Statistical evaluation of colocalization patterns in immunogold labeling experiments.

The ultrastructural localization of various antigens in a cell using antibodies conjugated to gold particles is a powerful instrument in biological research. However, statistical or stereological tools for testing the observed patterns for significant clustering or colocalization are missing. The paper presents a method for the quantitative analysis of single or multiple immunogold labeling patterns using interpoint distances and tests the method using experimental data. The clustering or colocalization of gold particles was detected using various characteristics of the distribution of distances between them. Pair correlation and cross-correlation functions were used for exploratory analysis; second order reduced K (or cross-K) functions were used for testing the statistical significance of observed events. Confidence intervals of function values were estimated by Monte Carlo simulations of the Poisson process for independent particles, and results were visualized in histograms. Furthermore, a suitability of K functions modified by censoring or weighting was tested. The reliability of the method was assessed by evaluating the labeling patterns of nascent DNA and several nuclear proteins with known functions in replication foci of HeLa cells. The results demonstrate that the method is a powerful tool in biological investigations for testing the statistical significance of observed clustering or colocalization patterns in immunogold labeling experiments.

[1]  M. DePamphilis,et al.  Mechanisms for Priming DNA Synthesis , 1996 .

[2]  B. D. Ripley,et al.  Statistical Inference for Spatial Processes: Preface , 1988 .

[3]  R Berezney,et al.  Mapping replicational sites in the eucaryotic cell nucleus , 1989, The Journal of cell biology.

[4]  T. Hughes,et al.  On the structure of replication and transcription factories , 1995, Journal of Cell Science.

[5]  D. Jackson,et al.  Replication factories and nuclear bodies: the ultrastructural characterization of replication sites during the cell cycle. , 1994, Journal of cell science.

[6]  C. Burd,et al.  hnRNP proteins and the biogenesis of mRNA. , 1993, Annual review of biochemistry.

[7]  D. Jackson,et al.  A cell-cycle-dependent DNA polymerase activity that replicates intact DNA in chromatin. , 1986, Journal of molecular biology.

[8]  Shoichiro Tanaka,et al.  Intracellular localization of human DNA polymerase alpha with monoclonal antibodies. , 1982, The Journal of biological chemistry.

[9]  H Nakamura,et al.  Structural organizations of replicon domains during DNA synthetic phase in the mammalian nucleus. , 1986, Experimental cell research.

[10]  J. Lewins Contribution to the Discussion , 1989 .

[11]  D. Jackson,et al.  Visualization of replication factories attached to a nucleoskeleton , 1993, Cell.

[12]  I. Roberts,et al.  Statistical analysis of the distribution of gold particles over antigen sites after immunogold labelling , 1997 .

[13]  P. Cook,et al.  Does transcription by RNA polymerase play a direct role in the initiation of replication? , 1994, Journal of cell science.

[14]  D. Stoyan,et al.  Stochastic Geometry and Its Applications , 1989 .

[15]  D. Jackson,et al.  A gentle method for preparing cyto- and nucleo-skeletons and associated chromatin. , 1988, Journal of cell science.

[16]  G. Blobel,et al.  Nopp 140 shuttles on tracks between nucleolus and cytoplasm , 1992, Cell.