	pentane and n-hexane (Thermo Scientific, Waltham, MA, USA). Reported compounds
MS:MS_COMMENTS                   	detected by the GC/-MS were confirmed by matching retention times and
MS:MS_COMMENTS                   	mass–charge (m/z) ratios with known standards. Equation 1: [VOC](ppt)=(CF x
MS:MS_COMMENTS                   	〖10〗^12 x Peak area x Calibration slope)/n Equation 1 outlines the approach
MS:MS_COMMENTS                   	to calculating VOC concentrations in parts-per-trillion-by-volume, or pptv. Here
MS:MS_COMMENTS                   	Peak area refers to the combined peak areas for the mass-charge ratios
MS:MS_COMMENTS                   	identified in Table 1. Multiplying Peak areas by their associated calibration
MS:MS_COMMENTS                   	curves (Calibration Slope) generate molar amounts which, when divided by the
MS:MS_COMMENTS                   	number of moles of headspace air injected (n), generate a unitless (moles
MS:MS_COMMENTS                   	compound/moles of air) ratio. Pptv concentrations are then obtained by
MS:MS_COMMENTS                   	multiplying this unitless ratio by 1x1012. For clarity,
MS:MS_COMMENTS                   	part-per-billion-by-volume values would be obtained by multiplying the unitless
MS:MS_COMMENTS                   	ratios by 1x109, or one billion. Sample VOC concentrations were then normalised
MS:MS_COMMENTS                   	to CFC-11 concentrations (240 parts-per-trillion-by-volume (pptv)) through
MS:MS_COMMENTS                   	multiplication by a “correction factor”, or CF, Equation 1). CFC-11 was used
MS:MS_COMMENTS                   	as an internal standard, since atmospheric concentrations of CFC-11 are globally
MS:MS_COMMENTS                   	consistent and stable (Redeker et al., 2007). Quantification of Styrene was done
MS:MS_COMMENTS                   	as above but normalisation to CFC-11 was not possible under flushed, hypoxic
MS:MS_COMMENTS                   	conditions. NEGATIVE VALUES IN DATA SHOW CONSUMPTION OVER TIME. VARIATION IN
MS:MS_COMMENTS                   	SCALE BETWEEN MEDIA SAMPLES ARE DUE TO NORMALISATION OF CELLULAR DATA TO
MS:MS_COMMENTS                   	PROTEIN. AS DESCRIBED, MEDIA VALUES ARE SUBTRACTED FROM CELLULAR DATA PRIOR TO
MS:MS_COMMENTS                   	NORMALISATION AND EXPRESSED AS PG/HR/UG.
#MS_METABOLITE_DATA
MS_METABOLITE_DATA:UNITS	pg/hr/ug and g/hr for media
MS_METABOLITE_DATA_START
Samples	c1	c2	c3	c4	c5	c6	h1	h2	h3	h4	h5	h6	m1	m2	m3	m4	m5	m6	hm1	hm2	hm3	hm4	hm5	hm6
Factors	Sample Type:Cells | Treatment:Control	Sample Type:Cells | Treatment:Control	Sample Type:Cells | Treatment:Control	Sample Type:Cells | Treatment:Control	Sample Type:Cells | Treatment:Control	Sample Type:Cells | Treatment:Control	Sample Type:Cells | Treatment:Hypoxia	Sample Type:Cells | Treatment:Hypoxia	Sample Type:Cells | Treatment:Hypoxia	Sample Type:Cells | Treatment:Hypoxia	Sample Type:Cells | Treatment:Hypoxia	Sample Type:Cells | Treatment:Hypoxia	Sample Type:Media | Treatment:Control	Sample Type:Media | Treatment:Control	Sample Type:Media | Treatment:Control	Sample Type:Media | Treatment:Control	Sample Type:Media | Treatment:Control	Sample Type:Media | Treatment:Control	Sample Type:Media | Treatment:Hypoxia	Sample Type:Media | Treatment:Hypoxia	Sample Type:Media | Treatment:Hypoxia	Sample Type:Media | Treatment:Hypoxia	Sample Type:Media | Treatment:Hypoxia	Sample Type:Media | Treatment:Hypoxia
