The proteins absorbance is maximum at 280nm due to the presence of tyrosine and tryptophan residues.

The change in wavelength is related to methods used for protein assay that -in some of them- give color change which reflects on absorbance wavelength.

For 460nm: Trinitrobenzene sulfonate method gives as results a yellow color which absorbs at 460nm.

For 660nm: There is ready to use reagent for protein assay called Pierce 600nm (Thermo Fischer). This reagent used for protein assay at 600nm.

Due to the diversity and complexity of proteins you should take in consideration that the selection of a method for a particular protein assay depends on convenience, sensitivity required and the nature of interfering compounds that may be present.

Dear Sir. Concerning your issue about the absorbance (wavelength) for inhibition of protein denaturation. I think the following below link and the attached file may help you in your analysis:

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1868981/pdf/4088.pdf

Thanks

thanks to all

Dear student

Protein is a combination of the Elements. In my observe, there are two kind of elements Heavy and Light or Hot life and Cold life.

What is the Hot life?

All the alive factors in the environment who have a strong relationship with Sun, their gene structure belongs to heavy elements. same as Polar Bear. It moves in nature by Sun-light. So, my answer to you first lets to change the law about our life . Because there is cancer diseases today in human life which it goes grow-up very fast

By this new perspective, you have got two different protein or element combinations heavy and light. About analyzing and measurement it belongs to using the product in heavy life consumer sevices area or light one