MTtbox documentation
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Current Status
MTtbox is currently under test and further development
The main data structure is called: 'data'. It can be accessed from the Matlab command line by declaring data to be global.
global data
at any time. The following documentation will refer to fields in data. It also refers to the custom menu items by menu:name.
Graphical User Interface
1 A
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1 C
A project is saved by selecting: menu:File:Save as Having first saved a project a default Interaction Function is created by selecting Edit. A default project file contains lots of comments to provide help on how to develop the project. At present the Interaction Functions is not copied to the new project on each Save as command - this has to be done manually. |
(Comments are in green - this web version of the matlab file is created using webify_interaction_function('MT_Edinb_20120427.m')). The default file is largely a copy of MTtbox_BoilerPlate.txt which should be updated to reflect the latest ideas on how to build the function.
function data = MT_Edinb_20120427( data, before ) if nargin < 1, return; end % % % extract factors from structure for i=1:size( data.factorprops.Concentration,2) factname=lower(data.factorprops.Index2Name{i}); eval([[factname,'_p'],'=reshape(','data.factorprops.Concentration(:,i),[ data.cellprops.cellsize]);']); eval([[factname,'_i'],'=','data.factorprops.Name2Index.(factname);']); end % insert model in here % data=setupDiffusion(data,'Factorname','s_micplm','DiffK',[0.2,0.2],... % 'RegionLists',{{'cytoplasm','vacuole','cell_wall'},{'plasma_membrane','microtubules'}}); % data=setupDiffusion(data,'Factorname','id_micplm','DiffK',[0,0],... % 'RegionLists',{{'cytoplasm','vacuole','cell_wall'},{'plasma_membrane','microtubules'}}); % data.factorprops.DiffusionConst(:,1)=0.1; % This should be superceed by the above % data.factorprops.DiffusionConst(:,2)=0.05;% This should be superceed by the above if data.iterations<0 % insert initialisation code here - use Initialise button to jump to here % modify default cell specifications, etc. to modify how the cell volume is partitioned, e.g. % data.organelleprops.plasma_membrane.size=0.95; % fraction of longest dimension % data.organelleprops.cytoplasm.size=0.80; % data.organelleprops.vacuole.size=0.4; % data.organelleprops.microtubules.nuclspont=0.0012; % observed nucleations per square (cubic) micron per sec elseif data.iterations==0 % insert startup code here - use Restart button to jump to here %% setup MT size %if data.cellprops.cellsize(1)>25 % data=mtSETprops(data,'microtubules','size',0.01,'microtubules','growthrate',0.025); % data=mtSETprops(data,'microtubules','shrinkrate',0.005); %end else %id_micplm_p(:)=0; % clear %id_micplm_p(data.cellprops.Vol==data.organelleprops.cytoplasm.Label)=0.8; % set cytoplasm region to 1 %id_micplm_p(round(data.cellprops.cellsize(1)/3):end,:,:)=0; % then set right hand end back to zero %s_micplm_p(id_micplm_p>0.1)=0.1; %% limit spontaneous nucleation to a region specified by id_micplm_p % data.organelleprops.microtubules.nuclspont=id_micplm_p; %data.cellprops.colourType=0; % set to 1 if colour is to be specified by individual MT property %Work through all the microtubules updating properties depending on flags %Average number of MT's present is observed to be about 80 i.e. 80/300 square microns (say 1 micron thick %so ~0.25 per square (cubic) micron for i_MT=1:length(data.working.dyn.microtubules.Org) MT=data.working.dyn.microtubules.Org(i_MT); % MTtbox monitors ... % MT.Props.growthrate % MT.Props.shrinkrate % MT.Props.maxbend % MT.Props.maxAge % MT.Props.nuclspont % MT.Props.nuclonMT % Make changes here, i.e. % diffs=diff(MT.Verts).