Methyl Chloride	2.61	1.72	3.1	0.412	0.246	0.159	2.56434	1.37297	3.4969	3.99687	1.46855	6.32169	-5.6E-11	1.95E-11	-3.2E-11	6E-10	1.49E-10	1.19E-09	-1.72E-09	1.49E-10	1.22E-09	-5.98E-10	3.74E-09	-1.59E-10
Methyl Bromide	0.0688	0.0374	0.164	-0.0044	-0.00218	0.0562	-0.32024	-0.21665	-0.4076	-0.68796	-0.25646	-0.35911	-3.1E-12	-5E-11	-1.6E-11	2.73E-11	2E-13	5.77E-11	5.2E-10	2E-13	-4.98E-11	5.19E-12	5.67E-11	-5.47E-11
Methyl Iodide	-0.25	-0.435	-0.0682	-0.294	-0.415	-0.898	-0.55367	-0.26582	-0.6111	-1.1995	-0.38518	0.368757	1.11E-09	4.23E-10	1.34E-09	3.59E-10	2.34E-10	3.38E-10	3.18E-10	2.34E-10	7.88E-11	1.92E-10	1.08E-11	-5.23E-12
Dimethyl Sulfide	0.323	0.242	0.625	0.354	0.0873	0.0747	0.20453	0.110079	0.22562	0.335932	0.141956	0.268028	-5.1E-11	1.84E-11	3.16E-11	5.27E-11	-2.9E-11	-3.4E-10	0	-2.9E-11	4.16E-11	-3.88E-11	-9.85E-10	-3.64E-09
Isoprene	0.428	0.32	-0.0481	-0.104	-0.154	0.118	0.481835	0.0738151	0.70204	-0.059799	0.441715	0.0932868	-2.3E-10	2.02E-11	9.96E-10	1.65E-10	-2.3E-09	1.57E-09	-4.71E-11	-2.3E-09	-1.89E-10	-1.55E-12	1.49E-10	2.09E-10
Chloroform	-0.104	-0.451	-0.101	-0.62	-0.412	-0.0302	2.30228	1.66244	1.8918	3.25423	1.19027	1.24022	-1.3E-10	4.51E-11	-2.5E-11	-7.4E-11	9.09E-11	-4.9E-10	-1.11E-11	9.09E-11	-6.24E-10	-1.62E-11	1.1E-09	-1.39E-09
Acetone	-49.9	116	-35.5	-7.34	-10.4	7.99	19.5694979	-65.161592	8.946913405	50.24965166	3.639117249	-5.562833308	0.000000104	0.000000106	8.23E-08	7.72425E-08	7.22105E-08	1.11894E-07	-9.21E-10	1.22E-09	1.87E-09	-2.08E-10	-9.91E-10	-2.71E-09
2 methyl pentane	1.13	0.0944	0.0303	-0.595	0.123	-0.0467	0.662050292	0.779027602	0.384966679	0.472956307	-0.121430636	-0.801541663	-1.01E-10	8.54E-10	-9E-11	5.66E-10	5.07E-10	5.21E-10	-4.25E-10	2.49E-10	-6.85E-09	-6.56E-10	3.39E-10	-2.31E-10
3 methyl pentane	-2	23.3	0.898	-0.138	-1.44	4.16	13.03386692	-5.978676072	0.903350139	-20.0137048	73.69060466	-3.332717179	3.99E-10	3.81E-09	3.38E-09	8.64E-10	-8.24E-11	-1.34E-09	-2.68E-09	1.67E-09	-6.4E-09	1.25E-09	1.98E-09	-3.58E-09
n-hexane	0.269	0.402	1.98	1.22	5.97	16.9	-53.0481823	-39.6221829	-39.4898174	-38.2154298	-62.07532572	-39.84857404	-6.82E-11	1.35E-09	-1.57E-09	2.66E-09	-1.39E-09	4.72E-11	-4.39E-09	1.82E-10	-3.15E-09	-1.46E-09	1.92E-10	1.75E-10
Styrene	ND	ND	ND	ND	ND	ND	3.34E-08	1.52E-08	8.6E-09	2.15E-08	1.23E-08	ND	ND	ND	ND	ND	ND	ND	3.48E-09	-4.03E-09	-2.2E-09	0	0	0
MS_METABOLITE_DATA_END
#METABOLITES
METABOLITES_START
metabolite_name	Pubchem ID
Methyl Chloride	6327
Methyl Bromide	6323
Methyl Iodide	6328
Dimethyl Sulfide	1068
Isoprene	6557
Chloroform	6212
Acetone	180
2 methyl pentane	7892
3 methyl pentane	7282
n-hexane	8058
Styrene	7501
METABOLITES_END
#END