^2; % calculate length of MT % MTlength=sum(sqrt(sum(diffs')'))*data.cellprops.micronsPerVoxelEdge; % microns % if MTlength>0.5 % MT.Props.nuclonMT=min(1,0.4*MTlength); % observed approx. 0.007 per micron per sec % else % MT.Props.nuclonMT=0; % end %ageMT=data.working.CellAge;% seconds %maxAgeColour=20; %MT.Props.FaceColor=[max(0,min(1,1-ageMT/maxAgeColour)), 0.5, max(0,min(1,ageMT/maxAgeColour))]; % if MT.BoundPLM %&& MT.Growing % it must have hit the plasma_membrane and not aligned % MT.Props.shrinkrate=20; % force it to shrink to oblivion % fprintf(1,'MT(%d) Collided with PLM fastshrink\n',i_MT); % end % if MT.BoundMic %&& MT.Growing % it must have hit the plasma_membrane and not aligned % MT.Props.shrinkrate=20; % force it to shrink to oblivion % fprintf(1,'MT(%d) Collided with MT fastshrink\n',i_MT); % end % Keep the following % Clear flags from collision detector MT.BoundPLM=false; MT.BoundMic=false; MT.BoundVac=false; data.working.dyn.microtubules.Org(i_MT)=MT; end end % put factors back into structure for i=1:size( data.factorprops.Concentration,2) factname=lower(data.factorprops.Index2Name{i}); eval(['data.factorprops.Concentration(:,i)=',[factname,'_p(:);']]); end end % This space intentionally left blank. % Default factor parameters % Default organelle parameters % cell_wall.size =0.000000 % cell_wall.offset =0.500000 % cell_wall.micronthick =0.100000 % cell_wall.minvox =1.000000 % cell_wall.FaceColor =[1.000000,0.000000,1.000000,] % cell_wall.FaceAlpha =0.010000 % cell_wall.Label =-5.000000 % cell_wall.isLayer =1.000000 % cell_wall.Static =1.000000 % cell_wall.InUse =1.000000 %plasma_membrane.size =0.000000 %plasma_membrane.offset =0.500000 %plasma_membrane.micronthick =0.010000 %plasma_membrane.minvox =3.000000 %plasma_membrane.FaceColor =[1.000000,1.000000,0.000000,] %plasma_membrane.FaceAlpha =0.020000 %plasma_membrane.Label =-4.000000 %plasma_membrane.isLayer =1.000000 %plasma_membrane.Static =1.000000 %plasma_membrane.InUse =1.000000 % cytoplasm.size =0.000000 % cytoplasm.offset =0.500000 % cytoplasm.micronthick =1.000000 % cytoplasm.minvox =5.000000 % cytoplasm.FaceColor =[0.000000,1.000000,0.000000,] % cytoplasm.FaceAlpha =0.020000 % cytoplasm.Label =0.000000 % cytoplasm.isLayer =1.000000 % cytoplasm.Static =1.000000 % cytoplasm.InUse =1.000000 % microtubules.size =0.025000 % microtubules.minvoxel =3.000000 % microtubules.growthrate =0.100000 % microtubules.shrinkrate =0.010000 % microtubules.maxbend =40.000000 % microtubules.MaxAngle =20.000000 % microtubules.maxAge =0.000000 % microtubules.nuclspont =0.050000 % microtubules.nuclonMT =0.090000 % microtubules.probCatastrophe=0.300000 % microtubules.FaceColor =[0.000000,0.000000,1.000000,] % microtubules.FaceAlpha =0.400000 % microtubules.Label =-6.000000 % microtubules.isLayer =0.000000 % microtubules.Static =0.000000 % microtubules.InUse =1.000000 % Default cell parameters % cellprops.shape ='Sphere' % cellprops.sheetmodel =0 % cellprops.maxLengthMicrons=20 % cellprops.secondsPerStep =1 % cellprops.micronsPerVoxelEdge=0.800000 % cellprops.cubicMicronsPerVoxel=0.512000 % cellprops.cellsize =[25,25,25,] % cellprops.colourType =1 % cellprops.Vol =[-1,-1,-1,-1, ... ] % cellprops.Smooth ='None' % cellprops.dynamic ='microtubules'... % cellprops.bound_distance =5 % cellprops.collide_distance=10 % cellprops.% vacuole.Vol=struct % vacuole.EdgeVol=struct % cellprops.% cell_wall.Vol=struct % cell_wall.EdgeVol=struct % cellprops.% plasma_membrane.Vol=struct % plasma_membrane.EdgeVol=struct % cellprops.% cytoplasm.Vol=struct % cytoplasm.EdgeVol=struct % cytoplasm.Indexes=struct % cellprops.% Diameter.microtubules=struct % cellprops.% microtubules.Vol=struct % microtubules.Offsets=struct % cellprops.sheetPlaneNormal=[0,1,0,]
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